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Results for "

Na

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Na+/Ca2+ Exchanger (11) Na+/H+ Exchanger (NHE) (14) Na+/HCO3- Cotransporter (1) Na+/K+ ATPase (36) NKCC (8) Sodium Channel (65) 5-HT Receptor (2) Adrenergic Receptor (7) Akt (1) Amyloid-β (2) Angiotensin Receptor (3) Antibiotic (4) Apical Sodium-Dependent Bile Acid Transporter (1) Apoptosis (20) ASCT (1) Atg8/LC3 (1) Autophagy (26) Bacterial (10) Beclin1 (1) Biochemical Assay Reagents (8) Calcium Channel (10) Calmodulin (1) Cholinesterase (ChE) (1) COX (4) Dopamine Receptor (2) EBV (1) Elastase (1) Endogenous Metabolite (15) Enteropeptidase (1) ERK (1) Fluorescent Dye (4) Fungal (5) G protein-coupled Bile Acid Receptor 1 (2) GABA Receptor (8) Glucosidase (5) GlyT (2) GPR109A (1) Guanylate Cyclase (1) HDAC (1) HIV (4) HSV (2) iGluR (3) IKK (2) Imidazoline Receptor (4) Indoleamine 2,3-Dioxygenase (IDO) (1) Influenza Virus (18) IRAK (2) Isotope-Labeled Compounds (8) Liposome (1) LXR (1) LYTACs (1) mAChR (2) Melanocortin Receptor (1) Mineralocorticoid Receptor (1) Mitochondrial Metabolism (3) Mitophagy (3) nAChR (1) NF-κB (9) NO Synthase (3) Parasite (3) Phosphodiesterase (PDE) (3) PKD (1) Potassium Channel (16) Prostaglandin Receptor (2) PROTAC Linkers (1) Proton Pump (4) RSV (1) SARS-CoV (1) Serotonin Transporter (2) SGLT (2) Src (2) Thrombin (1) Thyroid Hormone Receptor (1) TRP Channel (2) Virus Protease (4) Wnt (2)
By Research Areas:	Cancer (60) Cardiovascular Disease (47) Endocrinology (5) Infection (30) Inflammation/Immunology (31) Metabolic Disease (54) Neurological Disease (76)

By Targets:

Na+/Ca2+ Exchanger (11)

Na+/H+ Exchanger (NHE) (14)

Na+/HCO3- Cotransporter (1)

Na+/K+ ATPase (36)

NKCC (8)

Sodium Channel (65)

5-HT Receptor (2)

Adrenergic Receptor (7)

Akt (1)

Amyloid-β (2)

Angiotensin Receptor (3)

Antibiotic (4)

Apical Sodium-Dependent Bile Acid Transporter (1)

Apoptosis (20)

ASCT (1)

Atg8/LC3 (1)

Autophagy (26)

Bacterial (10)

Beclin1 (1)

Biochemical Assay Reagents (8)

Calcium Channel (10)

Calmodulin (1)

Cholinesterase (ChE) (1)

COX (4)

Dopamine Receptor (2)

EBV (1)

Elastase (1)

Endogenous Metabolite (15)

Enteropeptidase (1)

ERK (1)

Fluorescent Dye (4)

Fungal (5)

G protein-coupled Bile Acid Receptor 1 (2)

GABA Receptor (8)

Glucosidase (5)

GlyT (2)

GPR109A (1)

Guanylate Cyclase (1)

HDAC (1)

HIV (4)

HSV (2)

iGluR (3)

IKK (2)

Imidazoline Receptor (4)

Indoleamine 2,3-Dioxygenase (IDO) (1)

Influenza Virus (18)

IRAK (2)

Isotope-Labeled Compounds (8)

Liposome (1)

LXR (1)

LYTACs (1)

mAChR (2)

Melanocortin Receptor (1)

Mineralocorticoid Receptor (1)

Mitochondrial Metabolism (3)

Mitophagy (3)

nAChR (1)

NF-κB (9)

NO Synthase (3)

Parasite (3)

Phosphodiesterase (PDE) (3)

PKD (1)

Potassium Channel (16)

Prostaglandin Receptor (2)

PROTAC Linkers (1)

Proton Pump (4)

RSV (1)

SARS-CoV (1)

Serotonin Transporter (2)

SGLT (2)

Src (2)

Thrombin (1)

Thyroid Hormone Receptor (1)

TRP Channel (2)

Virus Protease (4)

Wnt (2)

By Research Areas:

Cancer (60)

Cardiovascular Disease (47)

Endocrinology (5)

Infection (30)

Inflammation/Immunology (31)

Metabolic Disease (54)

Neurological Disease (76)

256

Inhibitors & Agonists

Screening Libraries

Fluorescent Dye

Biochemical Assay Reagents

Peptides

MCE Kits

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

Ambroxol 2 Publications Verification Na-872	Glucosidase Autophagy	Neurological Disease Metabolic Disease
Ambroxol (NA-872), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research .

Ambroxol hydrochloride 2 Publications Verification Na-872 hydrochloride	Glucosidase Autophagy	Neurological Disease Metabolic Disease
Ambroxol hydrochloride (NA-872 hydrochloride), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol hydrochloride is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol hydrochloride induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research .

NA-184	Others	Neurological Disease
NA-184 is a selective calpain-2 inhibitor. NA-184 inhibits TBI-induced cell death with an EC₅₀ of 0.13 mg/kg .

NA2 Glycan	Others	Others
NA2 Glycan is NA2 N-linked oligosaccharide. NA2 is the asialo-substructure of A2 glycan. NA2 glycan can be isolated from mammalian serum glycoproteins, such as serum IgG .

NA-1-157	Bacterial	Infection Inflammation/Immunology
NA-1-157 is a potent irreversible covalent inhibitor of the GES-5 carbapenemase, with a MIC of 0.5 μg/mL .

Ambroxol hydrochloride (Standard) Na-872 hydrochloride (Standard)	Glucosidase Autophagy	Neurological Disease Metabolic Disease
Ambroxol (hydrochloride) (Standard) is the analytical standard of Ambroxol (hydrochloride). This product is intended for research and analytical applications. Ambroxol hydrochloride (NA-872 hydrochloride), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol hydrochloride is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol hydrochloride induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research .

Ambroxol (acefylline) Na-872 (acefylline); Acebrophylline	Glucosidase Autophagy	Neurological Disease Metabolic Disease
Ambroxol (NA-872) acefylline, an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol acefylline is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol acefylline induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research .

Ambroxol-d5 hydrochloride Na-872-d₅ hydrochloride	Isotope-Labeled Compounds Glucosidase Autophagy	Neurological Disease Metabolic Disease
Ambroxol-d₅ (hydrochloride) is the deuterium labeled Ambroxol hydrochloride. Ambroxol hydrochloride (NA-872 hydrochloride), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol hydrochloride is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol hydrochloride induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research[1][2].

N-Arachidonylglycine Na-Gly	GlyT Endogenous Metabolite	Inflammation/Immunology
N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endocannabinoid anandamide (AEA), is a GPR18 agonist (EC₅₀ = 44.5 nM). Unlike AEA, N-Arachidonylglycine has no activity at either CB1 or CB2 receptors. N-Arachidonylglycine inhibits GLYT2 (IC₅₀ = 5.1 μM). N-Arachidonylglycine also is an effective activator of endometrial cell migration .

Tat-NR2B9c 5+ Cited Publications Tat-NR2Bct; Na-1	iGluR NO Synthase	Neurological Disease
Tat-NR2B9c (Tat-NR2Bct; NA-1) is a postsynaptic density-95 (PSD-95) inhibitor, with EC₅₀ values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B binding to PSD-95 with IC₅₀ values of 0.5 μM and 8 μM, respectively. Tat-NR2B9c also inhibits neuronal nitric oxide synthase (nNOS)/PSD-95 interaction, and possesses neuroprotective efficacy .

Nav1.8-IN-1	Sodium Channel	Neurological Disease Inflammation/Immunology
Nav1.8-IN-1 (Compound 31) is a potent inhibitor of Na(v)1.8 sodium channel. Nav1.8-IN-1 has the potential for the research of inflammatory and neuropathic pain .

