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Cat. No.
Name
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RP13084
Orphanin FQ/Nociceptin, human, mouse, ox, rat
0.500 mg
$90
Orphanin FQ/Nociceptin, Human, Mouse, Ox, Rat

Full Name Orphanin FQ/Nociceptin, Human, Mouse, Ox, Rat
Alias
Orphanin FQ,human, mouse, ox, rat
Documents
Document-HPLC: 2174_20060721145624.PDF (PDF)
Document-MS: 1927_20060721145603.PDF (PDF)
Document-MSDS: 5418_20080820223347.PDF (PDF)
TECHNICAL MANUAL: 12464_20100407015038.PDF (PDF)
Figures
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Reference
Sequence
(one-letter code)
FGGFTGARKSARKLANQ
Sequence
(three-letter code)
{PHE}{GLY}{GLY}{PHE}{THR}{GLY}{ALA}{ARG}{LYS}{SER}{ALA}{ARG}{LYS}{LEU}{ALA}{ASN}{GLN}
Description
Orphanin FQ was identified and purified from porcine brain tissue as a ligand for an orphan heterotrimeric GTP-inding protein (G protein)-coupled receptor (LC132) that is similar in sequence to opioid receptors. Orphanin FQ has a primary structure reminiscent of that of opioid peptides. Nanomolar concentrations of orphanin FQ have inhibited forskolin-stimulated adenylyl cyclase activity in cells transfected with LC132. This inhibitory activity was not affected by the addition of opioid ligands, nor did the peptide activate opioid receptors. Orphanin FQ bound to its receptor in a saturable manner and with high affinity.
Solubility
The peptide is 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
Storage at -20°C. Keep tightly closed.
Notes
In conscious rats intravenous infusion of orphanin FQ produced a profound increase in urine flow rate and decrease in urinary sodium excretion.
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