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A-CGRP (8-37) (MOUSE, RAT), 5mg It has been demonstrated that this competitive CGRP1 receptor antagonist exhibited hypothermic and antinociceptive effects. This peptide antagonized the effects of amylin and amylin (1-8) on osteoblasts but was substantially less potent in this regard than amylin (8-37) (H-2746). Furthermore, it inhibited the evoked discharge frequency of wide dynamic range neurons in dorsal horn of the spinal cord in rats. CAS: 129121-73-9 C138H224N42O41 FW: 3127.56. Synonym: Calcitonin Gene-Related Peptide I (8-37) (mouse, rat), CGRP-I (8-37) (mouse, rat)

Description: A-CGRP (8-37) (MOUSE, RAT), 5mg It has been demonstrated that this competitive CGRP1 receptor antagonist exhibited hypothermic and antinociceptive effects. This peptide antagonized the effects of amylin and amylin (1-8) on osteoblasts but was substantially less potent in this regard than amylin (8-37) (H-2746). Furthermore, it inhibited the evoked discharge frequency of wide dynamic range neurons in dorsal horn of the spinal cord in rats. CAS: 129121-73-9 C138H224N42O41 FW: 3127.56. Synonym: Calcitonin Gene-Related Peptide I (8-37) (mouse, rat), CGRP-I (8-37) (mouse, rat)
Catalog Number: H-4924.0005BA
Supplier: Bachem Americas
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PEPTIDE YY (3-36) (HUMAN)

Description: 1mg PYY (3-36), a Y2 receptor agonist, is released from the body's gastrointestinal tract in proportion to caloric intake. It has been shown that peripheral injection of PYY (3-36) in rats inhibited food intake and reduced weight gain. In addition, infusion of PYY (3-36) in humans significantly decreased appetite and reduced food intake by 33% over 24h, which sug gests that PYY (3-36) has a role in 'longer term' regulation of food intake. Thus, the PYY (3-36) may represent a lead compound for the development of drug s for the treatment of obesity. CAS: 123583-37-9 C180H279N53O54 FW: 4049.52 . Synonym: PYY (3-36) (human)
Catalog Number: H-8585.1000BA
Supplier: Bachem Americas
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PEPTIDE YY (3-36) (HUMAN)

Description: 0.5mg PYY (3-36), a Y2 receptor agonist, is released from the body's gastrointestinal tract in proportion to caloric intake. It has been shown that peripheral injection of PYY (3-36) in rats inhibited food intake and reduced weight gain. In addition, infusion of PYY (3-36) in humans significantly decreased appetite and reduced food intake by 33% over 24h, which sug gests that PYY (3-36) has a role in 'longer term' regulation of food intake. Thus, the PYY (3-36) may represent a lead compound for the development of drug s for the treatment of obesity. CAS: 123583-37-9 C180H279N53O54 FW: 4049.52 . Synonym: PYY (3-36) (human)
Catalog Number: H-8585.0500BA
Supplier: Bachem Americas
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AC-YVAD-CHO

Description: 25mg Ac-YVAD-CHO is a potent, specific, reversible inhibitor of caspase-1 (ICE). It displayed a Ki of 0.2 ± 0.1 nM for recombinant human caspase-1. CAS: 143313-51-3 C23H32N4O8 FW: 492.53 . Synonym: Ac-YVAD-CHO, L-709049
Catalog Number: H-8410.0025BA
Supplier: Bachem Americas
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AC-YVAD-CHO

Description: 5mg Ac-YVAD-CHO is a potent, specific, reversible inhibitor of caspase-1 (ICE). It displayed a Ki of 0.2 ± 0.1 nM for recombinant human caspase-1. CAS: 143313-51-3 C23H32N4O8 FW: 492.53 . Synonym: Ac-YVAD-CHO, L-709049
Catalog Number: H-8410.0005BA
Supplier: Bachem Americas
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SV40 NUCLEAR TRANSPORT SIGNAL PEP

Description: 1mg This peptide, containing 7 amino acids homologous to the SV40 T antigen, was capable of inducing the transport of several carrier proteins to the nucleus. The terminal cysteine permits the attachment of this peptide to any protein using a heterobifunctional crosslinking reagent. Coupling to plasmid DNA has also been realized by M.G.Sebastyén and coworkers. CAS: 104914-40-1 C60H104N20O15S FW: 1377.68 . SV40
Catalog Number: H-8120.0001BA
Supplier: Bachem Americas
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ACETYL-HIRUDIN (53-65) (SULFATED)

Description: 1mg Hirug en, the C-terminal fragment of hirudin (residues 53-65) binds to and thereby protects thrombin against cleavage by trypsin, and to a lesser degree prevents the cleavage of thrombin by pancreatic elastase. CAS: 348603-19-0 C72H100N14O32S FW: 1705.73 . Synonym: Hirug en
Catalog Number: H-8190.0001BA
Supplier: Bachem Americas
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SV40 NUCLEAR TRANSPORT SIGNAL PEP

