OPRM1
Reaktivität: Human
WB, ELISA
Wirt: Maus
Polyclonal
unconjugated
Applikationshinweise
ELISA: 1: 20000approx. 1: 40000. WB: 1: 500approx. 1: 1000. IHC: 1: 50approx. 1: 200. Other applications not tested. Optimal dilutions are dependent on conditions and should be determined by the user.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Konzentration
1.0 mg/mL
Buffer
Phosphate buffered saline (PBS), pH ~7.2, 15 mM Sodium Azide
Konservierungsmittel
Sodium azide
Vorsichtsmaßnahmen
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handhabung
Avoid repeated freezing and thawing.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target
Mu Opioid Receptor 1 (OPRM1)
(Opioid Receptor, mu 1 (OPRM1))
LMOR antikoerper, M-OR-1 antikoerper, MOP antikoerper, MOR antikoerper, MOR1 antikoerper, OPRM antikoerper, MOP-R antikoerper, MOR-1 antikoerper, MOR-1O antikoerper, Oprm antikoerper, mor antikoerper, muOR antikoerper, MORA antikoerper, Oprrm1 antikoerper, or2 antikoerper, ZFOR2 antikoerper, OPRM1 antikoerper, opioid receptor mu 1 antikoerper, opioid receptor, mu 1 antikoerper, outer membrane protein OprM antikoerper, OPRM1 antikoerper, Oprm1 antikoerper, oprm1 antikoerper, oprM1 antikoerper
Hintergrund
Three types of opioid receptors have been cloned: mu, delta, and kappa. Opioid receptors 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 μ-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.Synonyms: MOR1, Mu-type opioid receptor