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DT

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Adenosine Receptor (1) Antibody-Oligonucleotide Conjugates (AOCs) (1) Apoptosis (2) Bacterial (1) Bcl-2 Family (2) c-Fms (1) c-Kit (1) Caspase (2) Complement System (3) COX (1) Cyclic GMP-AMP Synthase (1) Dengue Virus (1) DNA/RNA Synthesis (34) Drug Derivative (2) Drug Intermediate (1) E3 Ligase Ligand-Linker Conjugates (1) Endogenous Metabolite (2) Environmental Pollutants (1) ERK (1) Flavivirus (1) Fluorescent Dye (1) Fungal (1) HCV (2) Herbicide (1) IFNAR (1) Integrin (1) Interleukin Related (4) Isotope-Labeled Compounds (4) JNK (1) Ligands for Target Protein for PROTAC (1) Liposome (3) Macrophage migration inhibitory factor (MIF) (2) MicroRNA (3) NO Synthase (1) NOD-like Receptor (NLR) (1) Nucleoside Antimetabolite/Analog (7) p38 MAPK (1) Parasite (1) PCSK9 (1) Phosphatase (3) Phosphoramidites (28) PKG (3) Poly(ADP-ribose) Glycohydrolase (PARG) (2) PPAR (1) Prostaglandin Receptor (2) PROTACs (2) Pyroptosis (1) Ras (1) Reactive Oxygen Species (ROS) (1) Reference Standards (1) Small Interfering RNA (siRNA) (7) STING (1) TGF-beta/Smad (1) Thyroid Hormone Receptor (1) TNF Receptor (1) Toll-like Receptor (TLR) (1) Transthyretin (TTR) (1) VEGFR (1)
By Research Areas:	Cancer (26) Cardiovascular Disease (9) Infection (7) Inflammation/Immunology (9) Metabolic Disease (8) Neurological Disease (3)
Click Chemistry:	Azide (3) Alkynes (1)
Oligonucleotides:	Adenosine (1) Nucleotide Analogs (3) Thymine (20) Thymidine (1) siRNA drugs (3) Other Phosphoramidite (1) Antisense Oligonucleotides (5) siRNAs (6) Fluorescent Lipids (1) Pegylated Lipids (3) MicroRNAs (1) Aptamers (4) Nucleoside Analogs (5) Mouse Pre-designed siRNA Sets (2) Cytosine (1) Human Pre-designed siRNA Sets (1) Uracil (6) Phosphoramidites (28)

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Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-130604

DT2216 2 Publications Verification	Bcl-2 Family PROTACs Apoptosis	Cancer
DT2216 is a potent and selective BCL-XL (Bcl-2 family member) degrader based on PROTAC technology. DT2216 causes effective degradation of BCL-XL protein by recruiting Von Hippel-Lindau (VHL) E3 ubiquitin ligase. DT2216 inhibits various BCL-XL-dependent leukemia and cancer cells but considerably less toxic to platelets. DT2216 is composed of the Bcl-2 family protein inhibitor Navitoclax-piperazine (HY-44432), a linker, and a VHL E3 ubiquitin ligase (Pink: Navitoclax-piperazine; Blue: VHL ligand; Black: linker) .

HY-132591

Inclisiran Maximum Cited Publications 7 Publications Verification ALN-PCSsc	PCSK9 Small Interfering RNA (siRNA) Pyroptosis PPAR NOD-like Receptor (NLR) Caspase Interleukin Related	Cardiovascular Disease Metabolic Disease
Inclisiran is a double-stranded small interfering RNA (siRNA) molecule. Inclisiran inhibits the transcription of PCSK9. Inclisiran inhibits Pyroptosis, activates PPARγ, and reduces NLRP3, cleaved caspase-1, IL-1β, and IL-18. Inclisiran has anti-inflammatory, lipid-regulating and anti-atherosclerotic activities. Inclisiran can be used in researches of hyperlipidemia and cardiovascular disease (CVD) .

HY-132609

Patisiran sodium 1 Publications Verification	Small Interfering RNA (siRNA) Transthyretin (TTR)	Neurological Disease
Patisiran sodium is a double-stranded small interfering RNA that targets a sequence within the transthyretin (TTR) messenger RNA. Patisiran sodium specifically inhibits hepatic synthesis of mutant and wild-type TTR. Patisiran sodium can be used for the research of hereditary TTR amyloidosis .

