Mu-type opioid receptor Phospho-Ser375 (OPRM1 pS375) Antibody

Este producto es parte de OPR - Opioid Receptor
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429€ (100 µl)

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935106861
info@markelab.com
name
Mu-type opioid receptor Phospho-Ser375 (OPRM1 pS375) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx333375
tested applications
ELISA, WB

Description

OPRM1 (pS375) Antibody is a Rabbit Polyclonal against OPRM1 (pS375).

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Mu-type opioid receptor Phospho-Ser375 (OPRM1 pS375)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Assay Data
Modification: Phosphorylation // Target Modification: Ser375
Recommended Dilution
WB: 1/500 - 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS (without Mg2+ and Ca2+), pH 7.4, containing 150mM NaCl, 0.02% sodium azide and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P35372
Gene ID
4988
Alias
OPRM1,Mu receptor,MOP,OP3,MOPr,opioid receptor,mu 1,opioid receptor,MOR,LMOR,MOR1,OPRM,M-OR-1
Background
Antibody anti-OPRM1
Status
RUO

Descripción

OPRM1, or the mu-opioid receptor, is the primary target for endogenous opioid peptides like endorphins and exogenous opioids such as morphine, fentanyl, and heroin. OPRM1 is highly expressed in pain-processing regions of the CNS, including the brainstem, thalamus, and spinal cord, where it mediates analgesia, euphoria, and sedation. OPRM1 couples to Gi/o proteins, inhibiting adenylate cyclase, reducing cAMP levels, and modulating ion channels to decrease neuronal excitability and neurotransmitter release. Activation of OPRM1 produces potent analgesic effects but also carries risks of tolerance, dependence, and respiratory depression. Dysregulation of OPRM1 signaling is central to opioid addiction, chronic pain, and reward pathways. Selective modulation of OPRM1 has therapeutic potential for improving pain management while reducing side effects such as tolerance and dependence. Biased agonists that preferentially activate analgesic pathways over adverse effects are under development to enhance safety. OPRM1 remains a key target for opioids and therapies addressing addiction and pain disorders.

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