Rxreliance

GALACTO-RGD. 1mg Radiolabeled analogs of Galacto-RGD are useful for studying expression of +5+3 integrin in tumor cells CAS: 922175-70-0 C34H52N10O12 FW: 792.85 . Synonym: Cyclo(RGDfK(SAA))

GALACTO-RGD. 5mg Radiolabeled analogs of Galacto-RGD are useful for studying expression of +5+3 integrin in tumor cells CAS: 922175-70-0 C34H52N10O12 FW: 792.85 . Synonym: Cyclo(RGDfK(SAA))

SPEXIN. 0.5mg Spexin (SPX, also called NPQ) is a gastro-intestinal peptide hormone. In situ hybridization localized its mRNA to the stomach and esophagus. Synthetic spexin induced dose-dependent contraction of stomach muscle, sug gesting that it is involved in digestion. The results obtained by Rucinski et al. indicate that spexin may inhibit adrenocortical cell proliferation. CAS: 1370290-58-6 C74H114N20O19S FW: 1619.91 . gastrointestinal peptide

SPEXIN. 1mg Spexin (SPX, also called NPQ) is a gastro-intestinal peptide hormone. In situ hybridization localized its mRNA to the stomach and esophagus. Synthetic spexin induced dose-dependent contraction of stomach muscle, sug gesting that it is involved in digestion. The results obtained by Rucinski et al. indicate that spexin may inhibit adrenocortical cell proliferation. CAS: 1370290-58-6 C74H114N20O19S FW: 1619.91 . gastrointestinal peptide

MET-RANTES (HUMAN). 50ug Synthetic product. Potent antagonist of RANTES and macrophage inflammatory polypeptide-1+ (MIP-1+). Met-RANTES inhibited RANTES- or MIP-1+-induced chemotaxis of promonocytic THP-1cells and T-cells. Althoug h Met-RANTES antagonized RANTES and MIP-1+ with similar potency in the chemotaxis response it showed a clear difference in the cytokine-induced calcium mobilization assay. (Disulfide bonds between Cys10 and Cys34/Cys11 and Cys50) C355H543N97O101S6 FW: 7978.21 . RANTES

MET-RANTES (HUMAN). 1mg Synthetic product. Potent antagonist of RANTES and macrophage inflammatory polypeptide-1+ (MIP-1+). Met-RANTES inhibited RANTES- or MIP-1+-induced chemotaxis of promonocytic THP-1cells and T-cells. Althoug h Met-RANTES antagonized RANTES and MIP-1+ with similar potency in the chemotaxis response it showed a clear difference in the cytokine-induced calcium mobilization assay. (Disulfide bonds between Cys10 and Cys34/Cys11 and Cys50) C355H543N97O101S6 FW: 7978.21 . RANTES

(GLU13-+17-+20)-OSTEOCALCIN (1-46) . 0.5mg (Disulfide bond) C226H351N57O74S2 FW: 5114.75 . osteocalcin

(GLU13-+17-+20)-OSTEOCALCIN (1-46) . 1mg (Disulfide bond) C226H351N57O74S2 FW: 5114.75 . osteocalcin

PREPTIN (RAT). 0.5mg Preptin is a 34-amino acid peptide hormone, which is co-secreted with insulin from the pancreatic +-cells in response to glucose stimulation. It is osteogenic in vitro and in vivo and may act in concert with the other +-cell hormones insulin and amylin to stimulate bone formation in hyperinsulinemic states such as obesity. CAS: 315197-73-0 C181H268N48O51 FW: 3932.41 . preptin

PREPTIN (RAT). 1mg Preptin is a 34-amino acid peptide hormone, which is co-secreted with insulin from the pancreatic +-cells in response to glucose stimulation. It is osteogenic in vitro and in vivo and may act in concert with the other +-cell hormones insulin and amylin to stimulate bone formation in hyperinsulinemic states such as obesity. CAS: 315197-73-0 C181H268N48O51 FW: 3932.41 . preptin

ALARIN (HUMAN). 0.5mg Alarin, APAHRSSTFPKWVTKTERGRQPLRS, is derived from a splice variant of galanin-like peptide (GALP) RNA. It shows potent and dose-dependent vasoconstrictor and anti-edema activity in the cutaneous microvasculature, as was also observed with other members of the galanin peptide family. Since alarin only shares five amino acids with GALP it is unlikely that the peptide can activate GALP-specific receptors. The neuropeptide has been reported to be expressed in ganglionic cells of human neuroblastic tumors and might therefore represent a potential tumor marker. CAS: 909409-86-5 C127H205N43O35 FW: 2894.29 . alarin

