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μ-Opioidreceptor(extracellular)(rat),pAb正品原装

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BML-SA649-0200 200 µl
BML-SA649-0050 50 µl  
 
Endogenous opiates such as endorphins, endomorphins, and enkephalins, as well as opiate drugs (including morphine) exert their effects by binding to opioid receptors. Three "classic" types of opioid receptors have been identified: Mu (µ)-opioid (MOP) receptor, delta (δ)-opioid (DOP) receptor, and κ (κ)-opioid (KOP) receptor1. The opioid receptors belong to the G protein-coupled receptor superfamily. All three classic opioid receptors mediate opioid-induced analgesia.
Supraspinal analgesia is mainly mediated by the µ-opioid receptor, whereas µ-, δ-, and κ-receptors participate in the control of pain at the spinal level2. The opioid receptors also mediate the mood-altering properties of opioids2. Of the opioid receptors, the µ-opioid receptor has been the most extensively studied due to its important role in mediating the actions of morphine and other analgesic agents, as well as other addictive drugs such as heroin1. The µ-opioid receptors are expressed in the central nervous system and in the peripherial nervous system3. The highest densities are found in the thalamus, caudate putamen, neocortex, amygdala, and other brain regions known to have well established roles in pain and analgesia4.
Product Specification
Alternative Name: MOR-1
Immunogen: Synthetic peptide corresponding to aa 22-38 of rat MOP (μ-opioid receptor).
Source/Host: From rabbit.
Specificity: Recognizes rat MOP.
Application: Western Blot
Shipping: SHIPPED ON BLUE ICE
Long Term Storage: -20°C
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