125 Results for "

integration

" in MedChemExpress (MCE) Product Catalog:
Products (125)

125 Results for "integration" in MCE Product Catalog:

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1
1 Cited Publications
Cat. No.: HY-P704313
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: WNT5A; Wnt Family Member 5A; HWNT5A; Wingless-Type MMTV integration Site Family, Member 5A; WNT-5A Protein; Protein Wnt-5a; Wingless-Type MMTV integration Site Family Member 5A Variant 2; Epididymis Secretory Sperm Binding Protein; Protein Wnt
Species:  
Mouse
Source:  
E. coli
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1 Cited Publications
Cat. No.: HY-P700065AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF3; Heparin-Binding Growth Factor 3; Prev. INT2; Proto-Oncogene Int-2; HBGF-3; Oncogene INT2; Fibroblast Growth Factor 3 (Murine Mammary Tumor Virus integration Site (V-Int-2) Oncogene Homolog); FGF-3; V-INT2 Murine Mammary Tumor Virus integration Site
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-P701745
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PIM1; Proto-Oncogene Serine/Threonine-Protein Kinase Pim-1; Prev. PIM; Pim-1 Oncogene; Serine/Threonine-Protein Kinase Pim-1; Oncogene PIM1; Pim-1 Proto-Oncogene, Serine/Threonine Kinase; Pim-1 Oncogene (Proviral integration Site 1)
Species:  
Human
Source:  
E. coli
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1 Cited Publications
Cat. No.: HY-N0390S2
CAS No.: 14341-78-7
Synonyms: L-Glutamic acid 5-amide-d5
L-Glutamine-d5 is the deuterium labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na +-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity .
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1 Cited Publications
Cat. No.: HY-N0390S5
CAS No.: 159663-16-8
Synonyms: L-Glutamic acid 5-amide-1-13C
L-Glutamine-1- 13C is the 13C-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na +-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity .
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1 Cited Publications
Cat. No.: HY-N0390S8
CAS No.: 204451-48-9
Synonyms: L-Glutamic acid 5-amide-15N2
L-Glutamine- 15N2 is the 15N-labeled L-Glutamine (HY-N0390). L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. L-Glutamine is taken up in a Na +-dependent manner and targets multiple key molecules including glutaminase, mTORC1, NF-κB, STAT-3 and HIF-1α. L-Glutamine enhances glutaminolytic catabolism, drives the conversion of glutamate to α-ketoglutarate, thereby regulating gene expression, integrating metabolic signals, mediating glutamine flux and maintaining redox homeostasis. L-Glutamine also promotes cell proliferation, osteogenic differentiation and fracture healing, exerts neuroprotective and cardioprotective effects, and inhibits osteoarthritis. L-Glutamine can be applied to research related to osteoporosis, osteoarthritis, ischemic stroke and acute cantharidin-induced cardiotoxicity .
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Cat. No.: HY-160807
CAS No.: 2769152-95-4
Research Areas:  

Cancer

DBM-GGFG-NH-O-CO-Exatecan (Example 4, Compound 14) is a conjugate of an ADC drug toxin molecule and a linker. DBM-GGFG-NH-O-CO-Exatecan is a complete antibody-drug conjugate intermediate that integrates a potent camptothecin-based toxin, a cleavable peptide linker (GGFG), and a reactive terminus that can directly conjugate to antibodies .
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Cat. No.: HY-152073
CAS No.: 2924598-24-1
Purity:  98.76%
Target:  

Fluorescent Dye

Research Areas:  

Others

BETA-1 is the first twisted intramolecular charge transfer (TICT)-aggregation-induced emission (AIE) integration molecule. BETA-1 emits cyan fluorescence in lipid droplets (LDs) and red fluorescence in mitochondria. BETA-1 can be used for the simultaneous and dual-color imaging of LDs and mitochondria in vivo and in vitro .
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Cat. No.: HY-159828
CAS No.: 2568911-72-6
Synonyms: VH-499; VH4011499
Target:  

HIV

Research Areas:  

Infection

Dezecapavir (VH-499) is a HIV-1 capsid protein inhibitor. Dezecapavir exhibits picomolar-level antiviral activity against a variety of HIV-1 laboratory strains and clinical isolates in vitro. Dezecapavir inhibits the early and late stages of the HIV-1 life cycle, blocking nuclear import, reverse transcript production, virion assembly, maturation, and post-nuclear import/pre-integration replication processes. Dezecapavir can be used in studies related to HIV-1 infection .
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Cat. No.: HY-163319
CAS No.: 3032667-94-7
Target:  

ClpP Apoptosis

Research Areas:  

Cancer

NCA029 is a potent and selective homo sapiens caseinolytic protease P (HsClpP) activator with an EC50 of 0.15 μM. NCA029 acts on HsClpP to activate an ATF3-dependent integrative stress response, leading to colon cancer cell death .
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Cat. No.: HY-164574
CAS No.: 2565792-45-0
BCN-DOTA is a cyclooctyne-linked DOTA chelator. BCN-DOTA integrates BCN and DOTA, enabling conjugation with azide-functionalized groups via the click chemistry properties of BCN, while binding to metal ions through the coordination capacity of DOTA. BCN-DOTA can serve as a radionuclide-drug conjugate (RDC) to target specific biomolecules, cells or tissues after radiolabeling with zirconium-89. BCN-DOTA is applicable to research related to PET imaging and targeted therapy .
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Cat. No.: HY-E0225
Target:  