HY-147080

Avacincaptad pegol sodium ARC1905	Complement System	Others
Avacincaptad pegol (ARC1905) sodium is a 40KDa PEG-conjugated aptamer. Avacincaptad pegol sodium targets complement factor 5 (C5), inhibits the cleavage of C5 into C5a and C5b, limits inflammatory stimulation and complement membrane attack complex (MAC), and is used to study age-related macular degeneration (AMD). Avacincaptad pegol sodium limits irregular cell apoptosis by targeting downstream factors in the complement cascade while preserving the early steps of the complement system .

HY-112929

DT-061 Maximum Cited Publications 19 Publications Verification	Phosphatase	Cancer
DT-061 is an orally bioavailable activator of protein phosphatase 2A (PP2A) and could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis .

HY-20140

5'-O-DMT-dT 5'-O-(4,4'-Dimethoxytrityl)thymidine	Phosphoramidites DNA/RNA Synthesis Nucleoside Antimetabolite/Analog	Others
5'-O-DMT-dT (5'-O-(4,4'-Dimethoxytrityl)thymidine) is a nucleoside derivative which can be used in the preparation of oligonucleotides .

HY-W013068

DMT-dT Phosphoramidite	Phosphoramidites DNA/RNA Synthesis	Others
DMT-dT Phosphoramidite is typically used in the synthesis of DNA .

HY-44432

Navitoclax-piperazine ABT-263-piperazine	Ligands for Target Protein for PROTAC Bcl-2 Family	Cancer
Navitoclax-piperazine (ABT-263-piperazine) is a Navitoclax (HY-10087) analog and BCL-XL inhibitor. Navitoclax-piperazine is the ligand for target protein of PROTAC DT2216 (HY-130604). Navitodax-pperaie and E3 ubiquitin ligase VHL ligand can be used to synthesize PROTAC DT2216 (HY-130604) .

HY-P99245

Emactuzumab RG 7155; RO 5509554	c-Fms	Cancer
Emactuzumab(RG 7155) is a specific monoclonal antibody that inhibits colonystimulating factor 1 receptor (CSF1R) activation. Emactuzumab has high affinity for CSF-1R with K_i value of 0.2 nM to blocks CSF-1R dimerization. Emactuzumab can be used for the research of several diseases, such as diffuse-type tenosynovial giant cell tumour (dt-GCT) .

HY-120272

SMAP-2 1 Publications Verification DT-1154	Phosphatase	Cancer
SMAP-2 (DT-1154) is an orally active protein phosphatase 2A (PP2A) activator, with anti-cancer activity .

HY-145720

Cemdisiran ALN-CC5	Complement System Small Interfering RNA (siRNA)	Metabolic Disease
Cemdisiran (ALN-CC5) is an N-acetylgalactosamine-conjugated RNAi agent and also a complement component C5 inhibitor. Cemdisiran targets C5 mRNA, cleaves C5 mRNA via the endogenous RNA interference pathway, and inhibits the production of C5 protein in the liver. Cemdisiran exerts a dose-dependent inhibitory effect on total C5 concentrations in cynomolgus monkeys. When used in combination with Pozelimab (HY-P99786) in cynomolgus monkeys, Cemdisiran achieves a more sustained and complete inhibitory effect on complement activity. Cemdisiran can be used in the research of paroxysmal nocturnal hemoglobinuria and other complement-mediated diseases .

HY-132581

Tadnersen 1 Publications Verification BIIB078; IONIS-C9Rx	Ras Others	Neurological Disease
Tadnersen (BIIB078), an antisense oligonucleotide (ASO), selectively targets *C9ORF72* transcript variants 1 and 3 that carry the expansion .

HY-148457

Avacincaptad pegol Izervay	Complement System	Infection Neurological Disease Inflammation/Immunology
Avacincaptad pegol (Izervay) is a selective inhibitor targeting complement component C5, and is a pegylated ribonucleic acid aptamer. Avacincaptad pegol inhibits the cleavage of C5 into pro-inflammatory C5a and C5b, which forms the membrane attack complex (C5b-9), thereby reducing inflammatory cell recruitment and retinal cell damage. Avacincaptad pegol can slow the growth of geographic atrophy (GA) lesions and reduce the risk of persistent vision loss. Avacincaptad pegol can be used in research of geographic atrophy associated with age-related macular degeneration (AMD) and has been approved by the FDA .