Tat-NR2B9c TFA 5+ Cited Publications Tat-NR2Bct TFA; Na-1 TFA	iGluR NO Synthase	Neurological Disease
Tat-NR2B9c TFA (Tat-NR2Bct TFA) is a postsynaptic density-95 (PSD-95) inhibitor, with EC₅₀ values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c TFA disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B binding to PSD-95 with IC₅₀ values of 0.5 μM and 8 μM, respectively. Tat-NR2B9c TFA also inhibits neuronal nitric oxide synthase (nNOS)/PSD-95 interaction, and possesses neuroprotective efficacy .

Nav1.7 blocker 1	Sodium Channel	Neurological Disease Inflammation/Immunology
Nav1.7 blocker 1 (example 41) is a Na ⁺ channel (Na_v) blocker with an IC₅₀ value of 0.037 μM. Nav1.7 blocker 1 can be used for the study of pain, including neuropathic pain, postoperative pain, inflammatory pain, and so on .

Nav1.7-IN-13	Sodium Channel	Neurological Disease
Nav1.7-IN-13 (compound 3g) is a sodium channel inhibitor that significantly inhibits Veratridine (HY-N6691)-induced neuronal activity. Nav1.7-IN-13 inhibits total Na+ current in DRG neurons in a concentration-dependent manner; slows down the activation of Navs. Nav1.7-IN-13 significantly alleviated mechanical pain behavior in a rat model of nerve injury (SNI) and had analgesic activity .

Chloroprocaine hydrochloride 2-Chloroprocaine hydrochloride	Na+/K+ ATPase	Neurological Disease
Chloroprocaine hydrochloride (2-Chloroprocaine hydrochloride) is a potent inhibitor of *Na,K-ATPase* activity with an IC₅₀ of 13 mM. Chloroprocaine hydrochloride blocks peripheral nerve .

5-HT/NA Reuptake inhibitor-1	5-HT Receptor Others	Neurological Disease
5-HT/NA Reuptake inhibitor-1 (compound 9) is a selective dual 5-HT and NA reuptake inhibitor with IC₅₀ of 660 nM and 70 nM respectively. . 5-HT/NA Reuptake inhibitor-1 has good in vitro human metabolic stability, hERG selectivity and passive membrane permeability .

Fmoc-NH-pentanoic acid-NHS-SO3Na	PROTAC Linkers	Cancer
Fmoc-NH-pentanoic acid-NHS-SO3Na is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .

CEF19, Epstein-Barr Virus latent NA-3A (458-466)	EBV	Inflammation/Immunology
CEF19, Epstein-Barr Virus latent NA-3A (458-466) is a single peptide epitope, YPLHEQHGM, representing residues 458-466 of the type 1 Epstein-Barr Virus (EBV) nuclear antigen 3A protein (B95.8 strain). CEF19, Epstein-Barr Virus latent NA-3A (458-466) can significantly affect cytotoxic T-lymphocyte (CTL) recognition .

Neuraminidase-IN-11	Influenza Virus	Infection
Neuraminidase-IN-11 (15e) is a potent and selective neuraminidase (NA) inhibitor with the IC₅₀ values of 4.7 nM, 8.46 nM and 1.5 nM against H1N1, H5N1 and H5N8 NAs respectively .

Sodium carboxymethyl cellulose (MW 250000) 5+ Cited Publications CMC-Na (MW 250000); CMC-Na (Viscosity:1500-3100 mPa.s)	Biochemical Assay Reagents	Others
Sodium carboxymethyl cellulose (CMC-Na) (MW 250000) is a sodium salt of carboxymethyl cellulose. Sodium carboxymethyl cellulose has adsorption and corrosion inhibition on low-carbon steel in an acidic medium. Sodium carboxymethyl cellulose can be used as a thickener, paste and barrier agent .

1-Naphthyl PP1 hydrochloride 1 Publications Verification 1-Na-PP 1 hydrochloride	Src	Cancer
1-Naphthyl PP1 hydrochloride (1-NA-PP 1 hydrochloride) is a selective inhibitor of src family kinases. 1-Naphthyl PP1 hydrochloride inhibits v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with IC₅₀s of 1.0, 0.6, 0.6, 18 and 22 μM, respectively .

1-Naphthyl PP1 1 Publications Verification 1-Na-PP 1	Src PKD	Cancer
1-Naphthyl PP1 (1-NA-PP 1) is a selective inhibitor of src family kinases and Protein Kinase D. 1-Naphthyl PP1 inhibits v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with IC₅₀s of 1.0, 0.6, 0.6, 18 and 22 μM, respectively .

Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide GD4K-Na	Enteropeptidase	Others
Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide (GD4K-na) is a substrate for human enteropeptidase (K_m: 0.16 mM) .

SBFI-AM	Fluorescent Dye	Others
SBFI-AM is a Na ⁺ selective fluorescent indicator. SBFI-AM shows selectivity for Na ⁺ over K ⁺ .

N-Bromoacetamide	Potassium Channel Sodium Channel	Others
N-Bromoacetamide can irreversibly remove sodium channel inactivation in the cytoplasmic face of the membrane, also decreasing K current rapid inactivation .

TAPS sodium TAPS Na	Biochemical Assay Reagents	Others
TAPS sodium is a biological buffer that protects the structural integrity of lysozyme bacteria and prevents them from thermal denaturation at high temperatures. A pKa of 8.1 for TAPS results in half-maximal connexin channel activity .

SM-6586	Calcium Channel Na+/Ca2+ Exchanger	Cardiovascular Disease
SM-6586 is a calcium channel antagonist and inhibitor of Na ⁺/H ⁺ and Na ⁺/Ca ²⁺ exchange transport, potentially for the treatment of cerebrovasular diseases and hypertension.

Vincanol (-)-IsoeburNamine; (-)-epi-EburNamine	Sodium Channel	Neurological Disease
Vincanol ((-)-Isoeburnamine) is a blocker of voltage-gated Na+ channels. Vincanol blocks Na ⁺ currents with an IC₅₀ value of 40 μM. Vincanol has neuroprotective effect .

CGP37157 3 Publications Verification	Na+/Ca2+ Exchanger	Neurological Disease Cancer
CGP37157 is a potent, selective inhibitor of Na ⁺/Ca ²⁺ exchanger, inhibiting the Na ⁺-induced Ca ²⁺-release from guinea-pig heart mitochondria, with an IC₅₀ of 0.8 μM.

Neuraminidase-IN-18	Influenza Virus	Infection
Neuraminidase-IN-18 (compound N5) is a novel polyheterocyclic neuraminidase (NA) inhibitor. Neuraminidase-IN-18 shows potency in inhibition of H5N1 NA with an IC₅₀ of 0.14 μM and 0.27 μM against the wild-type H5N1 NA and H5N1-H274Y mutant NA, respectively. Neuraminidase-IN-18 inhibits influenza virus replication by binding to NAs in cell level .

SEA0400 15+ Cited Publications	Na+/Ca2+ Exchanger	Cardiovascular Disease
SEA0400 is a novel and selective inhibitor of the Na ⁺-Ca ²⁺ exchanger (NCX), inhibiting Na ⁺-dependent Ca ²⁺ uptake in cultured neurons, astrocytes, and microglia with IC₅₀s of from 5 to 33 nM.

SBFI Sodium-binding benzofuran isophthalate	Fluorescent Dye	Others
SBFI is a membrane-permeant, fluorescent Na ⁺ indicator dye. SBFI is excited at 340 nm and the fluorophore emission is collected at 450 nm . SBFI selective for Na ⁺ over K ⁺ with K_d values of 20 and 120 mM for these ions, respectively. .

Laninamivir 2 Publications Verification R 125489	Influenza Virus	Infection
Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with IC₅₀s of 0.90 nM, 1.83 nM and 3.12 nM for avian H12N5 NA (N5), pH1N1 N1 NA (p09N1) and A/RI/5+/1957 H2N2 N2 (p57N2), respectively .

Cariporide 5 Publications Verification HOE-642 Free Base	Na+/H+ Exchanger (NHE)	Cardiovascular Disease Inflammation/Immunology Cancer
Cariporide (HOE-642) is a selective Na ⁺/H ⁺ exchange inhibitor.

Eniporide hydrochloride 1 Publications Verification EMD-96785 hydrochloride	Na+/H+ Exchanger (NHE)	Cardiovascular Disease
Eniporide hydrochloride (EMD-96785 hydrochloride) is a potent Na ⁺/H ⁺ exchange inhibitor.

S-8921	Apical Sodium-Dependent Bile Acid Transporter	Metabolic Disease
S-8921 is an ileal Na ⁺/bile acid cotransporter (IBAT) inhibitor.