ALARIN (HUMAN). 1mg Alarin, APAHRSSTFPKWVTKTERGRQPLRS, is derived from a splice variant of galanin-like peptide (GALP) RNA. It shows potent and dose-dependent vasoconstrictor and anti-edema activity in the cutaneous microvasculature, as was also observed with other members of the galanin peptide family. Since alarin only shares five amino acids with GALP it is unlikely that the peptide can activate GALP-specific receptors. The neuropeptide has been reported to be expressed in ganglionic cells of human neuroblastic tumors and might therefore represent a potential tumor marker. CAS: 909409-86-5 C127H205N43O35 FW: 2894.29 . alarin

LABRADIMIL. 1mg Labradimil , Arg-Pro-Hyp-Gly-Thi-Ser-Pro-Tyr(Me)-psi(CH2NH)-Arg, is a selective bradykinin B2 receptor agonist with a longer plasma half-life than bradykinin. Labradimil transiently increases the permeability of the blood-brain barrier (BBB) to facilitate delivery of drug s to the CNS. CAS: 159768-75-9 C49H75N15O12S FW: 1098.29 . Synonym: Labradimil, Lobradimil, RMP-7

PSEUDIN-2. 1mg Pseudin-2 is a cationic +-helical peptide originally isolated from the skin of the paradoxical frog Pseudis paradoxa on the basis of its antimicrobial activity. GLNALKKVFQGIHEAIKLINNHVQ stimulated insulin secretion from BRIN-BD11 cells by a Ca2+-independent mechanism. C122H202N36O32 FW: 2685.17 . pseudin

PSEUDIN-2. 5mg Pseudin-2 is a cationic +-helical peptide originally isolated from the skin of the paradoxical frog Pseudis paradoxa on the basis of its antimicrobial activity. GLNALKKVFQGIHEAIKLINNHVQ stimulated insulin secretion from BRIN-BD11 cells by a Ca2+-independent mechanism. C122H202N36O32 FW: 2685.17 . pseudin

ANGIOTENSIN (1-12) (HUMAN). 1mg DRVYIHPFHLVI, an angiotensin peptide. Angiotensin 1-12 is cleaved in human cardiac tissue by chymase yielding angiotensin II. CAS: 136865-09-3 C73H109N19O16 FW: 1508.79 . Synonym: Angiotensinogen (1-12) (human), Proangiotensin-12 (human)

ANGIOTENSIN (1-12) (HUMAN). 5mg DRVYIHPFHLVI, an angiotensin peptide. Angiotensin 1-12 is cleaved in human cardiac tissue by chymase yielding angiotensin II. CAS: 136865-09-3 C73H109N19O16 FW: 1508.79 . Synonym: Angiotensinogen (1-12) (human), Proangiotensin-12 (human)

GASTRIC INHIBITORY POLYPEPTIDE (3. 0.5mg Gastric inhibitory polypeptide (3-42) represents the major physiological degradation product of gastric inhibitory polypeptide (GIP). It is generated by proteolytic processing of GIP by dipeptidyl peptidase IV (DPP IV). C214H324N58O63S FW: 4749.35 . Synonym: GIP (3-42) (human), Glucose-Dependent Insulinotropic Polypeptide (3-42) (human)

GASTRIC INHIBITORY POLYPEPTIDE (3. 1mg Gastric inhibitory polypeptide (3-42) represents the major physiological degradation product of gastric inhibitory polypeptide (GIP). It is generated by proteolytic processing of GIP by dipeptidyl peptidase IV (DPP IV). C214H324N58O63S FW: 4749.35 . Synonym: GIP (3-42) (human), Glucose-Dependent Insulinotropic Polypeptide (3-42) (human)

LEPIRUDIN. 1mg Synthetic peptide. Lepirudin is an anticoagulant which functions as a direct thrombin inhibitor.

LEPIRUDIN. 5mg Synthetic peptide. Lepirudin is an anticoagulant which functions as a direct thrombin inhibitor.