HY-A0152

D-Thyroxine D-T4	Endogenous Metabolite	Metabolic Disease
D-Thyroxine (D-T4) is an orally active thyroid hormone that inhibits the secretion of TSH. D-Thyroxine can inhibit goiter, promote metamorphosis of tadpoles and influence cholesterol metabolism. D-Thyroxine can be used for the study of hypercholesterolemia .

HY-109561

Pegaptanib sodium EYE001; NX1838	VEGFR	Metabolic Disease Inflammation/Immunology
Pegaptanib sodium is an RNA aptamer with polyethylene glycol modifications, which is directed against vascular endothelial growth factor (VEGF)-165. Pegaptanib could be used for the study of neovascular age-related macular degeneration (AMD) .

HY-124801

ABMA 1 Publications Verification	Flavivirus Dengue Virus Bacterial Parasite	Infection
ABMA is a broad-spectrum inhibitor of intracellular toxins and pathogens. ABMA efficiently protects cells against various toxins and pathogens including viruses, intracellular bacteria and parasite. ABMA selectively acts at host cell late endosomes rather than targeting toxin or pathogen itself. ABMA has broad-spectrum anti-infection activity .

HY-B1991

Terbutryn	Environmental Pollutants Herbicide	Others
Terbutryn is a photosystem II inhibitor and aquatic toxicant. Terbutryn interferes with photosynthesis by inhibiting photosystem II. Terbutryn reduces the production of periphyton by acting directly on periphytic algae in artificial indoor streams. Terbutryn reduces the population growth of Lumbriculus variegatus in artificial indoor streams through indirect effects associated with the reduction of food sources for periphyton. The overall 50% dissipation time (DT₅₀) of Terbutryn in the water of artificial indoor streams is 28 d .

HY-P2692B

DT-2 acetate 1 Publications Verification	PKG	Cancer
DT-2 is a potent and selective inhibitor of the cGMP-dependent protein kinase (PKG). DT-2 inhibits PKG catalyzed phosphorylation (K_i: 12.5 nM) .

HY-P0142A

DT-3 acetate	PKG	Cardiovascular Disease
DT-3 acetate is a membrane-permeable protein kinase G Iα (PKG Iα) inhibitory peptide and shows pharmacological blockade of the cGMP-PKG signalling .

HY-138646

Poly(deoxyadenylic-thymidylic) acid sodium 4 Publications Verification Poly(dA:DT) sodium	Cyclic GMP-AMP Synthase STING	Inflammation/Immunology
Poly(deoxyadenylic-thymidylic) acid (Poly(dA:dT)) sodium is a double-stranded DNA stimulant. Poly(deoxyadenylic-thymidylic) acid sodium is recognized by the intracellular DNA sensor DDX41 and activates the innate immune pathway via the adaptor protein STING, inducing the production of cytokines such as type I interferons. Poly(deoxyadenylic-thymidylic) acid sodium also serves as an in vitro transcription template for free RNA polymerase .

HY-156512

DT-6	TGF-beta/Smad	Cancer
DT-6 is an effective TGF-β1 inhibitor. DT-6 inhibits M2 macrophage induced epithelial to mesenchymal transition and invasive migration of cancer cells. DT-6 can be used for cancer diseases research .

HY-W048513

7-Deaza-2'-deoxyadenosine	DNA/RNA Synthesis	Cancer
7-Deaza-2'-deoxyadenosine is an isosteric dATP analog of 2'-deoxyadenosine. 7-Deaza-2'-deoxyadenosine is recognized by various DNA polymerases and incorporated into DNA strands as a substrate. 7-Deaza-2'-deoxyadenosine undergoes a bioorthogonal inverse electron demand Diels-Alder reaction with tetrazine-modified molecules, enabling site-specific labeling of DNA, surface antibody immobilization and intracellular fluorescent labeling. 7-Deaza-2'-deoxyadenosine reduces the DNA curvature of d(A₆)·d(T₆) fragments and the stability of DNA/RNA double helices, and leads to decreased antisense activity against SV40 T Antigen. 7-Deaza-2'-deoxyadenosine finds application in the research field of SV40 T Antigen-related cancers .

