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Peptides

Cat.No.  Name Information
M45271 Ganirelix acetate Ganirelix acetate is a competitive gonadotropin-releasing hormone (GnRH) antagonist that directly binds to endogenous molecules competing for the receptor and causes a rapid decrease in estradiol levels. Ganirelix acetate can be used in studies related to ovarian hyperstimulation syndrome (OHSS) and preterm labor.
M45233 Foxy-5 Foxy-5, a WNT5A agonist and a mimetic peptide of WNT5A, triggers cytoplasmic free calcium signaling without affecting β-catenin activation and inhibits migration and invasion of epithelial cancer cells.Foxy-5 effectively reduces metastatic spread of prostate cancer cells with low WNT5A expression in an in situ mouse model.
M45208 GIP, human GIP, human is a peptide hormone consisting of 42 amino acids that also acts as a promoter of glucose-dependent insulin secretion and a weak inhibitor of gastric acid secretion. In addition, GIP, human acts as an enteric proinsulin hormone released by intestinal K cells in response to nutrient intake.
M45189 L-Leucyl-L-proline hydrochloride L-Leucyl-L-proline hydrochloride is a dipeptide.
M45169 C-Peptide TFA C-Peptide TFA is a component of insulinogen, which is released into the bloodstream from pancreatic islet B cells along with insulin.
M45167 Liraglutide Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that may be used in studies related to type 2 diabetes.
M45044 Alloferon 1 acetate Alloferon 1 acetate is a peptide isolated from the immune system of insects with anti-inflammatory, anti-tumor and anti-viral activities.
M43968 EPQpYEEIPIYL EPQpYEEIPIYL is a phosphopeptide and ligand for the Src homology 2 (SH2) structural domain that activates Src family members (e.g., Lck, Hck, Fyn) by binding to the SH2 domain.
M43964 Cholecystokinin (26-33), CCK8 TFA Cholecystokinin (26-33), CCK8 TFA is a synthetic desulfated octapeptide cholecystokinin (CCK). Sequence: Asp-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH2
M43930 Dalbavancin hydrochloride Dalbavancin hydrochloride is a semisynthetic lipoglycopeptide antibiotic with potent bactericidal activity against Gram-positive bacteria, and its MIC90 for inhibition of Staphylococcus aureus and Bacillus anthracis was 0.06 μg/mL and 0.25 μg/mL, respectively.
M43916 EPO mimetic peptide-1 EPO mimetic peptide-1 (EMP-1) is a 20 amino acid peptide. EPO mimetic peptide-1 stimulates cell proliferation, affects cell cycle and induces the production of reticulocytes in vivo.
M43911 Tachyplesin I Tachyplesin I is a cationic antimicrobial peptide containing 17 amino acid residues.
M43906 Eneboparatide Eneboparatide is a straight-chain peptide consisting of 36 amino acids and a long-acting parathyroid hormone (PTH1) receptor agonist that restores balanced bone turnover and maintains bone integrity while maintaining calcium homeostasis and normalizing urinary calcium. It can be used in studies related to parathyroid dysfunction.
M43321 FRETS-VWF73 FRETS-VWF73 is a biological active peptide.
M43191 Hexaarginine Hexa-arginine, consisting of six arginines, is a polycationic peptide that can penetrate cells efficiently.
M40759 Human β-defensin 1 Human β-defensin 1 is a member of a family of naturally occurring antimicrobial peptides produced by epithelial cells that have antimicrobial activity and can be used in studies related to autoimmune diseases.
M40732 H-GLU(AMC)-OH TFA H-GLU(AMC)-OH TFA can be used as a substrate to detect glutamyl aminopeptidase activity.
M40731 H-GLU(AMC)-OH H-GLU(AMC)-OH can be used as a substrate to detect glutamyl aminopeptidase activity.
M40668 SFTI-1 SFTI-1 is a head-to-tail bicyclic peptide with a disulfide bond that inhibits the serine protease trypsin with subnanomolar levels of inhibition constants. It can be used as a protease inhibitor or as a molecular grafting scaffold. In addition, by introducing a known tetrapeptide pharmacophore into the bicyclic SFTI-1, a potent ligand for melanocortin can be created.
M40634 Z-ARG-LEU-ARG-GLY-GLY-AMC acetate salt Z-ARG-LEU-ARG-GLY-GLY-AMC acetate salt is a fluorescent peptide substrate that can be used to determine the activity of UCH-L3 and USP-5.

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