VAPREOTIDE. 5mg Vapreotide is a potent octapeptide analog of somatostatin with selectivity for the somatostatin receptor subtypes SSTR-2 and SSTR-5. It is under investigation in the management of various disorders, including esophageal variceal bleeding, gastrointestinal and pancreatic fistulas, acromegaly, carcinoid tumors, and for the prevention of postoperative complications following pancreatic surgery. (Disulfide bond) CAS: 103222-11-3 C57H70N12O9S2 FW: 1131.39 . Synonym: RC-160

VAPREOTIDE. 25mg Vapreotide is a potent octapeptide analog of somatostatin with selectivity for the somatostatin receptor subtypes SSTR-2 and SSTR-5. It is under investigation in the management of various disorders, including esophageal variceal bleeding, gastrointestinal and pancreatic fistulas, acromegaly, carcinoid tumors, and for the prevention of postoperative complications following pancreatic surgery. (Disulfide bond) CAS: 103222-11-3 C57H70N12O9S2 FW: 1131.39 . Synonym: RC-160

(D-TRP3)-LEUPROLIDE. 1mg Impurity E of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42 . Synonym: (D-Trp3)-Leuprolide, (D-Trp3)-Leuprorelin

(D-TRP3)-LEUPROLIDE. 5mg Impurity E of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42 . Synonym: (D-Trp3)-Leuprolide, (D-Trp3)-Leuprorelin

(D-HIS2,D-SER4)-LEUPROLIDE, 1mg Impurity F of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42. Synonym: (D-His2,D-Ser4)-Leuprolide, (D-His2,D-Ser4)-Leuprorelin.

(D-HIS2,D-SER4)-LEUPROLIDE, 5mg Impurity F of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42. Synonym: (D-His2,D-Ser4)-Leuprolide, (D-His2,D-Ser4)-Leuprorelin.

(D-PYR1)-LEUPROLIDE. 1mg Impurity I of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42 . Synonym: (D-Pyr1)-Leuprolide, (D-Pyr1)-Leuprorelin

(D-PYR1)-LEUPROLIDE. 5mg Impurity I of the Leuprorelin Ph. Eur. monograph. C59H84N16O12 FW: 1209.42 . Synonym: (D-Pyr1)-Leuprolide, (D-Pyr1)-Leuprorelin

(SER(TBU)6,AZAGLY10)-LHRH, 1mg Impurity B of the Goserelin Ph. Eur. monograph. C59H84N18O14 FW: 1269.43. Synonym: (Ser(tBu)6)-Goserelin.

(SER(AC)4)-GOSERELIN. 1mg Impurity K of the Goserelin Ph. Eur. monograph. C61H86N18O15 FW: 1311.47 . Synonym: (Ser(Ac)4)-Goserelin

(SER(AC)4)-GOSERELIN. 5mg Impurity K of the Goserelin Ph. Eur. monograph. C61H86N18O15 FW: 1311.47 . Synonym: (Ser(Ac)4)-Goserelin

EPTIFIBATIDE. 1mg Eptifibatide, a RGD mimetic, is a glycoprotein (GP) IIb/IIIa receptor antagonist. Clinically, the peptide is used as an antiplatelet drug in combination with heparin and aspirin in the management of unstable angina and in patients undergoing coronary angioplasty and stenting procedures.

EPTIFIBATIDE. 5mg Eptifibatide, a RGD mimetic, is a glycoprotein (GP) IIb/IIIa receptor antagonist. Clinically, the peptide is used as an antiplatelet drug in combination with heparin and aspirin in the management of unstable angina and in patients undergoing coronary angioplasty and stenting procedures.

EPTIFIBATIDE. 25mg Eptifibatide, a RGD mimetic, is a glycoprotein (GP) IIb/IIIa receptor antagonist. Clinically, the peptide is used as an antiplatelet drug in combination with heparin and aspirin in the management of unstable angina and in patients undergoing coronary angioplasty and stenting procedures.

Bivalirudin, Bg 8967, Hirulog, Hirulog I, H-D-Phe-Pro-Arg-Pro-Gly-Gly-Gly-Gly-Asn-Gly-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Oh 100Mg,Trifluoroacetate salt, C98H128N24O22, Cas no: [128270-60-0] net, Bivalirudin is a highly specific and reversible direct thrombin inhibitor.

BIVALIRUDIN. 500mg Highly specific and reversible direct thrombin inhibitor.