HY-132598

Miravirsen SPC-3649	MicroRNA HCV	Infection Inflammation/Immunology
Miravirsen (SPC-3649) is a potent miR-122 inhibitor and inhibits the biogenesis of miR-122. Miravirsen is a 15-nucleotide locked nucleic acid-modified phosphorothioate antisense oligonucleotide. Miravirsen inhibits HCV replication. Miravirsen can be used in research of HCV infection .

HY-130849

(S,R,S)-AHPC-Me-C5-COOH	E3 Ligase Ligand-Linker Conjugates	Cancer
(S,R,S)-AHPC-Me-C5-COOH is a synthesized E3 ligase ligand-linker conjugate that incorporates the a VHL ligand and a linker. (S,R,S)-AHPC-Me-C5-COOH can be used in PROTAC DT2216 (HY-130604) .

HY-W419589

Xanthomicrol	COX NO Synthase Interleukin Related Reactive Oxygen Species (ROS)	Inflammation/Immunology Cancer
Xanthomicrol is extracted from the resin of the plant called Chinese bellflower (a member of the Scrophulariaceae family) and is a monoamine oxidase (MAOs) inhibitor. Xanthomicrol has anti-tumor and anti-inflammatory properties, with IC₅₀ values of 0.88 and 1.69 μg/mL in HL60 and K562 cells. Xanthomicrol's the main metabolite of 5DT in mouse colon, and it can reduce levels of iNOS protein and mRNA, as well as COX-2 protein levels. Additionally, Xanthomicrol decreases the production of the pro-inflammatory cytokine IL-1β and induces the expression of the antioxidant enzyme HO-1 .

HY-P0142

DT-3	PKG	Cardiovascular Disease
DT-3 is a membrane-permeable protein kinase G Iα (PKG Iα) inhibitory peptide and shows pharmacological blockade of the cGMP-PKG signalling .

HY-138597

5'-O-TBDMS-dT	DNA/RNA Synthesis Nucleoside Antimetabolite/Analog	Infection Cancer
5'-O-TBDMS-dT is a nucleoside with protective and modification effects.

HY-164181

Fmoc-protected DMT-Dt PEG2 NH2 amidite	DNA/RNA Synthesis Phosphoramidites	Cancer
Fmoc-protected DMT-Dt PEG2 NH2 amidite is a phosphoramidite monomer.

HY-147079

Egaptivon pegol ARC 1779	Integrin	Cardiovascular Disease
Egaptivon pegol (ARC1779) is an aptamer, which blocks binding of the von Willebrand Factor (VWF) to platelet GPIb receptors. Egaptivon pegol has anti-thrombotic efficacy.

HY-132600

RG-101 Temavirsen	MicroRNA HCV	Infection
RG-101 is a hepatocyte targeted N-acetylgalactosamine conjugated oligonucleotide that antagonises miR-122. miR-122 is an important host factor for hepatitis C virus (HCV) replication .

HY-W700549

DMT-dT	Phosphoramidites Nucleoside Antimetabolite/Analog	Others
DMT-dT is a nucleotide derivative .

HY-177023

Ap5dT	Nucleoside Antimetabolite/Analog	Cancer
Ap5dT is a cytosolic thymidine kinase and mitochondrial enzyme inhibitor with K_is of 0.12 μM and 0.50 μM, respectively. Ap5dT can be used for the study of acute myelocytic leukemia .

HY-177631

Etidaligide DT01; coDbait	Poly(ADP-ribose) Glycohydrolase (PARG)	Cancer
Etidaligide, an AsiDNA, a first-in-class DNA repair inhibitor designed to prevent the repair of DNA damage in tumour cells. It also activates DNA-dependent protein kinase (DNA-PK) and poly (ADP-ribose) polymerase enzymes that induce phosphorylation of H2A

HY-177631A

Etidaligide sodium DT01 sodium; coDbait sodium	Poly(ADP-ribose) Glycohydrolase (PARG)	Cancer
Etidaligide sodium, an AsiDNA, a first-in-class DNA repair inhibitor designed to prevent the repair of DNA damage in tumour cells. It also activates DNA-dependent protein kinase (DNA-PK) and poly (ADP-ribose) polymerase enzymes that induce phosphorylation

HY-173452

DT-23	Fungal	Infection
DT-23 is a potent antifungal agent with an MIC₅₀ of 15 μg/mL. DT-23 inhibits recombinant Arg1 and Kcs1 with IC₅₀s of 0.6 and 0.68 μM, respectively .

