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pT370-MOP (phospho-µ-Opioid Receptor Antibody)

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  • 7TM0319B
  • 100 µl
  • Rabbit
Threonine370 (T370) is a major phosphorylation site of the µ-opioid receptor (MOP). The... more

Threonine370 (T370) is a major phosphorylation site of the µ-opioid receptor (MOP). The pT370-MOP antibody detects phosphorylation in response to high-efficacy agonists but to low-efficacy agonists. The pT370-MOP antibody also detects phosphorylation  after PKC activation. T370 phosphorylation is a key regulator of MOP desensitization, β-arrestin recruitment and tolerance.

  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
Species Reactivity   Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Immunogen A synthetic phosphopeptide derived from human MOP around the phosphorylation site of Thr370
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. Agonist-induced Threonine370 phosphorylation of the µ-opioid receptor. Upper panel,... more

Figure 1. Agonist-induced Threonine370 phosphorylation of the µ-opioid receptor. Upper panel, HEK293 cells stably expressing the µ-opioid receptor (MOP) were either not exposed or exposed to 10 μM DAMGO ([D-Ala2,N-MePhe4, Gly-ol]-enkephalin) or 0.1 μM PMA (Phorbol 12-Myristate 13-Acetate) for 30 minutes. Cells were lysed and immunoblotted with the anti-pT370-MOP antibody (7TM0319B) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-MOP antibody (7TM0319N-WB) at a dilution of 1:1000 to confirm equal loading of the gel.

Figure 2. Analysis of dose-dependent µ-opioid receptor phosphorylation using a panel of phosphosite-specific antibodies. Upper four panels, HEK293 cells stably expressing the µ-opioid receptor (MOP) were either not exposed or exposed to increasing concentrations of DAMGO ([D-Ala2,N-MePhe4, Gly-ol]-enkephalin) ranging from 1 nM to 1 μM for 30 minutes. Cells were lysed and immunoblotted with the anti-pT370-MOP antibody (7TM0319B) or anti-pS375-MOP antibody (7TM0319C) or anti-pT376-MOP antibody (7TM0319D) or anti-pT379-MOP antibody (7TM0319E) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-MOP antibody (7TM0319N-WB) at a dilution of 1:1000 to confirm equal loading of the gel. Note, Serine375 is the primary site of phosphorylation.

Figure 3. Analysis of agonist-selective µ-opioid receptor phosphorylation using a panel of phosphosite-specific antibodies. Upper 4 panels, HEK293 cells stably expressing the µ-opioid receptor (MOP) were either not exposed or exposed to 10 µM morphine or 10 µM DAMGO ([D-Ala2,N-MePhe4, Gly-ol]-enkephalin) for 30 minutes. Cells were lysed and immunoblotted with the anti-pT370-MOP antibody (7TM0319B) or anti-pS375-MOP antibody (7TM0319C) or anti-pT376-MOP antibody (7TM0319D) or anti-pT379-MOP antibody (7TM0319E) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-MOP antibody (7TM0319N-WB) at a dilution of 1:1000 to confirm equal loading of the gel. Note, DAMGO induces multisite phosphorylation. Morphine induces primarily the phosphorylation of Serine375.

Figure 4. Blocking of PMA-mediated Threonine370 phosphorylation of the µ-opioid receptor. Upper panel, HEK293 cells stably expressing the µ-opioid receptor (MOP) were either not exposed or exposed to 0.1 μM PMA (Phorbol 12-Myristate 13-Acetate) in presence or absence of kinase inhibitor Staurosporine (10 µM) for 30 minutes. Cells were lysed and immunoblotted with the anti-pT370-MOP antibody (7TM0319B) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-MOP antibody (7TM0319N-WB) at a dilution of 1:1000 to confirm equal loading of the gel.

Kliewer A, Schmiedel F, Sianati S, Bailey A, Bateman JT, Levitt ES, Williams JT, Christie MJ,... more

Kliewer A, Schmiedel F, Sianati S, Bailey A, Bateman JT, Levitt ES, Williams JT, Christie MJ, Schulz S. Phosphorylation-deficient G-protein-biased μ-opioid receptors improve analgesia and diminish tolerance but worsen opioid side effects. Nat Commun. 2019 Jan 21;10(1):367. doi: 10.1038/s41467-018-08162-1. PubMed PMID: 30664663; PubMed Central PMCID: PMC6341117.

Miess E, Gondin AB, Yousuf A, Steinborn R, Mösslein N, Yang Y, Göldner M, Ruland JG, Bünemann M, Krasel C, Christie MJ, Halls ML, Schulz S, Canals M. Multisite phosphorylation is required for sustained interaction with GRKs and arrestins during rapid μ-opioid receptor desensitization. Sci Signal. 2018 Jul 17;11(539). pii: eaas9609. doi: 10.1126/scisignal.aas9609. PubMed PMID: 30018083.

Yousuf A, Miess E, Sianati S, Du YP, Schulz S, Christie MJ. Role of Phosphorylation Sites in Desensitization of µ-Opioid Receptor. Mol Pharmacol. 2015 Oct;88(4):825-35. doi: 10.1124/mol.115.098244. Epub 2015 May 12. PubMed PMID: 25969388.

Just S, Illing S, Trester-Zedlitz M, Lau EK, Kotowski SJ, Miess E, Mann A, Doll C, Trinidad JC, Burlingame AL, von Zastrow M, Schulz S. Differentiation of opioid drug effects by hierarchical multi-site phosphorylation. Mol Pharmacol. 2013 Mar;83(3):633-9. doi: 10.1124/mol.112.082875. Epub 2012 Dec 13. PubMed PMID: 23239825; PubMed Central PMCID: PMC3583494.

Doll C, Pöll F, Peuker K, Loktev A, Glück L, Schulz S. Deciphering µ-opioid receptor phosphorylation and dephosphorylation in HEK293 cells. Br J Pharmacol. 2012 Nov;167(6):1259-70. doi: 10.1111/j.1476-5381.2012.02080.x. PubMed PMID: 22725608; PubMed Central PMCID: PMC3504992.

Doll C, Konietzko J, Pöll F, Koch T, Höllt V, Schulz S. Agonist-selective patterns of µ-opioid receptor phosphorylation revealed by phosphosite-specific antibodies. Br J Pharmacol. 2011 Sep;164(2):298-307. doi: 10.1111/j.1476-5381.2011.01382.x. PubMed PMID: 21449911; PubMed Central PMCID: PMC3174411.

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