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 About 12 results found for searched term "CD31" (0.12 seconds)

Cat.No.  Name Target
M6572 CD 2314 Others
CD 2314 is a selective RARβ agonist.
M14592 CDDO-EA Keap1-Nrf2
CDDO ethyl amide; TP319; RTA 405
CDDO-EA is an NF-E2 related factor 2/antioxidant response element (Nrf2/ARE) activator.
M50412 CD31 Others
CD31 (PECAM-1) is platelet endothelial cell adhesion molecule-1, serves as the endothelial cell-specific receptor of clostridium perfringens b-Toxin (CPB).
M55348 5-(chloromethyl)-3-(4-methoxyphenyl)-1,2,4-oxadiazole Screening Compounds and Building Blocks
5-Chloromethyl-3-(4-methoxyphenyl)-[1,2,4]oxadiazole
5-(chloromethyl)-3-(4-methoxyphenyl)-1,2,4-oxadiazole
M14807 Cibinetide Peptides
ARA290
Cibinetide (ARA290) is an EPO-derivative, acting as a specific agonist of erythropoietin/CD131 heteroreceptor, and used for the research of neurological disease.
M21677 Recombinant Human Follistatin 288 (HEK293, C-6His) Cytokines and Growth Factors
FST; follistatin isoform FST317
Follistatin 288 is a secreted glycoprotein that was first identified as a follicle-stimulating hormone inhibiting substance in ovarian follicular fluid . Human follistatin 288 cDNA encodes a 317 amino acid (aa) protein with a 29 aa signal sequence, and a 288 aa mature region. Recombinant Human Follistatin/FST is produced by Mammalian expression system and the target gene encoding Gly30-Asn317 is expressed with a 6His tag at the C-terminus.
M25365 ATG-031 Others
ATG-031 is a humanised anti-CD24 monoclonal antibody. ATG-031 effectively stimulates macrophage-mediated phagocytosis and induces cancer cell destruction by blocking the "don't eat me" signals that characterize the growth of many cancers. ATG-031 can be used in the study of haematological malignancies as well as solid tumours.
M31200 CK7  CDK
CK-7
CK7 is a Cdk2/9 inhibitor, which can be used for the synthesis of Nek1 inhibitor BSc5231 and BSc5367.
M41376 DRI-C21041 TNF Receptor
DRI-C21041 is a CD40/CD40L interaction inhibitor, with an IC50 of 0.31 μM.
M45310 SR-1277 Casein Kinase
SR-1277 is a potent, selective and ATP-competitive CK1δ/ε inhibitor with IC50 values of 49 nM and 260 nM, respectively.In addition, SR-1277 inhibits FLT3, CDK4/cyclin D1, CDK6/cyclin D3, and CDK9/cyclin K with IC50 values of 305 nM, 1340 nM, 311 nM, and 109 nM, respectively. 1340 nM, 311 nM and 109 nM, respectively, and can be used in cancer research.
M54033 P8RI Others
P8RI (D-P8RI) is a biomimetic peptide of CD31 and a CD31 agonist.
M54707 INX-315 CDK
INX-315 is an orally potent and selective CDK2 inhibitor that induces cell cycle arrest in G1 phase. INX-315 also induces CDK2 substrate phosphorylation and inhibits tumor growth in a dose-dependent manner in a xenograft mouse model.INX-315 can be used in cancer-related studies.



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