Opioid Receptor, mu, CT, aa391-398
Catalog No : USB-O7030-37P
467.83€
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| Product name | Opioid Receptor, mu, CT, aa391-398 | ||
|---|---|---|---|
| Catalog No | USB-O7030-37P | ||
| Supplier’s Catalog No | O7030-37P | ||
| Supplier | US Biologicals | ||
| Source antigen | Synthetic peptide | ||
| Reactivity | |||
| Cross reactivity | |||
| Applications | |||
| Molecular weight | 930.1 | ||
| Storage | 4°C | ||
|---|---|---|---|
| Other names | |||
| Grade | Purified | ||
| Purity | ≥ 95% (HPLC) | ||
| Form | Lyophilized. Reconstitute initially in a small volume of 25% acetonitrile in water or 25% ethanol in water to make a concentrated stock solution and dilute aqueous buffer. | ||
| Reactivity life | 12 months | ||
| Note | For reserch purpose only | ||
| Purity | ≥ 95% (HPLC) | ||
| Description | The function of the delta-opioid receptors has not been determined. However, recent studies in rodents have linked delta-opioid receptor antagonists with prevention of morphine tolerance and dependence without relinquishing mu-opioid antinociception. 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. Amino Acid Sequence (391-398): NH2-CGAGTAPLP-COOH Molecular Weight: 930.1 Control Peptide for Opioid Receptor, mu, CT, aa391-398 Pab Rb x Hu O7030-37. | ||
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