Peramivir trihydrate 5+ Cited Publications RWJ 270201 trihydrate; BCX 1812 trihydrate	Influenza Virus	Infection
Peramivir trihydrate (RWJ-270201 trihydrate;BCX-1812 trihydrate) is a highly potent, selective and orally active influenza virus neuraminidase (NA) inhibitor, with IC₅₀ values ranging from 0.9 to 4.3 nM for nine NA subtypes .

Digoxigenin monodigitoxoside	Na+/K+ ATPase	Metabolic Disease
Digoxigenin monodigitoxoside is a Na+/K+ ATPase inhibitor and cardiac glycoside metabolite of digoxin.

Dronedarone Hydrochloride	Potassium Channel Autophagy	Cardiovascular Disease
Dronedarone Hydrochloride is a non-iodinated amiodarone derivative that inhibits Na ⁺, K ⁺ and Ca ²⁺ currents.

Ouabain Octahydrate 15+ Cited Publications Acocantherine; G-Strophanthin	Na+/K+ ATPase Autophagy	Cardiovascular Disease Cancer
Ouabain Octahydrate is an inhibitor of Na ⁺/K ⁺-ATPase, used for the treatment of congestive heart failure.

Oleandrin 2 Publications Verification PBI-05204	Na+/K+ ATPase	Cancer
Oleandrin (PBI-05204) inhibits the Na ⁺, K ⁺-ATPase activity with an IC₅₀ of 620 nM.

Istaroxime PST2744	Na+/K+ ATPase	Cardiovascular Disease
Istaroxime (PST2744) is a potent inhibitor of Na ⁺,K ⁺-ATPase with IC₅₀ of 0.11 μM.

Marinobufogenin	Na+/K+ ATPase	Cardiovascular Disease Neurological Disease Metabolic Disease
Marinobufogenin is a strong inhibitor of Na ⁺/K ⁺ ATPase that has been identified in mammalian plasma .

Sodium oleate 15+ Cited Publications Oleic acid sodium; 9-cis-Octadecenoic acid sodium; 9Z-Octadecenoic acid sodium	Na+/K+ ATPase Apoptosis	Metabolic Disease Cancer
Sodium oleate (Oleic acid sodium) is an abundant monounsaturated fatty acid sodium . Sodium oleate is a Na ⁺/K ⁺ ATPase activator .

Rimeporide hydrochloride EMD-87580 hydrochloride	Na+/H+ Exchanger (NHE)	Metabolic Disease
Rimeporide hydrochloride (EMD-87580 hydrochloride) is a potent and selective inhibitor of the Na ⁺/H ⁺ exchanger (NHE-1).

Prilocaine 1 Publications Verification	Na+/K+ ATPase	Neurological Disease
Prilocaine, an amino amide, is a Na, K-ATPase inhibitor. Prilocaine has neurotoxic effects .

Cat. No.	Product Name

HY-L118

Sodium Channel Blocker Library

128 compounds

Sodium channels conduct sodium ions (Na+) through a cell's plasma membrane that are the source of excitatory currents for the nervous system and muscle. Na channels are classified according to the trigger that opens the channel for such ions, i.e. either a voltage-change (Voltage-gated, voltage-sensitive, or voltage-dependent sodium channel also called VGSCs or Nav channel) or a binding of a substance (a ligand) to the channel (ligand-gated sodium channels). Dysfunction in voltage-gated sodium channels correlates with neurological and cardiac diseases, including epilepsy, myopathies, pain and cardiac arrhythmias. Sodium channel blockers are used in the treatment of cardiac arrhythmia, pain and convulsion.

MCE offers a unique collection of 128 sodium channel blocker and antagonists, all of which have the identified inhibitory effect on sodium channels. MCE Sodium Channel Blocker Library can be used for neurological and cardiac diseases drug discovery and sodium channel research.

HY-L166

Ion Channel Compound Library

1118 compounds

Ion channel is a membrane-binding enzyme whose catalytic site is an ion conduction pore, which is opened and closed in response to specific environmental stimuli (voltage, ligand concentration, membrane tension, temperature, etc.). Ion channel provide pores for the passive diffusion of ions on the biofilm. Due to their high selectivity for ion, ion channel are generally classified as sodium (Na⁺ ), potassium (K⁺ ), calcium (Ca²⁺ ), chloride (Cl^- ), and non-specific cation channel. Ion channel is an important contributor to cell signal transduction and homeostasis. In addition to electrical signal transduction, ion channel also have many functions: regulating vascular smooth muscle contraction, maintaining normal cell volume, regulating glandular secretion, protein kinase activation, etc. Therefore, dysfunction of ion channel can lead to many diseases, and its mechanism research is particularly important.

MCE designs a unique collection of 1118 small molecules related to ion channel, mainly targeting Na⁺ channel, K⁺ channel, Ca²⁺ channel, GABA receptor, iGluR, etc. It is an essential tool for research of cardiovascular diseases, Nervous system diseases and other diseases.

Cat. No.	Product Name	Type

HY-D1435

Oxonol VI	Fluorescent Dyes/Probes
Oxonol VI acts as an optical indicator for membrane potentials in lipid vesicles. Oxonol VI is suitable for detecting changes of membrane potential associated with the activity of the (Na ⁺ + K ⁺)-ATPase in reconstituted vesicles .

HY-D0085

DiSC3(5)

Fluorescent Dyes/Probes

DiSC3(5) is a fluorescent probe commonly used as a tracer dye to evaluate mitochondrial membrane potential. The excitation/emission wavelength of DiSC3(5) is up to 622/670 nm. DiSC3(5) can inhibit the respiratory system associated with mitochondrial NAD, and the IC₅₀ value is 8 μM. DiSC3(5) in the presence of Na ⁺/K ⁺-ATPase inhibitor ouabain 2 can induce membrane hyperpolarization of Ehrlich ascites tumor cells .

HY-126831

SBFI-AM

Fluorescent Dyes/Probes

SBFI-AM is a Na ⁺ selective fluorescent indicator. SBFI-AM shows selectivity for Na ⁺ over K ⁺ .

HY-D1760

SBFI Sodium-binding benzofuran isophthalate	Fluorescent Dyes/Probes
SBFI is a membrane-permeant, fluorescent Na ⁺ indicator dye. SBFI is excited at 340 nm and the fluorophore emission is collected at 450 nm . SBFI selective for Na ⁺ over K ⁺ with K_d values of 20 and 120 mM for these ions, respectively. .

HY-D0152

Tetramethylrhodamine-6-maleimide	Fluorescent Dyes/Probes
Tetramethylrhodamine-6-maleimide is a fluorescent dye with a reactive sulfhydryl-specific moiety is covalently coupled to this cysteine. Tetramethylrhodamine-6-maleimide can be used as labels to detect local protein motions of the fully active Na+/K+-ATPase in real time .

Cat. No.	Product Name	Type

HY-Y1889A

Sodium carboxymethyl cellulose (MW 250000) 5+ Cited Publications CMC-Na (MW 250000); CMC-Na (Viscosity:1500-3100 mPa.s)	Co-solvents
Sodium carboxymethyl cellulose (CMC-Na) (MW 250000) is a sodium salt of carboxymethyl cellulose. Sodium carboxymethyl cellulose has adsorption and corrosion inhibition on low-carbon steel in an acidic medium. Sodium carboxymethyl cellulose can be used as a thickener, paste and barrier agent .

HY-107754

Cesium chloride	Biochemical Assay Reagents
Cesium chloride is a blocker of potassium channel. Cesium chloride prevents the decrease of Na ⁺ transport produced by Alloxan . Cesium chloride has induced cardiac arrhythmias, including torsade de pointes in animal models .

HY-141613

1,2-Dioleoyl-sn-glycero-3-phospho-L-serine sodium DOPS-Na	Drug Delivery
1,2-Dioleoyl-sn-glycero-3-phospho-L-serine sodium is a ubstitute for Phosphoserine/phosphatidylserine. 1,2-Dioleoyl-sn-glycero-3-phospho-L-serine sodium can be used in lipid mixtures with DOPC and DOPE as effective nontoxic and nonviral DNA vectors .

HY-Y1889

Sodium carboxymethyl cellulose (Viscosity:5000-15000 mPa.s) CMC-Na (Viscosity:5000-15000 mPa.s)	Co-solvents
Sodium carboxymethyl cellulose (Viscosity:5000-15000 mPa.s) is the sodium salt of cellulose arboxymethyl and frequently used as viscous agent, paste and barrier agent.