BIOTINYL-HEPCIDIN-25 (HUMAN). 0.5mg (Disulfide bonds between Cys7 and Cys23/Cys10 and Cys13/Cys11 and Cys19/Cys14 and Cys22) C123H184N36O33S10 FW: 3015.7 . Synonym: Biotinyl-Hepc25 (human), Biotinyl-LEAP-1 (human), Biotinyl-Liver-Expressed Antimicrobial Peptide (human), Biotinyl-PLTR (human), Biotinyl-Putative Liver Tumor Regressor (human)

BIOTINYL-HEPCIDIN-25 (HUMAN). 1mg (Disulfide bonds between Cys7 and Cys23/Cys10 and Cys13/Cys11 and Cys19/Cys14 and Cys22) C123H184N36O33S10 FW: 3015.7 . Synonym: Biotinyl-Hepc25 (human), Biotinyl-LEAP-1 (human), Biotinyl-Liver-Expressed Antimicrobial Peptide (human), Biotinyl-PLTR (human), Biotinyl-Putative Liver Tumor Regressor (human)

CETRORELIX. 1mg GnRH antagonist.

CETRORELIX. 5mg GnRH antagonist.

ENFUVIRTIDE. 1mg Enfuvirtide is a 36 amino acid peptide corresponding to a region of gp41, the transmembrane subunit of HIV-1 envelope protein. It belongs to the therapeutic class of fusion inhibitors and acts by binding to gp41 and impeding the conformational changes in gp41 necessary for fusion of the virus with the cell.eeThis product is offered and sold solely for uses reasonably related to the development and submission of information under a Federal law which regulates the manufacture, use or sale of drug s (the GCBolar ExemptionGCY). Bachem cannot be made liable for any infringement of intellectual property rights. It is the sole and only responsibility of the purchaser or user of this product to comply with the relevant national rules and regulations. CAS: 159519-65-0 C204H301N51....

ENFUVIRTIDE. 5mg Enfuvirtide is a 36 amino acid peptide corresponding to a region of gp41, the transmembrane subunit of HIV-1 envelope protein. It belongs to the therapeutic class of fusion inhibitors and acts by binding to gp41 and impeding the conformational changes in gp41 necessary for fusion of the virus with the cell.eeThis product is offered and sold solely for uses reasonably related to the development and submission of information under a Federal law which regulates the manufacture, use or sale of drug s (the GCBolar ExemptionGCY). Bachem cannot be made liable for any infringement of intellectual property rights. It is the sole and only responsibility of the purchaser or user of this product to comply with the relevant national rules and regulations. CAS: 159519-65-0 C204H301N51O....

ADROPIN 34-76 (HUMAN, MOUSE, RAT), 0.5mg Adropin is a secreted factor involved in energy homeostasis and lipid metabolism. It is encoded by the energy homeostasis associated gene (Enho) and is expressed in liver and brain. In diet-induced obesity (DIO) mice Adropin (34-76) (human, mouse, rat) attenuated hepatosteatosis and insulin reistance independently of adiposity or food intake. (Disulfide bond) C190H293N55O68S2 FW: 4499.88. adropin.

ADROPIN 34-76 (HUMAN, MOUSE, RAT), 1mg Adropin is a secreted factor involved in energy homeostasis and lipid metabolism. It is encoded by the energy homeostasis associated gene (Enho) and is expressed in liver and brain. In diet-induced obesity (DIO) mice Adropin (34-76) (human, mouse, rat) attenuated hepatosteatosis and insulin reistance independently of adiposity or food intake. (Disulfide bond) C190H293N55O68S2 FW: 4499.88. adropin.

(GLY22)-AMYLOID B-PROTEIN (1-40). 0.5mg The highly neurotoxic arctic mutant (E22G) of A+ has been used to study the mechanisms underlying the formation of soluble and insoluble +-amyloid aggregates. As the wild-type A+, the arctic mutant preferably assembles in the presence of GM1 ganglioside. CAS: 175010-18-1 C191H291N53O56S FW: 4257.8 . Synonym: Amyloid b-Protein (1-40) Arctic Mutation, Amyloid b-Protein (1-40) E22G

(GLY22)-AMYLOID B-PROTEIN (1-40). 1mg The highly neurotoxic arctic mutant (E22G) of A+ has been used to study the mechanisms underlying the formation of soluble and insoluble +-amyloid aggregates. As the wild-type A+, the arctic mutant preferably assembles in the presence of GM1 ganglioside. CAS: 175010-18-1 C191H291N53O56S FW: 4257.8 . Synonym: Amyloid b-Protein (1-40) Arctic Mutation, Amyloid b-Protein (1-40) E22G