HY-W013068S3

DMT-dT Phosphoramidite-d11	Isotope-Labeled Compounds DNA/RNA Synthesis	Others
DMT-dT Phosphoramidite-d₁₁ is deuterium labeled DMT-dT Phosphoramidite (HY-W013068). DMT-dT Phosphoramidite is typically used in the synthesis of DNA.

HY-W013068S2

DMT-dT Phosphoramidite-13C	Isotope-Labeled Compounds DNA/RNA Synthesis	Others
DMT-dT Phosphoramidite- ¹³C is ¹³C-labeled DMT-dT Phosphoramidite (HY-W013068). DMT-dT Phosphoramidite is typically used in the synthesis of DNA.

HY-W013068S1

DMT-dT Phosphoramidite-15N2	Isotope-Labeled Compounds DNA/RNA Synthesis	Others
DMT-dT Phosphoramidite- ¹⁵N₂ is the ¹⁵N labeled DMT-dT Phosphoramidite . DMT-dT Phosphoramidite is typically used in the synthesis of DNA .

HY-161436

TPA-dT	Small Interfering RNA (siRNA)	Others
TPA-dT is a thymidine analog with a tris[(2-pyridyl)methyl]amine (TPA) group. TPA-dT can be used to modify siRNAs. The TPA-modified siRNAs remain functionally inactive and is incapable of silencing gene expression until the TPA moiety is removed upon exposure to Cu(I) .

HY-112929B

(1S,2S,3R)-DT-061 1 Publications Verification	Phosphatase	Cancer
(1S,2S,3R)-DT-061 is an enantiomer of DT-061 (HY-112929). DT-061 is an orally active activator of protein phosphatase 2A (PP2A). (1S,2S,3R)-DT-061 can be used as a negative control in the research of KRAS-mutant and MYC-driven lung cancer tumorigenesis .

HY-W013068S

DMT-dT Phosphoramidite-13C10,15N2	Isotope-Labeled Compounds DNA/RNA Synthesis	Others
DMT-dT Phosphoramidite- ¹³C₁₀, ¹⁵N₂ is the ¹³C and ¹⁵N labeled DMT-dT Phosphoramidite . DMT-dT Phosphoramidite is typically used in the synthesis of DNA .

HY-D1901

FAM-dT phosphoramidite	Fluorescent Dye	Others
FAM-dT phosphoramidite (Compound 21) is a fully protected labelled nucleoside phosphoramidite that can be incorporated into oligonucleotides .

HY-179677

DSPE-PEG2000-Mal-Cys-DT7	Liposome	Others
DSPE-PEG2000-Mal-Cys-DT7 is a phospholipid-PEG conjugate. DSPE-PEG2000-Mal-Cys-DT7 utilizes the amphiphilicity of DSPE to insert into the lipid bilayer of liposomes or nanoparticles.

HY-179677A

DSPE-PEG3400-Mal-Cys-DT7	Liposome	Others
DSPE-PEG3400-Mal-Cys-DT7 is a phospholipid-PEG conjugate. DSPE-PEG3400-Mal-Cys-DT7 utilizes the amphiphilicity of DSPE to insert into the lipid bilayer of liposomes or nanoparticles.

HY-168345A

Ap4dT	DNA/RNA Synthesis	Others
Ap4dT is an inhibitor for human adenylate kinase isozyme 1 (hAK1), that inhibits the ATP and ADP synthesis with IC₅₀s of 42 μM and 38 μM .

HY-168345

Ap4dT tetraammonium	DNA/RNA Synthesis	Others
Ap4dT is an inhibitor for human adenylate kinase isozyme 1 (hAK1), that inhibits the ATP and ADP synthesis with IC₅₀s of 42 μM and 38 μM .

HY-147265

Eldocasiran	MicroRNA	Cancer
Eldocasiran is a micro-ARN-193a-3p analogue, Eldocasiran has anticancer activity. Eldocasiran can be used for cancer research .

HY-E70739

KIT V559D/T670I Recombinant Human Active Protein Kinase	c-Kit	Cancer
KIT (CD117) is an important cell surface marker used to identify certain types of hematopoietic(blood) progenitors in the bone marrow. KIT is a cytokine receptor expressed on the surface of hematopoietic stem cells as well as other cell types. Altered forms of this receptor may be associated with some types of cancer. KIT V559D/T670I is a mutant of KIT. KIT V559D/T670I Recombinant Human Active Protein Kinase is a recombinant KIT V559D/T670I protein that can be used to study KIT V559D/T670I-related functions .

