CBX1 / HP1-Beta Peptide Reference: ARG56408 This gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family . The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N-terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C-terminal chromo shadow-domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin-associated nonhistone proteins. The protein may play an important role in the epigenetic control of chromatin structure and gene expression. Several related pseudogenes are located on chromosomes 1, 3, and X. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
Z-VEID-FMK Reference: HY-P1007 Z-VEID-FMK is a selective inhibitor of caspase-6. Z-VEID-FMK can be used for the research of tumor.
Hexa-His TFA Reference: HY-P0294A Hexa-His TFA is a peptide consisting of 6 His residues, used as a metal binding site for the recombinant protein.
(R)-2-Amino-2-(4-fluorophenyl)acetic acid Reference: HY-W051418 (R)-2-Amino-2-(4-fluorophenyl)acetic acid is a Glycine (HY-Y0966) derivative.
Insulin icodec Reference: HY-P4070 Insulin icodec is a basal insulin analog. Insulin icodec can be used for the research of type 2 diabetes.
mTRP-2 (180-188) Reference: HY-P1827 mTRP-2 (180-188) is a murine tyrosinase-related protein 2 (TRP-2) -derived peptide, corresponding to residues 180-188. TRP-2 (180-188) is identified as the major reactive epitope within TRP-2 recognized by anti-B16 CTLs.
Shepherdin (79-87) Reference: HY-P1750 Shepherdin (79-87) is amino acids 79 to 87 fragment of Shepherdin. Shepherdin is a peptidomimetic antagonist of the complex between Hsp90 and Survivin. Anticancer activity.
Human PD-L1 inhibitor I Reference: HY-P2474 Human PD-L1 inhibitor I is a hPD-1 peptide ligand, with a KD of 3.39 μM. Human PD-L1 inhibitor I may disturb the binding of hPD-L1 to hPD-1.
K41498 Reference: HY-P1106 K41498 is a potent and highly selective CRF2 receptor antagonist with Ki values of 0.66 nM, 0.62 nM and 425 nM for human CRF2α, CRF2β and CRF1 receptors respectively. K41498 is an analogues of antisauvagine-30 (aSvg-30), inhibits sauvagine-stimulated cAMP accumulation in hCRF2α- and hCRF2β-expressing cells. K41498 can be used for hypotension study.
(R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid Reference: HY-W014258 (R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid is a Glycine (HY-Y0966) derivative.