(GLN22)-AMYLOID B-PROTEIN (1-40). 0.5mg The Dutch mutation (E22Q) of amyloid +-peptide aggegates more readily than the wild-type peptide and the resulting fibrils show increased neurotoxicity. The mutant peptide E22Q induced apoptosis of cerebral endothelial cells at a concentration of 25 ++m, whereas WT A+ 1-40 and the Italian mutant E22K (H-6698) showed no effect. CAS: 144410-00-4 C194H296N54O57S FW: 4328.88 . Synonym: Amyloid b-Protein (1-40) Dutch Mutation, Amyloid b-Protein (1-40) E22Q

(GLN22)-AMYLOID B-PROTEIN (1-40). 1mg The Dutch mutation (E22Q) of amyloid +-peptide aggegates more readily than the wild-type peptide and the resulting fibrils show increased neurotoxicity. The mutant peptide E22Q induced apoptosis of cerebral endothelial cells at a concentration of 25 ++m, whereas WT A+ 1-40 and the Italian mutant E22K (H-6698) showed no effect. CAS: 144410-00-4 C194H296N54O57S FW: 4328.88 . Synonym: Amyloid b-Protein (1-40) Dutch Mutation, Amyloid b-Protein (1-40) E22Q

(LYS22)-AMYLOID B-PROTEIN (1-40). 0.5mg The Italian mutation of +-amyloid 1-40 (E22K) aggregates more rapidly than the wild-type sequence 1-40. It showed increased neurotoxicity, which (according to a solid-phase NMR-study of Masuda et al.) may be due to the salt bridge formed between Lys-- and Asp-- in the minor conformer. As the Arctic, Flemish, and Dutch mutants, the Italian mutant is degraded considerably more slowly than wild-type A+ by neprilysin. CAS: 302905-01-7 C195H300N54O56S FW: 4328.92 . Synonym: Amyloid b-Protein (1-40) Italian Mutation, Amyloid b-Protein (1-40) E22K

(LYS22)-AMYLOID B-PROTEIN (1-40). 1mg The Italian mutation of +-amyloid 1-40 (E22K) aggregates more rapidly than the wild-type sequence 1-40. It showed increased neurotoxicity, which (according to a solid-phase NMR-study of Masuda et al.) may be due to the salt bridge formed between Lys-- and Asp-- in the minor conformer. As the Arctic, Flemish, and Dutch mutants, the Italian mutant is degraded considerably more slowly than wild-type A+ by neprilysin. CAS: 302905-01-7 C195H300N54O56S FW: 4328.92 . Synonym: Amyloid b-Protein (1-40) Italian Mutation, Amyloid b-Protein (1-40) E22K

(DES-SER4)-LEUPROLIDE. 1mg CAS: 267878-61-5 C56H79N15O10 FW: 1122.34 . Synonym: (Des-Ser4)-Leuprolide, (Des-Ser4)-Leuprorelin

(DES-SER4)-LEUPROLIDE. 5mg CAS: 267878-61-5 C56H79N15O10 FW: 1122.34 . Synonym: (Des-Ser4)-Leuprolide, (Des-Ser4)-Leuprorelin

(ORN8)-LEUPROLIDE. 1mg CAS: 1051970-61-6 C58H82N14O12 FW: 1167.38 . Synonym: (Orn8)-Leuprolide, (Orn8)-Leuprorelin

(ORN8)-LEUPROLIDE. 5mg CAS: 1051970-61-6 C58H82N14O12 FW: 1167.38 . Synonym: (Orn8)-Leuprolide, (Orn8)-Leuprorelin

COPEPTIN (HUMAN). 0.5mg Copeptin is initially produced in equimolar amounts to (ArgG+)-Vasopressin (AVP). Due to the high stability of copeptin in plasma and serum its measurement is not affected by the problems, which are associated with the direct measurement of AVP, and thus, is suitable to indirectly determine the release of AVP. Copeptin has emerged as a prognostic marker in a variety of diseases, such as sepsis, community-acquired pneumonia, chronic obstructive pulmonary failure, heart failure and myocardial infarction. CAS: 78362-34-2 C177H279N49O58 FW: 4021.46 . copeptin

COPEPTIN (HUMAN). 1mg Copeptin is initially produced in equimolar amounts to (ArgG+)-Vasopressin (AVP). Due to the high stability of copeptin in plasma and serum its measurement is not affected by the problems, which are associated with the direct measurement of AVP, and thus, is suitable to indirectly determine the release of AVP. Copeptin has emerged as a prognostic marker in a variety of diseases, such as sepsis, community-acquired pneumonia, chronic obstructive pulmonary failure, heart failure and myocardial infarction. CAS: 78362-34-2 C177H279N49O58 FW: 4021.46 . copeptin