HY-W040263

TAPS sodium TAPS Na	Buffer Reagents
TAPS sodium is a biological buffer that protects the structural integrity of lysozyme bacteria and prevents them from thermal denaturation at high temperatures. A pKa of 8.1 for TAPS results in half-maximal connexin channel activity .

HY-Y0703A

Sodium carboxymethyl cellulose (Viscosity:1200-1400 mPa.s) CMC-Na (Viscosity:1200-1400 mPa.s)	Biochemical Assay Reagents
Sodium carboxymethyl cellulose (Viscosity:1200-1400 mPa.s) is the sodium salt of cellulose arboxymethyl and frequently used as viscous agent, paste and barrier agent.

HY-Y0703C

Sodium carboxymethyl cellulose (Viscosity:300-800mpa.s) CMC-Na (Viscosity:300-800mpa.s)	Biochemical Assay Reagents
Sodium carboxymethyl cellulose (Viscosity:300-800mpa.s) is the sodium salt of cellulose arboxymethyl and frequently used as viscous agent, paste and barrier agent.

HY-P2837

Oxaloacetate decarboxylase	Biochemical Assay Reagents
Oxaloacetate decarboxylase catalyzes the irreversible decarboxylation of oxaloacetate to pyruvate and COIC₂. Oxaloacetate decarboxylase is a member of the sodium ion transport decarboxylase (NaT-DC) enzyme family. Oxaloacetate decarboxylase converts the chemical energy of the decarboxylation reaction into an electrochemical gradient of Na ⁺ ions across the membrane .

HY-157914

Dibenzyl-14-crown-4 6,6-Dibenzyl-1,4,8,11-tetraoxacyclotetradecane	Chelators
Dibenzyl-14-crown-4 (6,6-Dibenzyl-1,4,8,11-tetraoxacyclotetradecane) is a crown ether derivate, which serves as neutral carrier in PVC ion-selective electrode, improves the Li ⁺ selectivity against Na ⁺ and K ⁺ .

HY-D0157

ZnAF-2 ZNaF2; ZNaF 2; 4-[(2-{Bis[(pyridin-2-YL)methyl]amino}ethyl)amino]-2-(6-hydroxy-3-oxo-3H-xanthen-9-YL)benzoic acid	Biochemical Assay Reagents
ZnAF-2, 6-iso- is a cell-impermeable compound that acts as a high-affinity Zn2 -specific fluorescent probe (Kd = 2.7 nM). It exhibits low basal fluorescence with an approximately 51-fold increase in fluorescence intensity upon stoichiometric (1:1) binding to Zn2 . Little affinity for Ca2 , Mg2 , Na or K .

HY-Y0703D

Sodium carboxymethyl cellulose (average Mw 90000) CMC-Na (average Mw 90000, DS=0.7, Viscosity:50-200 mPa.s)	Biochemical Assay Reagents
Sodium carboxymethyl cellulose (average Mw 90000, DS=0.7, Viscosity:50-200 mPa.s) is the sodium salt of cellulose arboxymethyl and frequently used as viscous agent, paste and barrier agent .

HY-106150

Eniporide

EMD-96785

Biochemical Assay Reagents

Eniporide (EMD 96785) is a Na(+)/H(+) exchange (NHE) inhibitor. Eniporide specifically inhibits the NHE-1 isoform. Eniporide improves cardiac performance inhibition associated with myocardial ischemia/reperfusion in animals, and limits infarct size in experimental models. Eniporide regulates cardiac performance and high-energy phosphate content in clinically relevant pig models of CPB and cardiac arrest .

Cat. No.	Product Name	Target	Research Area

HY-P0117

Tat-NR2B9c Maximum Cited Publications 7 Publications Verification Tat-NR2Bct; Na-1	iGluR NO Synthase	Neurological Disease
Tat-NR2B9c (Tat-NR2Bct; NA-1) is a postsynaptic density-95 (PSD-95) inhibitor, with EC₅₀ values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B binding to PSD-95 with IC₅₀ values of 0.5 μM and 8 μM, respectively. Tat-NR2B9c also inhibits neuronal nitric oxide synthase (nNOS)/PSD-95 interaction, and possesses neuroprotective efficacy .

HY-P0117A

Tat-NR2B9c TFA Maximum Cited Publications 7 Publications Verification Tat-NR2Bct TFA; Na-1 TFA	iGluR NO Synthase	Neurological Disease
Tat-NR2B9c TFA (Tat-NR2Bct TFA) is a postsynaptic density-95 (PSD-95) inhibitor, with EC₅₀ values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c TFA disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B binding to PSD-95 with IC₅₀ values of 0.5 μM and 8 μM, respectively. Tat-NR2B9c TFA also inhibits neuronal nitric oxide synthase (nNOS)/PSD-95 interaction, and possesses neuroprotective efficacy .

HY-P1347A

RETF-4NA TFA

Peptides Metabolic Disease

RETF-4NA TFA, a chymase-specific substrate, is a sensitive and selective substrate for chymase when free or bound to α₂M .
HY-P1347

RETF-4NA

Peptides Metabolic Disease

RETF-4NA, a chymase-specific substrate, is a sensitive and selective substrate for chymase when free or bound to α₂M .

HY-P1920

CEF19, Epstein-Barr Virus latent NA-3A (458-466)	EBV	Inflammation/Immunology
CEF19, Epstein-Barr Virus latent NA-3A (458-466) is a single peptide epitope, YPLHEQHGM, representing residues 458-466 of the type 1 Epstein-Barr Virus (EBV) nuclear antigen 3A protein (B95.8 strain). CEF19, Epstein-Barr Virus latent NA-3A (458-466) can significantly affect cytotoxic T-lymphocyte (CTL) recognition .

HY-P2660

Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide

GD4K-Na
Enteropeptidase Others

Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide (GD4K-na) is a substrate for human enteropeptidase (K_m: 0.16 mM) .

HY-P1939

Cyclo(L-Leu-L-Pro) Cyclo(L-prolyl-L-leucyl)	Fungal	Infection
Cyclo(L-Leu-L-Pro) is an inhibitory substance targeting to production of norsolorinic acid (NA，a precursor of aflatoxin)，which can be isolated from A. xylosoxidans NFRI-A1. Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC₅₀ of 0.2 mg/mL in A. parasiticus SYS-4 .

HY-P1604

ATX-II	Sodium Channel	Inflammation/Immunology
ATX-II is a specific Na ⁺ channel Modulator toxin that can be isolated from the venom of sea anemone (Anemonia sulcata). ATX-II causes delayed inactivation of the Na ⁺

HY-P1604A

ATX-II TFA	Sodium Channel	Inflammation/Immunology
ATX-II TFA is a specific Na ⁺ channel Modulator toxin that can be isolated from the venom of sea anemone (Anemonia sulcata). ATX-II TFA causes delayed inactivation of the Na ⁺

HY-P3278

Caloxin 2A1	Proton Pump	Metabolic Disease
Caloxin 2A1 is an extracellular plasma membrane Ca ²⁺-ATPase (PMCA) peptide inhibitor. Caloxin 2A1 does not affect basal Mg ²⁺-ATPase or Na ⁺-K ⁺-ATPase .

HY-P3278A

Caloxin 2A1 TFA 1 Publications Verification	Proton Pump	Metabolic Disease
Caloxin 2A1 TFA is an extracellular plasma membrane Ca ²⁺-ATPase (PMCA) peptide inhibitor. Caloxin 2A1 TFA does not affect basal Mg ²⁺-ATPase or Na ⁺-K ⁺-ATPase .

HY-P5816

BmK-M1	Sodium Channel	Neurological Disease
BmK-M1 is a scorpion toxin, and is composed of 64 amino acids cross-linked by four disulfide bridges. BmK-M1 inhibits Na ⁺ channel and can be considered both as a cardiotoxin and a neurotoxin .

HY-P3711

SPAI-1	Na+/K+ ATPase	Others
SPAI-1 is a specific inhibitor for monovalent cation transporting ATPases. SPAI-1 is a peptide isolated from porcine duodenum, inhibits Na ⁺, K ⁺-ATPase and H ⁺, K ⁺-ATPase in vitro, stimulates Mg ²⁺-ATPase .

