MOR-1 (N369) Peptide

Cat no: BS1263P

Supplier: Bioworld Technology, Inc.

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Three types of opioid receptors have been cloned: mu, delta, and kappa. Opioid eceptors are seven transmembrane G-protein coupled receptors. They share a high degree of homology and are most divergent at the N- and C-termini. Activation of mu opioid receptors leads to a decrease in neuronal excitability. Most actions of exogenous opioids, such as morphine, are mediated through the micro-opioid receptor, including analgesia, tolerance and reward. In general, opioids modulate numerous central and peripheral processes including pain perception, neuroendocrine secretion and the immune response. The opioid signal is transduced from receptors through G proteins to various different effectors. Subsequent to G protein activation, several effectors are known to orchestrate the opioid signal. For example, activation of opioid receptors increases phosphatidylinositol turnover, activates K+ channels and reduces adenylyl cyclase and Ca++ channel activities.

Catalogue number:	BS1263P
Applications:	Block/Neutralize/Inhibit
Swiss prot:	P35372
Form:	1 mg/ml in DI water.
Purity:	Synthetic peptide MOR-1 (N369). (Note: the amino acid sequence is proprietary). The purity is > 98%.
Storage temp:	Store at 4 degree C short term. Aliquot and store at -20 degree C long term. Avoid freeze-thaw cycles.
Alternative names:	Mu-type opioid receptor; M-OR-1; MOR-1; Mu opiate receptor; Mu opioid receptor; MOP; hMOP; OPRM1; MOR1
Additional info:	This peptide can be used with studies using BS1263 MOR-1 (N369) pAb.

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MOR-1 (N369) Peptide

Cat no: BS1263P

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