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Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody

Mu-type opioid receptor, Opioid receptor B, MOR-1, MOP, Mu-opiate receptor

Cat #: AOR-011
Alternative Name Mu-type opioid receptor, Opioid receptor B, MOR-1, MOP, Mu-opiate receptor
Lyophilized Powder yes
Type: Polyclonal
Host: Rabbit
Reactivity: h, m, r
  • Peptide CSPAPGSWLNLSHVDGN, corresponding to amino acid residues 22-38 of the rat µ-Opioid receptor (Accession P33535). Extracellular, N-terminus.
Accession (Uniprot) Number P33535
Gene ID 25601
Peptide confirmation Confirmed by amino acid analysis and mass spectrometry.
Homology Mouse - identical; human - 15/17 amino acid residues identical.
RRID AB_2040044.
Purity Affinity purified on immobilized antigen.
Form Lyophilized powder. Reconstituted antibody contains phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.05% NaN3.
Isotype Rabbit IgG.
Storage before reconstitution The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.
Reconstitution 25 μl, 50 μl or 0.2 ml double distilled water (DDW), depending on the sample size.
Antibody concentration after reconstitution 0.8 mg/ml.
Storage after reconstitution The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).
Standard quality control of each lot Western blot analysis.
Applications: ic, if, ifc, ih, lci, wb
May also work in: ip*
Western blot
  • Expression of µ-opioid receptor (MOR-1) in rat spinal cord
    Expression of µ-opioid receptor (MOR-1) in rat spinal cord
    Immunohistochemical staining of rat spinal cord frozen section using Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011), (1:100), followed by goat anti-rabbit AlexaFluor-488 secondary antibody (green). Staining is present in both neuronal cell bodies (white arrows) and their prolongations (red arrows). Hoechst 33342 is used as the counterstain (blue).
  • Rat neonatal drenomedullary chromaffin cells (AMCs) (Salman, S. et al. (2013) J. Physiol. 591, 515.).
Indirect flow cytometry
  • Cell surface detection of µ-Opioid Receptor in live intact mouse BV-2 microglia cells:
    Cell surface detection of µ-Opioid Receptor in live intact mouse BV-2 microglia cells:
    ___ Cells.
    ___ Cells + goat-anti-rabbit-FITC.
    ___ Cells + Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011), (5 µg) + goat-anti-rabbit-FITC.
Live cell imaging / Immunocytochemistry
  • Expression of µ-opioid receptor (MOR-1) in rat C6 cells
    Expression of µ-opioid receptor (MOR-1) in rat C6 cells
    Cell surface detection of µ-opioid receptor (MOR-1) in intact living rat brain glioma (C6) cells. A. Extracellular staining of cells using Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011), (1:300), (red). B. Merged image of A with live view of cell.
  1. Pan, L. et al. (2005) Neuroscience 133, 209.
  2. Matthes, H.W. et al. (1998) J. Neurosci. 18, 7285.
  3. Shaqura, M.A. et al. (2004) J. Pharmacol. Exp. Ther. 308, 712.
  4. Baraldi, P.G. et al. (2006) Curr. Med. Chem. 13, 3467.
Scientific background

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 kappa (κ)-opioid (KOP) receptor. Recently, the nociceptin/orphanin FQ (N/OFQ) peptide (NOP) receptor was also described. Despite its significant sequence homology, its pharmacological profile differs greatly from those of the classic µ, δ, and κ receptors.1

The opioid receptors belong to the G protein-coupled receptor (GPCR) superfamily whose members share a common structure of seven putative transmembrane domains, an extracellular amino terminus, a cytoplasmic carboxyl terminus, and a third intracellular loop important for binding G proteins.2

All three receptors mediate opioid-induced analgesia. Supraspinal analgesia is mainly mediated by the µ-receptors, whereas µ-, δ-, and κ-receptors participate in the control of pain at the spinal level. These receptors also mediate the mood-altering properties of opioids.3

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 heroin.1 The µ-opioid receptors are expressed in the central nervous system (CNS) and in the peripherial nervous system.  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 analgesia.4

Application key:

CBE- Cell-based ELISA, FC- Flow cytometry, ICC- Immunocytochemistry, IE- Indirect ELISA, IF- Immunofluorescence, IFC- Indirect flow cytometry, IHC- Immunohistochemistry, IP- Immunoprecipitation, LCI- Live cell imaging, N- Neutralization, WB- Western blot

Species reactivity key:

H- Human, M- Mouse, R- Rat
Image & Title: Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody
Expression of µ-Opioid Receptor in rat brain.Immunohistochemical staining of rat brain sections using Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011). MOR-1 expression is shown at the level of the anterior cingulate cortex (ACC), (A, B). Local ablation of MOR-1 staining using Derm-SAP (a cytotoxic ribosome inhibitor) abolishes MOR-1 staining (C). D, E. show higher magnification of the rectangular area of B and C, respectively.Adapted from Navratilova, E. et al. (2015) J. Neurosci. 35, 7264. with permission of the Society for Neuroscience.
Last update: 08/01/2023

Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011) is a highly specific antibody directed against an epitope of the rat protein. The antibody can be used in western blot, immunohistochemistry, live cell imaging, and indirect live cell flow cytometry applications. It has been designed to recognize MOR-1 from rat, human, and mouse samples.

For research purposes only, not for human use



Published figures using this product
  • Expression of μ- and δ-opioid receptors in immortalized rat chromaffin (MAH) cells.
    Expression of μ- and δ-opioid receptors in immortalized rat chromaffin (MAH) cells.
    Immunocytochemical staining of immortalized rat chromaffin (MAH) cells. A, C. Phase contrast image of MAH cells. B, D. Staining of cells with Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (#AOR-011), (B) and Anti-δ-Opioid Receptor (OPRD1) (extracellular) Antibody (#AOR-014), (D). E, G. Phase contrast image of MAH cells. F, H. Anti-µ-Opioid Receptor (OPRM1) (extracellular) Antibody (F) and Anti-δ-Opioid (OPRD1) Receptor (extracellular) antibody were incubated prior to incubation with cells.
    Adapted from Salman, S. et al. (2014) with permission of the American Physiological Society.
Western blot citations
  1. Rat DRG lysate.
    Ferrari, L.F. et al. (2019) Neuroscience 398, 64.
Immunohistochemistry citations
  1. Rat brain sections.
    Navratilova, E. et al. (2015) J. Neurosci. 35, 7264.
Immunocytochemistry citations
  1. Rat immortalized chromaffin (MAH) cells.
    Salman, S. et al. (2014) Am. J. Physiol. 307, C266.
  2. Rat neonatal adrenomedullary chromaffin cells (AMCs).
    Salman, S. et al. (2013) J. Physiol. 591, 515.


Scientific Background

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