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PACAP (6-38), human, ovine, rat

Cat. No. Size Price Figures
RP10338-0.5 mg
0.5 mg
$ 133.00
HPLC:  20060721145615  (PDF)
MS:  20060721145555  (PDF)
DATASHEET:  20080130215549  (DOC)
PROTOCOL:  20100407015038  (PDF)


References:
  • Lenard L Jr, et al. Inhibitory effect of PACAP(6-38) on relaxations induced by PACAP, VIP and non-adrenergic, non-cholinergic nerve stimulation in the guinea-pig taenia caeci. Naunyn Schmiedebergs Arch. Pharmacol. May 2000; 361(5): 492-497.
  • Filipsson K, et al. PACAP contributes to insulin secretion after gastric glucose gavage in mice. Am. J. Physiol. Regul. Integr. Comp. Physiol. Aug 2000; 279(2): R424-432.
RP10338-5 mg
5 mg
$ 950.00
Full Name
PACAP (6-38), human, ovine, rat
Sequence
(one-letter code)
FTDSYSRYRKQMAVKKYLAAVLGKRYKQRVKNK-NH2
Sequence
(three-letter code)
{PHE}{THR}{ASP}{SER}{TYR}{SER}{ARG}{TYR}{ARG}{LYS}
{GLN}{MET}{ALA}{VAL}{LYS}{LYS}{TYR}{LEU}{ALA}{ALA}
{VAL}{LEU}{GLY}{LYS}{ARG}{TYR}{LYS}{GLN}{ARG}{VAL}
{LYS}{ASN}{LYS}-NH2
C-TerminalNH2
DescriptionPACAP (6-38) is a potent antagonist of PACAP 38. PACAP (6-38) is much more potent and selective than PACAP (6-27) in the inhibition of PACAP-27-stimulated pituitary adenylate cyclase. Ki values for the inhibition of the enzyme were 7nM and 150 nM, respectively. PACAP (6-38) caused a small but significant (approximately 20%) inhibition of the NANC relaxation due to electrical field stimulation (1 Hz or 10 Hz for 20 s). At these frequencies PACAP (6-38) caused no inhibition of the NANC relaxation in the presence of the P2 purinoceptor antagonist pyridoxal-phosphate-6-azophenyl-2',4'-disulphonic acid (or PPADS) plus the NO-synthase blocker NG-nitro-L-arginine; in preparations pretreated with L-NOARG alone, PACAP (6-38) retained its inhibitory effect.
SolubilitySoluble in water. The contents of this vial have been accurately determined. Both the stopper and the vial have been siliconized. Do not attempt to weigh out a smaller portion of the contents.
FormulaC182H300N56O45S1
M.W.4024.76
Purity> 95%
StorageStore the peptide at -20°C.
NotesThis peptide is a potent agonist.
* For Non-Clinical Research Use Only *
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