HY-P11298

d-T101 peptide	Caspase Apoptosis JNK p38 MAPK Interleukin Related IFNAR	Inflammation/Immunology Cancer
d-T101 peptide, a human hormone-peptide, is a T1/ST2 receptor ligand. d-T101 peptide binds to the T1/ST2 receptor and activates caspases 8, 9 and 3 mediated apoptosis, together with activation of JNKinase and p38 MAPKinase. d-T101 peptide also changes Golgi structural with function loss and downregulation of the endoplasmic reticulum (ER) stress repair mechanism. d-T101 peptide has immunostimulatory and anticancer activity, selectively induces apoptosis in proliferating cancer cells and increases IL-2 and IFN-γ expression as well as the recruitment of NK cells and M1 macrophages to the tumor site .

HY-123400A

iso-Samixogrel iso-DTTX30; iso-DT-TX 30 SE	Prostaglandin Receptor	Cardiovascular Disease
Iso-Samixogrel (iso-DTTX30) is a combined thromboxane A2 receptor blocker and thromboxane synthetase inhibitor that exhibits potent antithrombotic activity. Iso-Samixogrel effectively eliminates recurrent arterial thrombus formation and inhibits collagen-induced platelet aggregation ex vivo. Iso-Samixogrel also prolongs sublingual bleeding time, demonstrating its biological efficacy in managing thrombosis.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-A0152

D-Thyroxine D-T4	Ketones, Aldehydes, Acids Metabolic Disease Endogenous metabolite Disease Research Fields Source Classification	Endogenous Metabolite
D-Thyroxine (D-T4) is an orally active thyroid hormone that inhibits the secretion of TSH. D-Thyroxine can inhibit goiter, promote metamorphosis of tadpoles and influence cholesterol metabolism. D-Thyroxine can be used for the study of hypercholesterolemia .

HY-A0152R

D-Thyroxine (Standard) D-T4 (Standard)	Ketones, Aldehydes, Acids Endogenous metabolite Source Classification	Reference Standards Endogenous Metabolite
D-Thyroxine (Standard) is the analytical standard of D-Thyroxine (HY-A0152). This product is intended for research and analytical applications. D-Thyroxine (D-T4) is an orally active thyroid hormone that inhibits the secretion of TSH. D-Thyroxine can inhibit goiter, promote metamorphosis of tadpoles and influence cholesterol metabolism. D-Thyroxine can be used for the study of hypercholesterolemia .

Cat. No.	Product Name	Chemical Structure

HY-W013068S3

DMT-dT Phosphoramidite-d11
DMT-dT Phosphoramidite-d₁₁ is deuterium labeled DMT-dT Phosphoramidite (HY-W013068). DMT-dT Phosphoramidite is typically used in the synthesis of DNA.

HY-W013068S2

DMT-dT Phosphoramidite-13C
DMT-dT Phosphoramidite- ¹³C is ¹³C-labeled DMT-dT Phosphoramidite (HY-W013068). DMT-dT Phosphoramidite is typically used in the synthesis of DNA.

HY-W013068S1

DMT-dT Phosphoramidite-15N2
DMT-dT Phosphoramidite- ¹⁵N₂ is the ¹⁵N labeled DMT-dT Phosphoramidite . DMT-dT Phosphoramidite is typically used in the synthesis of DNA .

HY-W013068S

DMT-dT Phosphoramidite-13C10,15N2
DMT-dT Phosphoramidite- ¹³C₁₀, ¹⁵N₂ is the ¹³C and ¹⁵N labeled DMT-dT Phosphoramidite . DMT-dT Phosphoramidite is typically used in the synthesis of DNA .

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Species:	Human (3) Mouse (2) Cynomolgus (1) Canine (1)
Tag:	SUMO (2) His (7)
Source:	HEK293 (1) P. pastoris (2) E. coli (4)


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Host:	Mouse (3) Rabbit (3)
Reactivity:	Human (6) Rat (4) Mouse (4)
Application:	IHC-P (6) ICC/IF (1) IP (1) WB (2) ELISA (1)
Isotype:	IgG (3) IgG1 (2)
Conjugation:	Non-conjugated (6)
Clonality:	Monoclonal (4) Recombinant (1)
Modification:	Unmodified (4)


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DT

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