HY-P2837

Oxaloacetate decarboxylase	Endogenous Metabolite	Metabolic Disease
Oxaloacetate decarboxylase catalyzes the irreversible decarboxylation of oxaloacetate to pyruvate and COIC₂. Oxaloacetate decarboxylase is a member of the sodium ion transport decarboxylase (NaT-DC) enzyme family. Oxaloacetate decarboxylase converts the chemical energy of the decarboxylation reaction into an electrochemical gradient of Na ⁺ ions across the membrane .

HY-P5159

Crotamine	Sodium Channel	Inflammation/Immunology
Crotamine is a Na ⁺ channel modulator. Crotamine is a 42 amino acid toxin cross-linked by three disulfide bridges. Crotamine has analgesic activity. Crotamine also interacts with lipid membranes and shows myonecrotic activity. Crotamine can be isolated from Crotalus durissus terrificus venom .

HY-P1833

Egg Laying Hormone, aplysia	Peptides	Neurological Disease
Egg Laying Hormone, aplysia is a neuropeptide synthesized by the bag cell neurons, which contains 36 amino acids and can stimulate egglaying and ovulation in Aplysia via electrical discharge triggering of neurons. Egg-laying hormone of Aplysia induces a voltage-dependent slow inward current carried by Na' in an identified motoneuron .

HY-P1531

γ-1-Melanocyte Stimulating Hormone (MSH), amide	Melanocortin Receptor	Metabolic Disease Endocrinology
γ-1-Melanocyte Stimulating Hormone (MSH), amide is a 11-amino acid peptide. γ-1-Melanocyte Stimulating Hormone (MSH) regulates sodium (Na ⁺) balance and blood pressure through activation of the melanocortin receptor 3 (MC3-R).

HY-P1565A

Transdermal Peptide Disulfide TFA TD 1 Disulfide(peptide) TFA	Na+/K+ ATPase	Others
Transdermal Peptide Disulfide TFA (TD 1 Disulfide(peptide) TFA) is a 11-amino acid peptide, binds to Na ⁺/K ⁺-ATPase beta-subunit (ATP1B1), and mainly interacts with the C-terminus of ATP1B1. Transdermal Peptide Disulfide TFA can enhance the transdermal delivery of many macromolecules .

HY-P1769

Angiotensin II (5-8), human	Angiotensin Receptor	Metabolic Disease Endocrinology
Angiotensin II (5-8), human is an endogenous C-terminal fragment of the peptide vasoconstrictor angiotensin II . Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca ²⁺ levels. Angiotensin II also acts at the Na ⁺/H ⁺ exchanger in the proximal tubules of the kidney .

HY-P1792

Angiotensin II (1-4), human	Angiotensin Receptor	Metabolic Disease Endocrinology
Angiotensin II (1-4), human is an endogenous peptide produced from AT I by angiotensin-converting-enzyme (ACE). Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca ²⁺ levels. Angiotensin II also acts at the Na ⁺/H ⁺ exchanger in the proximal tubules of the kidney .

HY-P1792A

Angiotensin II (1-4), human TFA	Angiotensin Receptor	Metabolic Disease Endocrinology
Angiotensin II (1-4), human (TFA) is an endogenous peptide produced from AT I by angiotensin-converting-enzyme (ACE). Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca ²⁺ levels. Angiotensin II also acts at the Na ⁺/H ⁺ exchanger in the proximal tubules of the kidney .

HY-P1073

ProTx-I	Calcium Channel Sodium Channel Potassium Channel	Cancer
ProTx-I, a venom toxin of the tarantula Thrixopelma pruriens, is a potent, selective Ca_V3.1 channel blocker with IC₅₀ values of 0.2 μM and 31.8 μM for hCa_V3.1 and hCa_V3.2 respectively. ProTx-I is also a potent blocker for voltage-gated Na ⁺ channels and inhibits K_V 2.1 channels .

HY-P10228

S-Thanatin	Fungal Bacterial	Infection
S-Thanatin is an insect antimicrobial peptide with potent broad-spectrum antibacterial activity. S-Thanatin can inhibit the activity of Gram-negative bacteria, Gram-positive bacteria, and fungi, without cytotoxicity. The antibacterial activity of S-Thanatin is not affected by PH value, but monovalent cations (Na ⁺/K ⁺) can reduce its antibacterial activity against Gram-negative bacteria in a dose-dependent manner .

HY-P5869

Kurtoxin	Calcium Channel Sodium Channel	Neurological Disease
Kurtoxin is a selective Cav3 (T-type) voltage-gated Ca ²⁺ channel gating inhibitor with a K_d of 15 nM for Cav3.1 (α1G T-type) Ca ²⁺ channel. Kurtoxin can interact with high affinity with native neuronal high-threshold L-type, N-type, and P-type Ca ²⁺ channels in central and peripheral neurons. Kurtoxin also shows cross-reactivity with voltage-gated Na ⁺ channel .

HY-P5876

Proadrenomedullin (N-20) (bovine, porcine) ProADM N20(bovine, porcine); PAMP-20(bovine, porcine)	nAChR	Neurological Disease
Proadrenomedullin (N-20) (ProADM N20) (bovine, porcine) is a potent and noncompetitive hypotensive and catecholamine release-inhibitory peptide released from chromaffin cells. Proadrenomedullin (N-20) (bovine, porcine) inhibits catecholamine secretion with an IC₅₀ of 350 nM in PC12 pheochromocytoma cells. Proadrenomedullin (N-20) (bovine, porcine) also blocks (EC₅₀≈270 nM) nicotinic cholinergic agonist desensitization of catecholamine release, as well as desensitization of nicotinic signal transduction ( ²²Na ⁺ uptake) .

Cat. No.	Product Name

HY-K1015

TAE Powder (1 L of 1×)

MCE TAE Powder (1 L of 1×) consists of Tris-acetate and EDTA-2Na, and is widely used in agarose gel electrophoresis of nucleic acid.

Species:	Human (14) Virus (70)
Tag:	His (66) Tag Free (17) Strep (1) Avi (3) GST (1) MBP (1) Fc (1) Flag (2)
Source:	HEK293 (68) E. coli Cell-free (1) CHO (1) Sf9 insect cells (14)

Cat. No.	Compare	Product Name	Species	Source

HY-P70393

	*HLA-A0201 HPV16 E7 complex Protein, Human (HEK293, His)** rHuHLA-A*0201 HPV16 E7 complex Protein, His; Na	Human	HEK293
	B2M is a component of MHC class I complexes that present peptide antigens to the immune system. HLA-A0201 HPV16 E7 complex Protein, Human (HEK293, His) is a recombinant protein dimer complex containing human-derived HLA-A0201 HPV16 E7 complex protein, expressed by HEK293 , with C-10His labeled tag. HLA-A0201 HPV16 E7 complex Protein, Human (HEK293, His), has molecular weight of 55-60 kDa.

HY-P70391

	*HLA-A0201 AFP complex Protein, Human (HEK293, His)** rHuHLA-A*0201 AFP complex Protein, His; Na	Human	HEK293
	B2M is a component of MHC class I complexes that present peptide antigens to the immune system. HLA-A0201 AFP complex Protein, Human (HEK293, His) is a recombinant protein dimer complex containing human-derived HLA-A0201 AFP complex protein, expressed by HEK293 , with C-10His labeled tag. HLA-A0201 AFP complex Protein, Human (HEK293, His), has molecular weight of 55-60 kDa.

HY-P70392

	*HLA-A0201 GP100 complex Protein, Human (A269V, HEK293, His)** rHuHLA-A*0201 GP100 complex Protein, His; Na	Human	HEK293
	B2M is a component of MHC class I complexes that present peptide antigens to the immune system. HLA-A0201 GP100 complex Protein, Human (A269V, HEK293, His) is a recombinant protein dimer complex containing human-derived HLA-A0201 GP100 complex protein, expressed by HEK293 , with C-10His labeled tag. HLA-A0201 GP100 complex Protein, Human (A269V, HEK293, His), has molecular weight of 55-60 kDa.

HY-P70395

HLA-A*0201 WT-1 complex Protein, Human (HEK293, His)

rHuHLA-A*0201 WT-1 complex Protein, His; Na
Human HEK293

HY-P73231

	NA/Neuraminidase Protein, Influenza A H1N1 (HEK293) Na; Neuraminidase	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, Influenza A H1N1 (HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, Influenza A H1N1 (HEK293) is 434 a.a., with molecular weight of ~47.8 kDa.