Others

Research Areas:  

Others

The 0.5 mL SBS Rack is a 96-well biobank storage rack suitable for -80°C environments. It can hold 0.5 mL externally threaded cryogenic vials with 2D codes on the bottom, and supports automated sample tracking, detection, and laboratory information system integration. The 0.5 mL SBS Rack can be used with camera-based reading devices to scan and log biobank vials with 2D codes into databases, enabling rapid identification of aliquoted samples .
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Cat. No.: HY-100534
CAS No.: 1136466-93-7
Purity:  ≥99.0%
IDE 2 is a cell-permeable inducer of definitive endoderm differentiation that induces the differentiation of mouse and human embryonic stem cells into definitive endoderm. IDE2 activates the TGF‑β/Nodal signaling pathway, induces Smad2 phosphorylation, and increases Sox17 and FoxA2 expression. Endoderm induced by IDE 2 integrates into the developing gut tube, expresses gut tube markers, and differentiates into pancreatic progenitor cells. IDE 2 can be used for research related to directed endoderm differentiation of embryonic stem cells .
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Cat. No.: HY-177119
Research Areas:  

Infection

ZBP1 Covalent PROTAC-1 is a covalent PROTAC degrader targeting ZBP1, with a DC50 of 25.69 nM. ZBP1 Covalent PROTAC-1 integrates a ZBP1-binding DNA aptamer, a linker containing covalent NASA, and an E3 ligase-recruiting moiety to guide ubiquitin-proteasome system-mediated degradation of ZBP1. ZBP1 Covalent PROTAC-1 exhibits inhibitory activity against necroptosis signaling pathways and inflammatory responses. ZBP1 Covalent PROTAC-1 can be used for research on viral pneumonia .
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Cat. No.: HY-132870
CAS No.: 2761326-86-5
Purity:  99.33%
Target:  

HOXA

Research Areas:  

Others

MEIS-IN-2 is a myeloid ecotropic viral integration site 1 (MEIS1) inhibitor.
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Cat. No.: HY-108460
CAS No.: 824982-41-4
Purity:  ≥99.0%
Target:  

TRP Channel

Research Areas:  

Neurological Disease

A-784168 is a potent and orally active inhibitor of vanilloid receptor type 1 (TRPV1). Vanilloid receptor type 1 (TRPV1) is a ligand-gated nonselective cation channel that is considered to be an important integrator of various pain stimuli such as endogenous lipids, capsaicin, heat, and low pH. A-784168 has good CNS penetration .
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Cat. No.: HY-125385
CAS No.: 187099-99-6
Purity:  ≥95.0%
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Sulforhodamine 101 DHPE is a fluorescent probe made from the conjugation of the phospholipid 1,2-dipalmitoyl-sn-glycero-3-PE to sulforhodamine 101, a red fluorescent dye that displays excitation/emission spectra of 586/605 nm, respectively. It integrates into phospholipid bilayers and has been used for imaging of solid supported lipid bilayers, detection of protein-ligand binding on bilayers, and to monitor colocalization of lipid probes in liposomes via resonance energy transfer (RET).
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Cat. No.: HY-126967A
CAS No.: 7220-34-0
Purity:  ≥99.0%
Synonyms: 1-P-GPA
1-Palmitoyl-sn-glycerol 3-phosphate (1-P-GPA) is a phospholipid and lipid membrane precursor. 1-Palmitoyl-sn-glycerol 3-phosphate integrates into POPC liposomes, causing significant changes in membrane curvature. 1-Palmitoyl-sn-glycerol 3-phosphate induces platelet aggregation, but its activity is 30-fold lower than that of 1-hexadecyl-sn-glyceryl-3-phosphate .
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Cat. No.: HY-W591393
CAS No.: 2669097-31-6
Biotin Azide Plus is an oxazolidine reagent that integrates azide-biotin click chemistry and a photocleavable linker arm. Biotin Azide Plus not only reacts with biotin thioether to form stable sulfinimide products, but also enables bioconjugation of proteins and DNA through biotin redox-activated chemical labeling technology. Taking advantage of the streptavidin capture and photo-release properties, Biotin Azide Plus effectively facilitates the isolation of lipid-derived electrophile-protein adducts, thus finding wide application in scientific research related to fields such as SKBR3 cancer .
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Cat. No.: HY-151761
CAS No.: 2084913-49-3
Purity:  99.69%
Research Areas:  

Others

H-L-Lys (4-N3-Z)-OH hydrochloride is an unnatural lysine analog and a substrate of the PABKRS mutant PylRS. H-L-Lys (4-N3-Z)-OH hydrochloride enables site-specific genetic integration into proteins via amber stop codon suppression; it undergoes Staudinger reduction with phosphine compounds, followed by a self-elimination reaction to release native lysine. H-L-Lys (4-N3-Z)-OH hydrochloride serves as a genetically encoded element for the temporal chemical control of protein SUMOylation and nuclear translocation in living mammalian cells, and also acts as a bioorthogonal reaction handle for bioconjugation reactions .
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