ATOSIBAN. 50mg Oxytocin/vasopressin receptor antagonist. (Disulfide bond) CAS: 90779-69-4 C43H67N11O12S2 FW: 994.2 . Synonym: Atosiban, RWJ 22164

ATOSIBAN. 250mg Oxytocin/vasopressin receptor antagonist. (Disulfide bond) CAS: 90779-69-4 C43H67N11O12S2 FW: 994.2 . Synonym: Atosiban, RWJ 22164

ATOSIBAN. 1G Oxytocin/vasopressin receptor antagonist. (Disulfide bond) CAS: 90779-69-4 C43H67N11O12S2 FW: 994.2 . Synonym: Atosiban, RWJ 22164

COPEPTIN (RAT). 0.5mg CAS: 86280-64-0 C183H307N57O61 FW: 4281.8 . copeptin

COPEPTIN (RAT). 1mg CAS: 86280-64-0 C183H307N57O61 FW: 4281.8 . copeptin

LHRH. 5mg CAS: 33515-09-2 C55H75N17O13 FW: 1182.31 . Synonym: Gonadorelin, GnRH, Luliberin

LHRH. 25mg CAS: 33515-09-2 C55H75N17O13 FW: 1182.31 . Synonym: Gonadorelin, GnRH, Luliberin

MAXADILAN. 0.5mg Maxadilan, isolated from the salivary gland of the sand fly Lutzomyia longipalpis, is a potent vasodilator. The peptide specifically and potently activates the mammalian PAC1 receptor, one of the three receptors for PACAP. (Disulfide bonds between Cys1 and Cys5/Cys14 and Cys51) CAS: 135374-80-0 C291H466N86O94S6 FW: 6865.82 . maxadilan

MAXADILAN. 1mg Maxadilan, isolated from the salivary gland of the sand fly Lutzomyia longipalpis, is a potent vasodilator. The peptide specifically and potently activates the mammalian PAC1 receptor, one of the three receptors for PACAP. (Disulfide bonds between Cys1 and Cys5/Cys14 and Cys51) CAS: 135374-80-0 C291H466N86O94S6 FW: 6865.82 . maxadilan

M65. 0.5mg Potent and specific PAC1 receptor antagonist. (Disulfide bonds between Cys1 and Cys5/Cys14 and Cys32) C199H314N62O60S5 FW: 4695.39 . Synonym: PAC1 Receptor Antagonist M65

M65. 1mg Potent and specific PAC1 receptor antagonist. (Disulfide bonds between Cys1 and Cys5/Cys14 and Cys32) C199H314N62O60S5 FW: 4695.39 . Synonym: PAC1 Receptor Antagonist M65

ACTH (2-24) (human, bovine, rat) 1mg. ACTH (2-24) (human, bovine, rat) H-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Molecular Formula: CGGGHGGGNGGOGGS, Cas number: 67654-32-4.

ACTH (2-24) (human, bovine, rat) 5mg. ACTH (2-24) (human, bovine, rat) H-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 5mg, Molecular Formula: CGGGHGGGNGGOGGS, Cas number: 67654-32-4.

(Des-Ser3)-ACTH (1-24) (human, bovine, rat) 1mg. (Des-Ser3)-ACTH (1-24) (human, bovine, rat), H-Ser-Tyr-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH, Trifluoroacetate salt 1mg, Molecular Formula: CGGGHGGGNGGOGGS.

(Des-Ser3)-ACTH (1-24) (human, bovine, rat) 5mg. (Des-Ser3)-ACTH (1-24) (human, bovine, rat), H-Ser-Tyr-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH, Trifluoroacetate salt 5mg, Molecular Formula: CGGGHGGGNGGOGGS.

Acetyl-ACTH (3-24) (human, bovine, rat) 1mg. Acetyl-ACTH (3-24) (human, bovine, rat), Ac-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt, 1mg, Molecular Formula: CGGGHGGGNGGOGGS, Source: Synthetic.

Acetyl-ACTH (3-24) (human, bovine, rat) 5mg. Acetyl-ACTH (3-24) (human, bovine, rat), Ac-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt, 5 mg, Molecular Formula: CGGGHGGGNGGOGGS, Source: Synthetic.