HY-P73233

	NA/Neuraminidase Protein, Influenza A H3N2 (HEK293) Na; Neuraminidase	Virus	HEK293
	Neuraminidase proteins catalyze the removal of terminal sialic acid residues from viral and cellular glycoconjugates, facilitating virus release and spread. NA/Neuraminidase Protein, Influenza A H3N2 (HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, Influenza A H3N2 (HEK293) is 469 a.a., with molecular weight of ~52.2 kDa.

HY-P73771

	NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (HEK293)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293) is 424 a.a., .

HY-P73755

	NA/Neuraminidase Protein, Influenza B (AAA43749, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, Influenza B (B/Lee/1940, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, Influenza B (AAA43749, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, Influenza B (AAA43749, HEK293, His) is 435 a.a., with molecular weight of ~50.6 kDa.

HY-P73756

NA/Neuraminidase Protein, Influenza B (4CPL_A, HEK293)

Na; Neuraminidase; Na/Neuraminidase Protein, Influenza B (B/Brisbane/60/2008, HEK293)
Virus HEK293

HY-P73754

	NA/Neuraminidase Protein, Influenza B (EPI529344, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, Influenza B (B/PHUKET/3073/2013, sf9, His)	Virus	Sf9 insect cells
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, Influenza B (EPI529344, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with N-His labeled tag. The total length of NA/Neuraminidase Protein, Influenza B (EPI529344, sf9, His) is 429 a.a., with molecular weight of ~49.5 kDa.

HY-P73777

	NA/Neuraminidase Protein, H1N1 (P03469, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/USSR/90/1977, HEK293)	Virus	HEK293
	NA/Neuraminidase Protein, an enzyme found on the surface of influenza viruses, is responsible for the cleavage of sialic acid residues. Inhibition of NA/Neuraminidase Protein is a key target for antiviral drugs. Targeting NA/Neuraminidase Protein may provide potential therapeutic interventions by preventing viral release, reducing viral spread, and potentially treating influenza infections. NA/Neuraminidase Protein, H1N1 (P03469, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H1N1 (P03469, HEK293) is 470 a.a., with molecular weight of ~51.9 kDa.

HY-P73236

	NA/Neuraminidase Protein, Influenza A H3N2 (N294S, HEK293) Na; Neuraminidase	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, Influenza A H3N2 (N294S, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. and N294S mutation. The total length of NA/Neuraminidase Protein, Influenza A H3N2 (N294S, HEK293) is 424 a.a., .

HY-P73237

	NA/Neuraminidase Protein, Influenza A H3N2 (R292K, HEK293) Na; Neuraminidase	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, Influenza A H3N2 (R292K, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. and R292K mutation. The total length of NA/Neuraminidase Protein, Influenza A H3N2 (R292K, HEK293) is 424 a.a., .

HY-P73239

	NA/Neuraminidase Protein, Influenza A H5N1 (H255Y, HEK293) Na; Neuraminidase	Virus	HEK293
	Neuraminidase (NA) is described as a receptor-destroying enzyme because it cleaves a terminal sialic acid from the cellular receptors. Whereby, NA facilitates viral invasion of the upper airways, facilitates virus release during virus budding, prevents self-aggregation and ensures the efficient spread of the progeny virus from cell to cell, and also plays a role in the determination of host range restriction on replication and virulence. NA/Neuraminidase Protein, Influenza A H5N1 (H255Y, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. and H255Y mutation. The total length of NA/Neuraminidase Protein, Influenza A H5N1 (H255Y, HEK293) is 449 a.a., with molecular weight of ~49.2 kDa.

HY-P73778

	NA/Neuraminidase Protein, H1N1 (P03468, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Puerto Rico/8/1934, HEK293)	Virus	HEK293
	The NA/Neuraminidase Protein is an influenza virus surface enzyme that cleaves sialic acid residues. Inhibiting NA/Neuraminidase Protein is crucial for antiviral drugs. Targeting NA/Neuraminidase Protein can help prevent viral release, reduce viral spread, and potentially treat influenza infections. NA/Neuraminidase Protein, H1N1 (P03468, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H1N1 (P03468, HEK293) is 454 a.a., with molecular weight of ~50.1 kDa.

HY-P73796

	NA/Neuraminidase Protein, H1N1 (ABO38354, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Henry/1936, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ABO38354, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ABO38354, HEK293, His) is 434 a.a., with molecular weight of ~50.3 kDa.

HY-P73757

	NA/Neuraminidase Protein, H5N1 (AEO89183, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H5N1 (A/Hubei/1/2010, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H5N1 (AEO89183, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H5N1 (AEO89183, HEK293, His) is 413 a.a., with molecular weight of ~52 kDa.

HY-P73758

	NA/Neuraminidase Protein, H5N1 (ABU94738, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H5N1 (A/Anhui/1/2005, sf9, His)	Virus	Sf9 insect cells
	Neuraminidase (NA) is described as a receptor-destroying enzyme because it cleaves a terminal sialic acid from the cellular receptors. Whereby, NA facilitates viral invasion of the upper airways, facilitates virus release during virus budding, prevents self-aggregation and ensures the efficient spread of the progeny virus from cell to cell, and also plays a role in the determination of host range restriction on replication and virulence. NA/Neuraminidase Protein, H5N1 (ABU94738, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H5N1 (ABU94738, sf9, His) is 414 a.a., with molecular weight of ~51.1 kDa.

HY-P73761

	NA/Neuraminidase Protein, H3N2 (H274Y, ACN50232, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (H274Y, HEK293)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (H274Y, ACN50232, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H3N2 (H274Y, ACN50232, HEK293) is 424 a.a., .

HY-P73764

	NA/Neuraminidase Protein, H3N2 (E119V, ACN50232, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (E119V, HEK293)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (E119V, ACN50232, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H3N2 (E119V, ACN50232, HEK293) is 424 a.a., .

HY-P73765

	NA/Neuraminidase Protein, H3N2 (AVG71505, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Kansas/14/2017, sf9, His)	Virus	Sf9 insect cells
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (AVG71505, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (AVG71505, sf9, His) is 440 a.a., with molecular weight of ~56.5 kDa.

HY-P73766

	NA/Neuraminidase Protein, H3N2 (AFG72176, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Amsterdam/4112/1992, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (AFG72176, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (AFG72176, HEK293, His) is 434 a.a., with molecular weight of ~50.8 kDa.

HY-P73770

	NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Babol/36/2005, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (ACN50232, HEK293, His) is 424 a.a., with molecular weight of ~80 kDa.

HY-P73773

	NA/Neuraminidase Protein, H3N2 (ABO44071, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Albany/18/1968, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H3N2 (ABO44071, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (ABO44071, HEK293, His) is 434 a.a., with molecular weight of ~50.8 kDa.

HY-P73776

	NA/Neuraminidase Protein, H1N1 (P03469, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/USSR/90/1977, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein, an enzyme found on the surface of influenza viruses, is responsible for the cleavage of sialic acid residues. Inhibition of NA/Neuraminidase Protein is a key target for antiviral drugs. Targeting NA/Neuraminidase Protein may provide potential therapeutic interventions by preventing viral release, reducing viral spread, and potentially treating influenza infections. NA/Neuraminidase Protein, H1N1 (P03469, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (P03469, HEK293, His) is 435 a.a., with molecular weight of ~76.6 kDa.

HY-P73780

	NA/Neuraminidase Protein, H1N1 (H275Y, ACP41107, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (H275Y, HEK293)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (H275Y, ACP41107, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H1N1 (H275Y, ACP41107, HEK293) is 434 a.a., with molecular weight of ~47.8 kDa.

HY-P73781

	NA/Neuraminidase Protein, H1N1 (EPI859652, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Michigan/45/2015, sf9, His)	Virus	Sf9 insect cells
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (EPI859652, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (EPI859652, sf9, His) is 434 a.a., with molecular weight of ~53.6 kDa.

HY-P73782

	NA/Neuraminidase Protein, H1N1 (EPI859651, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Michigan/45/2015, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (EPI859651, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (EPI859651, HEK293, His) is 434 a.a., with molecular weight of ~50.2 kDa.

HY-P73783

	NA/Neuraminidase Protein, H1N1 (EPI1799927, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Brisbane/02/2018, sf9, His)	Virus	Sf9 insect cells
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (EPI1799927, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (EPI1799927, sf9, His) is 440 a.a., with molecular weight of ~62.6 kDa.

HY-P73786

	NA/Neuraminidase Protein, H1N1 (AQS19400, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Idaho/01/2017, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (AQS19400, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (AQS19400, HEK293, His) is 434 a.a., with molecular weight of ~50.2 kDa.