Description: 5mg This peptide, containing 7 amino acids homologous to the SV40 T antigen, was capable of inducing the transport of several carrier proteins to the nucleus. The terminal cysteine permits the attachment of this peptide to any protein using a heterobifunctional crosslinking reagent. Coupling to plasmid DNA has also been realized by M.G.Sebastyén and coworkers. CAS: 104914-40-1 C60H104N20O15S FW: 1377.68 . SV40
Catalog Number: H-8120.0005BA
Supplier: Bachem Americas
Image Unavailable-H-8735.0500BA

EXENDIN-3

Description: 0.5mg Exendin-3, a member of the glucagon superfamily, was originally isolated from the venom of the lizard, Heloderma horridum. At low concentrations, the 39-amino acid peptide interacts with putative exendin receptors causing an increase in pancreatic acinar cAMP, whereas at higher concentrations it interacts with VIP receptors to stimulate an increase in cellular cAMP and amylase release. CAS: 130357-25-4 C184H282N50O61S FW: 4202.63 . exendin
Catalog Number: H-8735.0500BA
Supplier: Bachem Americas
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EXENDIN (9-39)

Description: 1mg Exendin (9-39) is a potent glucagon-like peptide 1 (GLP-1) receptor antagonist. It has also been described as an antagonist of the putative exendin receptor. This peptide blocks the stimulatory action of GLP-1 (7- 36) amide (H- 6795) and of exendin-4 (H- 8730) on cAMP production in pancreatic acini. - Moreover, exendin (9-39) was shown to be safely used to abolish the incretin effect of GLP-1 without interfering with the control of insulin secretion by circulating nutrients. CAS: 133514-43-9 C149H234N40O47S FW: 3369.8 . exendin
Catalog Number: H-8740.1000BA
Supplier: Bachem Americas
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EXENDIN (9-39)

Description: 0.5mg Exendin (9-39) is a potent glucagon-like peptide 1 (GLP-1) receptor antagonist. It has also been described as an antagonist of the putative exendin receptor. This peptide blocks the stimulatory action of GLP-1 (7- 36) amide (H- 6795) and of exendin-4 (H- 8730) on cAMP production in pancreatic acini. - Moreover, exendin (9-39) was shown to be safely used to abolish the incretin effect of GLP-1 without interfering with the control of insulin secretion by circulating nutrients. CAS: 133514-43-9 C149H234N40O47S FW: 3369.8 . exendin
Catalog Number: H-8740.0500BA
Supplier: Bachem Americas
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(D-TRP12,TYR34)-PTH (7-34) AMIDE, 1mg The D-Trp12 substitution leads to a competitive pTH antagonist with increased inhibitory properties in vitro. CAS: 118102-98-0 C165H251N49O40S2 FW: 3625.25. pTH

Description: (D-TRP12,TYR34)-PTH (7-34) AMIDE, 1mg The D-Trp12 substitution leads to a competitive pTH antagonist with increased inhibitory properties in vitro. CAS: 118102-98-0 C165H251N49O40S2 FW: 3625.25. pTH
Catalog Number: H-9115.1000BA
Supplier: Bachem Americas
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(D-TRP12,TYR34)-PTH (7-34) AMIDE, 0.5mg The D-Trp12 substitution leads to a competitive pTH antagonist with increased inhibitory properties in vitro. CAS: 118102-98-0 C165H251N49O40S2 FW: 3625.25. pTH

Description: (D-TRP12,TYR34)-PTH (7-34) AMIDE, 0.5mg The D-Trp12 substitution leads to a competitive pTH antagonist with increased inhibitory properties in vitro. CAS: 118102-98-0 C165H251N49O40S2 FW: 3625.25. pTH
Catalog Number: H-9115.0500BA
Supplier: Bachem Americas
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H-DL-ALA-DL-ALA-OH

Description: 5G CAS: 2867-20-1 C6H12N2O3 FW: 160.17
Catalog Number: G-1140.0005BA
Supplier: Bachem Americas
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H-DL-ALA-DL-ALA-OH

Description: 25G CAS: 2867-20-1 C6H12N2O3 FW: 160.17
Catalog Number: G-1140.0025BA
Supplier: Bachem Americas
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H-ALA-GLN-OH

Description: 5G The dipeptides H-Ala-Gln-OH and H-Gly-Gln-OH (N-1070) are stable substitutes for Gln in cell culture media, which tolerate autoclaving and liberate a lower amount of undesired ammonia than Gln. Ala-Gln and Gly-Gln have also found use as Gln sources in parenteral nutrition. CAS: 39537-23-0 C8H15N3O4 FW: 217.23
Catalog Number: G-1210.0005BA
Supplier: Bachem Americas
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