Acetyl-ACTH (2-24) (human, bovine, rat) 1mg. Acetyl-ACTH (2-24) (human, bovine, rat) Ac-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Synonym: Acetyl-Tetracosactide (2-24), Molecular Formula: CGGGHGGGNGGOGGS.

Acetyl-ACTH (2-24) (human, bovine, rat) 5mg. Acetyl-ACTH (2-24) (human, bovine, rat) Ac-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 5mg, Synonym: Acetyl-Tetracosactide (2-24), Molecular Formula: CGGGHGGGNGGOGGS.

Acetyl-ACTH (4-24) (human, bovine, rat) 1mg. Acetyl-ACTH (4-24) (human, bovine, rat), Ac-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Synonym: Acetyl-Tetracosactide (4-24), Molecular Formula: CGGGHGGGNGGOGGS.

Acetyl-ACTH (7-24) (human, bovine, rat) 1mg. Acetyl-ACTH (7-24) (human, bovine, rat) Ac-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH, Trifluoroacetate salt, 1mg, Synonyms Acetyl-Tetracosactide (7-24), Molecular Formula: CGGGHGGGNGGOGG.

Acetyl-ACTH (7-24) (human, bovine, rat) 5mg. Acetyl-ACTH (7-24) (human, bovine, rat) Ac-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH, Trifluoroacetate salt, 5mg, Synonyms Acetyl-Tetracosactide (7-24), Molecular Formula: CGGGHGGGNGGOGG.

(Des-HisG)-ACTH (1-24) (human, bovine, rat) 1mg. (Des-HisG)-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-Glu-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Synonym: (Des-HisG)-Tetracosactide, Molecular Formula: CGGGHGGGNGGOGGS.

(Des-HisG)-ACTH (1-24) (human, bovine, rat) 5mg. (Des-HisG)-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-Glu-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 5mg, Synonym: (Des-HisG)-Tetracosactide, Molecular Formula: CGGGHGGGNGGOGGS.

(Des-GluG)-ACTH (1-24) (human, bovine, rat) 1mg. (Des-GluG)-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Synonym: (Des-GluG)-Tetracosactide, Molecular Formula: CGGGHGGGNGGOGGS.

(Des-GluG)-ACTH (1-24) (human, bovine, rat) 5mg. (Des-GluG)-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 5mg, Synonym: (Des-GluG)-Tetracosactide, Molecular Formula: CGGGHGGGNGGOGGS.

Endo-4a-Glu-ACTH (1-24) (human, bovine, rat) 1mg. Endo-4a-Glu-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-Glu-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 1mg, Synonym: Endo-4a-Glu-Tetracosactide.

Endo-4a-Glu-ACTH (1-24) (human, bovine, rat) 5mg. Endo-4a-Glu-ACTH (1-24) (human, bovine, rat) H-Ser-Tyr-Ser-Met-Glu-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-OH Trifluoroacetate salt 5mg, Synonym: Endo-4a-Glu-Tetracosactide.

RELAXIN H2 (HUMAN). 1mg Relaxin H2 is the major stored and circulating isoform of the peptide hormone relaxin in humans. This pregnancy hormone has also shown cardioprotective activity. The observed long-term effects of relaxin H2 on connective tissues may be due to alterations in the turnover of collagen and proteoglycans. (Disulfide bonds between Cys10A and Cys15A/Cys11A and Cys11B/Cys24A and Cys23B) CAS: 99489-94-8 C256H408N74O74S8 FW: 5963.04 . relaxin

GLUCAGON (1-29) (HUMAN, RAT, PORCINE) 1mg Glucagon is a 29 amino acid containing peptide hormone processed from proglucagon. As a counterregulatory hormone for insulin, glucagon plays a critical role in maintaining glucose homeostasis in vivo in both animals and humans. Not surprisingly, glucagon and glucagon receptor have been pursued extensively as potential targets for the therapeutic treatment of diabetes. As Apeptides and IAPP, glucacon tends to form gel-like fibrillar aggregates. These fibrils were found to be toxic throug h the activation of apoptotic signaling pathways. Hence the aggregation behavior of glucagon has been studied extensively. CAS: 16941-32-5 C153H225N43O49S FW: 3482.8. glucagon.