HY-P73790

	NA/Neuraminidase Protein, H1N1 (ACP41107, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/California/04/2009, sf9, His)	Virus	Sf9 insect cells
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ACP41107, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ACP41107, sf9, His) is 434 a.a., with molecular weight of ~58.7 kDa.

HY-P73791

	NA/Neuraminidase Protein, H1N1 (ACP41107, HEK293, Fc) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/California/04/2009, HEK293, Fc)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ACP41107, HEK293, Fc) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-hFc labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ACP41107, HEK293, Fc) is 434 a.a., with molecular weight of 95-105 kDa.

HY-P73792

	NA/Neuraminidase Protein, H1N1 (ACM51249, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/ArizoNa/13/2008, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (ACM51249, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ACM51249, HEK293, His) is 435 a.a., with molecular weight of ~50.3 kDa.

HY-P73793

	NA/Neuraminidase Protein, H1N1 (ACF41870, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Beijing/262/1995, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ACF41870, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ACF41870, HEK293, His) is 435 a.a., with molecular weight of ~50.3 kDa.

HY-P73794

	NA/Neuraminidase Protein, H1N1 (ABR28848, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Auckland/606/2001, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ABR28848, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ABR28848, HEK293, His) is 435 a.a., with molecular weight of ~50.2 kDa.

HY-P73795

	NA/Neuraminidase Protein, H1N1 (ABQ53689, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Auckland/6/1996, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ABQ53689, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ABQ53689, HEK293, His) is 435 a.a., with molecular weight of ~50.5 kDa.

HY-P73797

	NA/Neuraminidase Protein, H1N1 (ABO38057, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/AA/Marton/1943, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ABO38057, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ABO38057, HEK293, His) is 434 a.a., with molecular weight of ~50.1 kDa.

HY-P73798

	NA/Neuraminidase Protein, H1N1 (ABD95342, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/Baylor/11515/1982, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (ABD95342, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (ABD95342, HEK293, His) is 435 a.a., with molecular weight of ~50.4 kDa.

HY-P73762

	NA/Neuraminidase Protein, H3N2 (EPI675797, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Hong Kong/4801/2014, sf9, His)	Virus	Sf9 insect cells
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (EPI675797, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells , with C-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (EPI675797, sf9, His) is 434 a.a., with molecular weight of ~53.9 kDa.

HY-P73763

	NA/Neuraminidase Protein, H3N2 (EPI675797, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Hong Kong/4801/2014, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (EPI675797, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (EPI675797, HEK293, His) is 434 a.a., with molecular weight of ~50.5 kDa.

HY-P73767

	NA/Neuraminidase Protein, H3N2 (AFG71945, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Hong Kong/107/1971, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (AFG71945, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (AFG71945, HEK293, His) is 434 a.a., with molecular weight of ~50.6 kDa.

HY-P73768

	NA/Neuraminidase Protein, H3N2 (AEG65596, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Australia/NHRC0001/2005, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (AEG65596, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (AEG65596, HEK293, His) is 434 a.a., with molecular weight of ~50.6 kDa.

HY-P73769

	NA/Neuraminidase Protein, H3N2 (ADT79152, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/swine/Italy/526/1985, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (ADT79152, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (ADT79152, HEK293, His) is 434 a.a., with molecular weight of ~50.7 kDa.

HY-P73774

	NA/Neuraminidase Protein, H1N1 (QEM24782, sf9, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/swine/Shandong/1207/2016, sf9, His)	Virus	Sf9 insect cells
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (QEM24782, sf9, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by Sf9 insect cells, with C-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (QEM24782, sf9, His) is 440 a.a., with molecular weight of ~54.6 kDa.

HY-P73779

	NA/Neuraminidase Protein, H1N1 (N295S, ACP41107, HEK293) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (N295S , HEK293)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (N295S, ACP41107, HEK293) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with tag free. The total length of NA/Neuraminidase Protein, H1N1 (N295S, ACP41107, HEK293) is 469 a.a., with molecular weight of ~52 kDa.

HY-P73787

	NA/Neuraminidase Protein, H1N1 (AKM14549, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/swine/CaNada/01093/2006, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H1N1 (AKM14549, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (AKM14549, HEK293, His) is 434 a.a., with molecular weight of ~50.2 kDa.

HY-P73799

	NA/Neuraminidase Protein, H1N1 (AAF77044, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H1N1 (A/swine/Iowa/15/1930, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H1N1 (AAF77044, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H1N1 (AAF77044, HEK293, His) is 434 a.a., with molecular weight of ~50.3 kDa.

HY-P73759

	NA/Neuraminidase Protein, H3N2 (QGZ99158, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/swine/ChiNa/JG20/2019, HEK293, His)	Virus	HEK293
	NA/Neuraminidase Protein is a receptor-destroying enzyme that cleaves terminal sialic acids from cellular receptors, potentially facilitating viral invasion of the upper airways by targeting sialic acid moieties on airway epithelial cell mucin. NA plays a pivotal role in viral propagation by catalyzing the removal of terminal sialic acid residues from both viral and cellular glycoconjugates. Moreover, the sialidase activity in late endosome/lysosome traffic appears to enhance virus replication. NA/Neuraminidase Protein, H3N2 (QGZ99158, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293, with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (QGZ99158, HEK293, His) is 435 a.a., with molecular weight of ~50.6 kDa.

HY-P73760

	NA/Neuraminidase Protein, H3N2 (Q75VQ4, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Aichi/2/1968, HEK293, His)	Virus	HEK293
	Neuraminidase proteins catalyze the removal of terminal sialic acid residues from viral and cellular glycoconjugates, facilitating virus release and spread. NA/Neuraminidase Protein, H3N2 (Q75VQ4, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (Q75VQ4, HEK293, His) is 434 a.a., with molecular weight of ~76.8 kDa.

HY-P73772

	NA/Neuraminidase Protein, H3N2 (ACF36533, HEK293, His) Na; Neuraminidase; Na/Neuraminidase Protein, H3N2 (A/Hong Kong/CUHK19579/1998, HEK293, His)	Virus	HEK293
	NA (neuraminidase) proteins play a key role in viral transmission by catalyzing the removal of terminal sialic acid residues from viral and cellular glycoconjugates. NA plays a role in determining host range, limiting replication, and virulence. NA is associated with the development and progression of type 2 diabetes mellitus (T2D). NA/Neuraminidase Protein, H3N2 (ACF36533, HEK293, His) is the recombinant Virus-derived NA/Neuraminidase protein, expressed by HEK293 , with N-His labeled tag. The total length of NA/Neuraminidase Protein, H3N2 (ACF36533, HEK293, His) is 434 a.a., with molecular weight of ~50.4 kDa.

Cat. No.	Product Name	Chemical Structure

HY-B1039AS

Ambroxol-d5 hydrochloride

Ambroxol-d₅ (hydrochloride) is the deuterium labeled Ambroxol hydrochloride. Ambroxol hydrochloride (NA-872 hydrochloride), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol hydrochloride is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol hydrochloride induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research[1][2].

HY-B0575S

Triamterene-d5

Triamterene-d₅ is deuterium labeled Triamterene, which can block epithelial Na+ channel (ENaC) in a voltage-dependent manner, which used as a mild diuretic.

HY-Y0258S

Benzocaine-d4
Benzocaine-d₄ is the deuterium labeled Benzocaine. Benzocaine shares a common receptor with all othe rLAs in the voltage-gated Na+ channel, with an IC50 of 0.8 mM tested with a potential of +30 mV.

HY-N1446S5

Oleic acid-d9

Oleic acid-d₉ is deuterium labeled Oleic acid. Oleic acid is an abundant monounsaturated fatty acid. Oleic acid is a Na+/K+ ATPase activator[1][2].

HY-B0137AS

Prilocaine-d7 hydrochloride
Prilocaine-d₇ (hydrochloride) is deuterium labeled Prilocaine (hydrochloride). Prilocaine hydrochloride, an amino amide, is a Na, K-ATPase inhibitor. Prilocaine has neurotoxic effects[1][2].

HY-N1446S

Oleic acid-13C
Oleic acid- ¹³C is the ¹³C labeled Oleic acid. Oleic acid (9-cis-Octadecenoic acid) is an abundant monounsaturated fatty acid[1]. Oleic acid is a Na+/K+ ATPase activator[2].

