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MOP (GP-non-phospho), µ-Opioid Receptor Antibody, Guinea Pig

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KO-Validated
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  • 7TM0319N-GP
  • 100 µl
  • Rabbit
The non-phospho-µ-opioid receptor antibody is directed against the distal end of the... more

The non-phospho-µ-opioid receptor antibody is directed against the distal end of the carboxyl-terminal tail of mouse, rat and human MOP. It detects selectively the canonical form of MOP and none of the putative splice variants. It can be used to detect total MOP receptors in Western blots independent of phosphorylation. The non-phospho-MOP antibody can also be used to isolate and enrich µ-opioid receptors from brain lysates. It also detects MOP in cultured cells and tissue sections by immunohistochemistry. 

  Alternative Names MOP, OPRM1, µ-Opioid Receptor, Mu Receptor IUPHAR... more

 

Alternative Names MOP, OPRM1, µ-Opioid Receptor, Mu Receptor
IUPHAR Target ID  319
UniProt ID  P35372 (human) P42866 (mouse) P33535 (rat)
Western Blot (WB)  1:1000
Immunohistochemistry (IHC) 1:100
Species Reactivity   Human, Mouse, Rat
Host / Isotype Guinea Pig / IgG
Class Polyclonal
Immunogen A synthetic peptide with the sequence  LENLEAETAPLP which is present in carboxyl-terminal tail of human, mouse and rat MOP
Form  Liquid
Purification Antigen affinity chromatography
Storage buffer Dulbecco's PBS, pH 7.4, with 150 mM NaCl, 0.02% sodium azide
Storage conditions short-term 4°C, long-term -20°C
Figure 1. Validation of the µ-Opioid Receptor in transfected HEK293 cells. Native HEK293... more

Figure 1. Validation of the µ-Opioid Receptor in transfected HEK293 cells. Native HEK293 cells (MOCK) or HEK293 cells stably expressing the µ-Opioid Receptor (MOP) were lysed and immunoblotted with the phosphorylation-independent anti-MOP antibody (7TM0319N-GP) at a dilution of 1:1000.

Figure 2. Immunohistochemical identification of µ-Opioid Receptor in Striatum. Sections were dewaxed, microwaved in citric acid, and incubated with anti-MOP (µ-Opioid Receptor) antibody (7TM0319N-GP) at a dilution of 1:100. Sections were then sequentially treated with biotinylated anti-rabbit IgG and avidin-biotin solution.Color was developed by incubation in 3-amino-9-ethylcarbazole (AEC), and sections were counterstained with hematoxylin. 


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