GLUCAGON (1-29) (HUMAN, RAT, PORCINE) 5mg Glucagon is a 29 amino acid containing peptide hormone processed from proglucagon. As a counterregulatory hormone for insulin, glucagon plays a critical role in maintaining glucose homeostasis in vivo in both animals and humans. Not surprisingly, glucagon and glucagon receptor have been pursued extensively as potential targets for the therapeutic treatment of diabetes. As Apeptides and IAPP, glucacon tends to form gel-like fibrillar aggregates. These fibrils were found to be toxic throug h the activation of apoptotic signaling pathways. Hence the aggregation behavior of glucagon has been studied extensively. CAS: 16941-32-5 C153H225N43O49S FW: 3482.8. glucagon.

THYMOSIN A1. 1mg Thymosin +G, originally isolated from calf thymus, acts as an immunomodulator. Additionally, the peptide showed antiviral, angiogenic, and wound-healing activities.eThymosin +G was shown to activate tumor-associated macrophages. CAS: 62304-98-7 C129H215N33O55 FW: 3108.32 . Synonym: Thymalfasin

THYMOSIN A1. 5mg Thymosin +G, originally isolated from calf thymus, acts as an immunomodulator. Additionally, the peptide showed antiviral, angiogenic, and wound-healing activities.eThymosin +G was shown to activate tumor-associated macrophages. CAS: 62304-98-7 C129H215N33O55 FW: 3108.32 . Synonym: Thymalfasin

ENDOTHELIN-1 (HUMAN, BOVINE, DOG) 1mg This 21-amino acid peptide from vascular endothelial cells of different mammalian species is one of the most potent vasoconstrictors. ET-1 exerts a wide variety of effects on both vascular and non-vascular (e.g. heart, lung, brain) tissues. Toxic peptides from a snake venom, the sarafotoxins, show structural and functional homology to ET-1. The role of ET-1in clinical hypertension has been reviewed by Dhaun et al. and by Sreenivas and Oparil..

ENDOTHELIN-1 (HUMAN, BOVINE, DOG) 5mg This 21-amino acid peptide from vascular endothelial cells of different mammalian species is one of the most potent vasoconstrictors. ET-1 exerts a wide variety of effects on both vascular and non-vascular (e.g. heart, lung, brain) tissues. Toxic peptides from a snake venom, the sarafotoxins, show structural and functional homology to ET-1. The role of ET-1in clinical hypertension has been reviewed by Dhaun et al. and by Sreenivas and Oparil..

Cyclo(-Arg-Gly-Asp-D-Phe-Cys) 1mg. Cyclo(-Arg-Gly-Asp-D-Phe-Cys) Acetate salt 1mg, Synonym: c(RGDfC), avb3 Integrin Binding Cyclic RGD Peptide, Molecular Formula: CGGHGGNGOGS, Cas Number: 862772-11-0, Storage Condition: -20 +/- 5 degree C.

Cyclo(-Arg-Gly-Asp-D-Phe-Cys) 5mg. Cyclo(-Arg-Gly-Asp-D-Phe-Cys) Acetate salt 5mg, Synonym: c(RGDfC), avb3 Integrin Binding Cyclic RGD Peptide, Molecular Formula: CGGHGGNGOGS, Cas Number: 862772-11-0, Storage Condition: -20 +/- 5 degree C.

REC TNF-A (HUMAN). 50ug This monocyte-macrophage-derived cytokine was first characterized by its in vivo antitumor properties and in vitro cytotoxicity to certain transformed cell lines. TNF-+ also exerts a growth-enhancing effect on various cells and thus is a bifunctional growth regulator like e.g. IFN-+. As a mediator of inflammatory processes, TNF-+ shares many similar biological activities with IL-1. For our monoclonal antibody to rec TNF-+ (human) please see T-1401. CAS: 94948-59-1 FW: . TNF

DEFENSIN HNP-3 (HUMAN). 0.5mg (Disulfide bonds between Cys2 and Cys30/Cys4 and Cys19/Cys9 and Cys29) CAS: 136661-76-2 C151H222N44O40S6 FW: 3486.09 . Synonym: Human Neutrophil Peptide-3, HNP-3

DEFENSIN HNP-3 (HUMAN). 1mg (Disulfide bonds between Cys2 and Cys30/Cys4 and Cys19/Cys9 and Cys29) CAS: 136661-76-2 C151H222N44O40S6 FW: 3486.09 . Synonym: Human Neutrophil Peptide-3, HNP-3

Bz-Phe-Val-Arg-AMC.

Bz-Phe-Val-Arg-AMC.

Glutaryl-Gly-Arg-AMC.