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Cat. No.
Name
Size   
Price
Selected
RP10338-0.5
PACAP (6-38), human, ovine, rat
0.500 mg
$133
RP10338-5
PACAP (6-38), human, ovine, rat
5 mg
$950
PACAP (6-38), Human, Ovine, Rat

Full Name PACAP (6-38), Human, Ovine, Rat
Sequence
(one-letter code)
FTDSYSRYRKQMAVKKYLAAVLGKRYKQRVKNK-NH2
Documents
Document-HPLC: 1989_20060721145615.PDF (PDF)
Document-MS: 1742_20060721145555.PDF (PDF)
Document-DATASHEET: 3788_20080130215549.DOC (DOC)
TECHNICAL MANUAL: 12464_20100407015038.PDF (PDF)
Figures
Reference
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-Terminal
NH2
Description
PACAP (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.
Solubility
Soluble 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.
Purity
> 95%
Storage
Store the peptide at -20°C.
Notes
This peptide is a potent agonist.
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