HY-Y0258S1

Benzocaine-(ethyl-d5)
Benzocaine-(ethyl-d₅) is the deuterium labeled Benzocaine. Benzocaine shares a common receptor with all othe rLAs in the voltage-gated Na+ channel, with an IC50 of 0.8 mM tested with a potential of +30 mV.

HY-N1446S3

Oleic acid-d17
Oleic acid-d₁₇ is the deuterium labeled Oleic acid. Oleic acid (9-cis-Octadecenoic acid) is an abundant monounsaturated fatty acid[1]. Oleic acid is a Na+/K+ ATPase activator[2].

HY-N1446S2

Oleic acid-13C18
Oleic acid- ¹³C₁₈ is the ¹³C labeled Oleic acid. Oleic acid (9-cis-Octadecenoic acid) is an abundant monounsaturated fatty acid[1]. Oleic acid is a Na+/K+ ATPase activator[2].

HY-N1446S1

Oleic acid-d2
Oleic acid-d₂) is the deuterium labeled Oleic acid. Oleic acid (9-cis-Octadecenoic acid) is an abundant monounsaturated fatty acid[1]. Oleic acid is a Na+/K+ ATPase activator[2].

HY-N1446S4

Oleic acid-13C-1
Oleic acid- ¹³C-1 is the ¹³C labeled Oleic acid. Oleic acid (9-cis-Octadecenoic acid) is an abundant monounsaturated fatty acid[1]. Oleic acid is a Na+/K+ ATPase activator[2].

HY-B0448S

Phenytoin-d10
Phenytoin-d₁₀ is the deuterium labeled Phenytoin. Phenytoin (5,5-Diphenylhydantoin) is a potent Voltage-gated Na+ channels (VGSCs) blocker. Phenytoin has antiepileptic activity and reduces breast tumour growth and metastasis in mice[1][2].

HY-17468S

Bumetanide-d5
Bumetanide-d₅ is a deuterium labeled Bumetanide. Bumetanide is a selective Na+-K+-Cl- (NKCC1) inhibitor, weakly inhibits NKCC2, with IC50s of 0.68 and 4.0 μM for hNKCC1A and hNKCC2A, respectively[1].

HY-B0211S

Riluzole-13C,15N2
Riluzole- ¹³C, ¹⁵N₂ is the ¹³C and ¹⁵N labeled Riluzole[1]. Riluzole is an anticonvulsant agent and belongs to the family of use-dependent Na+ channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM[2][3].

HY-B0448S1

Phenytoin-15n2,13c
Phenytoin- ¹⁵N₂, ¹³C is the ¹³C and ¹⁵N labeled Phenytoin[1]. Phenytoin (5,5-Diphenylhydantoin) is a potent Voltage-gated Na+ channels (VGSCs) blocker. Phenytoin has antiepileptic activity and reduces breast tumour growth and metastasis in mice[2][3].

HY-B0495S4

Lamotrigine-13C3
Lamotrigine- ¹³C₃ is the ¹³C-labeled Lamotrigine. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al[1][2].

HY-B0495S5

Lamotrigine-d3
Lamotrigine-d3 is the deuterium labeled Lamotrigine[1]. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al[2][3].

HY-B0495S1

Lamotrigine-13C,d3
Lamotrigine- ¹³C,d₃ is the ¹³C- and deuterium labeled Lamotrigine. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al[1][2].

HY-B0495S

Lamotrigine-13C3,d3
Lamotrigine- ¹³C₃,d₃ is the ¹³C-labeled Lamotrigine. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al[1][2].

HY-B0495S3

Lamotrigine-13C2,15N
Lamotrigine-13C2,15N is the 13C and 15N labeled Lamotrigine[1]. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al[2][3].

HY-13295S

Vinpocetine-d5

Vinpocetine-d₅ is the deuterium labeled Vinpocetine. Vinpocetine (Ethyl apovincaminate) is a derivative of the alkaloid Vincamine that blocks voltage-gated Na+ channels. The IC50 value of Vinpocetine on direct IKK inhibition in the cell-free system is 17.17 μM. Vinpocetine is a phosphodiesterase (PDE) inhibitor and inhibits NF-κB-dependent inflammatory responses by directly targeting IκB kinase complex (IKK), and has been widely used for the treatment of cerebrovascular disorders[1][2][3].

HY-100490S

Rilmenidine-d4

Rilmenidine-d₄ is the deuterium labeled Rilmenidine. Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells[1][2][3].

HY-B0135S

Furosemide-d5

Furosemide-d₅ is the deuterium labeled Furosemide. Furosemide is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, NKCC1 and NKCC2[1]. Furosemide is also a GABAA receptors antagonist and displays 100-fold selectivity for α6-containing receptors than α1-containing receptors. Furosemide acts as a loop diuretic and used for the study of congestive heart failure, hypertension and edema[2].

Cat. No.	Product Name	Application	Reactivity

HY-P81122

NIS Antibody Na(+)/I(-) cotransporter; Na(+)/I(-) symporter; Na(+)/I(-) cotransporter; Na(+)/I(-) symporter; Na+/I- cotransporter; Na+/I-symporter; NIS; SC5A5_HUMAN; SLC5A5; sodium iodide symporter; Sodium-iodide symporter; Sodium/iodide cotransporter; Solute carrier family 5 (sodium iodide symporter) member 5; Solute carrier family 5; Solute carrier family 5 member 5.	WB; ELISA; IHC-P; IHC-F; IF	Mouse, Rat(predicted: Human)
NIS Antibody is an unconjugated, approximately 68 kDa, rabbit-derived, anti-NIS polyclonal antibody. NIS Antibody can be used for: WB, ELISA, IHC-P, IHC-F, IF expriments in mouse, rat, and predicted: human background without labeling.

HY-P80537

ATP1A1 Antibody A1A1; AT1A1; ATP1A1; Na+/K+ transporting; alpha 1 polypeptide; Na+/K+ ATPase 1; Na; K-ATPase 1; Sodium pump 1	WB, IHC-P, ICC/IF, FC	Human, Mouse, Rat
alpha 1 Sodium Potassium ATPase Antibody is a non-conjugated and Rabbit origined polyclonal antibody about 113 kDa, targeting to alpha 1 Sodium Potassium ATPase. It can be used for WB,IHC-P,ICC/IF,FC assays with tag free, in the background of Human, Mouse, Rat.

HY-P82586

NCX1 Antibody (YA2331)

Na+/Ca2+ exchanger; NCX1; SLC8A1
WB Human, Mouse, Rat

HY-P81857

Clusterin Antibody (YA1602) CLU; APOJ; CLI; KUB1; AAG4; Clusterin; Aging-associated gene 4 protein; Apolipoprotein J; Apo-J; Complement cytolysis inhibitor; CLI; Complement-associated protein SP-40; 40; Ku70-binding protein 1; Na1/Na2; Testosterone-repressed prostate m	WB, IHC-P	Human, Mouse

HY-P81437

SLC34A2 Antibody (YA1182) SLC34A2; Sodium-dependent phosphate transport protein 2B; Sodium-phosphate transport protein 2B; Na(+)-dependent phosphate cotransporter 2B; NaPi3b; Sodium/phosphate cotransporter 2B (Na(+)/Pi cotransporter 2B; NaPi-2b); Solute carrier family 34 member 2	IHC-P	Human

HY-P81204

Alpha-ENaC Antibody Alpha ENaC 2; Alpha ENaC; Alpha NaCH; Alpha-NaCH; Amiloride sensitive epithelial sodium channel alpha subunit; Amiloride sensitive sodium channel subunit alpha; Amiloride-sensitive sodium channel subunit alpha; ENaCa; ENaCalpha; Epithelial Na(+) channel subunit alpha; Epithelial Na+ channel subunit alpha; FLJ21883; Nonvoltage gated sodium channel 1 subunit alpha; Nonvoltage-gated sodium channel 1 subunit alpha; SCNEA; SCNN 1; SCNN1; SCNN1A; SCNNa_HUMAN; Sodium channel nonvoltage gated 1 alpha.	WB; ELISA; IHC-P; IHC-F; Flow-Cyt; IF	Human, Mouse, Rat(predicted: Dog, Pig, Cow, Horse, Sheep)
Alpha-ENaC Antibody is an unconjugated, approximately 76 kDa, rabbit-derived, anti-Alpha-ENaC polyclonal antibody. Alpha-ENaC Antibody can be used for: WB, ELISA, IHC-P, IHC-F, Flow-Cyt, IF expriments in human, mouse, rat, and predicted: dog, pig, cow, horse, sheep background without labeling.

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