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M2206 TH-302 (Evofosfamide) TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM.
M6098 Baicalein Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM.
M9325 EGTA EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages.
M9330 Brij-35 Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability.
M6154 2-PMPA tetrasodium 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM.
M2250 Pamidronate disodium Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis.
M9916 DPPH DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants.
M9194 Insulin (human) Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets.
M3409 Formestane Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM.
M9665 N-(2-amino-2-oxoethyl)acrylamide N-(2-Amino-2-oxoethyl)acrylamide
M52930 [Arg-15, 20, 21, Leu17]-PACAP-Gly-Lys-Arg-NH2 [Arg-15,-20,-21,Leu17]-PACAP-Gly-Lys-Arg-NH2 (BM-PACAP) is a synthetic PACAP 1-27 analogue with relaxant effect.
M52929 PACAP-38 (16-38), human, mouse, rat PACAP-38 (16-38), human, mouse, rat demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production.
M52928 PACAP (6-38), human, ovine, rat PACAP (6-38), human, ovine, rat is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.
M52927 PACAP (1-38) free acid PACAP (1-38) free acid is an endogenous neuropeptide.
M52909 Osteostatin (1-5) amide (human, bovine, dog, horse, mouse, rabbit, rat) Osteostatin (1-5) amide (human, bovine, dog, horse, mouse, rabbit, rat) (Human PTHrP (107-111) amide) is a C-terminal parathyroid hormone-related protein fragment that can inhibit bone resorption.
M52908 Osteostatin Osteostatin, a fragment of parathyroid hormone-related protein (PTHrP) 107-111, promotes bone repair in animal models of bone defects and prevents bone erosion in inflammatory arthritis.
M52903 Relaxin H3 (human) Relaxin H3 (human) is a kind of relaxin peptide.
M52902 Secretin (28-54), human Secretin (28-54), human is a 27-amino acid residue C-terminally amidated peptide, which acts on human secretin receptors.
M52901 Secretin, porcine Secretin, porcine (Porcine secretin acetate) is a 27-amino acid peptide, acting on pancreatic acinar cells and ductal epithelial cells stimulating the production of bicarbonate rich fluid.
M52885 [Orn5]-URP [Orn5]-URP is a potent and selective pure antagonist of Urotensin-II receptor (UT), with an pEC50 of 7.24.
M52883 Urotensin II, mouse Urotensin II, mouse is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR.
M52882 UFP-803 UFP-803 is a potent urotensin-II receptor (UT) ligand.
M52881 [Orn8]-Urotensin II (human) [Orn8]-Urotensin II (human), a peptide analog of urotensin II, is a UT receptor agonist.
M52857 IFN-α Receptor Recognition Peptide 1 IFN-α Receptor Recognition Peptide 1 is a peptide of IFN-α associated with receptor interactions.
M52848 KKI-5 KKI-5 is a specific inhibitor of tissue kallikrein.
M52847 D-Val-Leu-Arg-pNA acetate D-Val-Leu-Arg-pNA (acetate) is the acetate form of D-Pro-Phe-Arg-p-nitroanilide (pNa).
M52839 Prostate Specific Antigen Substrate Prostate Specific Antigen Substrate is a prostate specific antigen (PSA) fluorescent substrate.
M52792 Calmodulin-Dependent Protein Kinase II (281-309) Calmodulin-Dependent Protein Kinase II (281-309) is a peptide of calcium/calmodulin-dependent protein kinase II (CaM-kinase II).
M52791 Calmodulin Binding Peptide 1 Calmodulin Binding Peptide 1 is a high affinity (pM) CaM-binding peptide derived from smooth muscle myosin light-chain kinase (MLCK peptide), which strongly inhibits IP3-induced Ca2+ release .
M52790 CALP2 CALP2 is a calmodulin (CaM) antagonist ( (Kd of 7.9 µM)) with high affinity for binding to the CaM EF-hand/Ca2+-binding site.




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