Metabotropic Glutamate Receptor 5 (GRM5) Antibody (PE)

Este producto es parte de GRM - Glutamate Receptor Metabotropic
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637€ (100 µg)

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935106861
info@markelab.com
name
Metabotropic Glutamate Receptor 5 (GRM5) Antibody (PE)
category
Primary Antibodies
provider
Abbexa
reference
abx444392
tested applications
WB, IHC, IF/ICC, IP

Description

mGluR1/5 Glutamate Receptor Antibody is a Mouse Monoclonal conjugated to PE against mGluR5.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Metabotropic Glutamate Receptor 5 (GRM5)
Host
Mouse
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/1000, IHC: 1/1000, IF/ICC: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
PE
Isotype
IgG2A
Purification
Purified by Protein G.
Size 1
100 µg
Tested Applications
WB, IHC, IF/ICC, IP
Buffer
PBS, pH 7.4, 50% glycerol, 0.09% sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P31424
Gene ID
24418
NCBI Accession
NP_058708.1
Alias
GRM5,GPRC1E,MGLUR5,PPP1R86,mGlu5
Background
Antibody anti-GRM5
Status
RUO
Note
Concentration: 1 mg/ml - 

Descripción

GRM5, or mGluR5, is a Group I metabotropic glutamate receptor that couples to Gq proteins, activating phospholipase C (PLC), increasing intracellular calcium levels, and triggering downstream signaling pathways such as MAPK and PI3K/Akt. GRM5 is primarily expressed in the hippocampus, cortex, and basal ganglia, where it regulates synaptic plasticity, learning, and memory formation. It also modulates long-term potentiation (LTP) and excitotoxic responses. Dysregulation of GRM5 is implicated in neurological and psychiatric disorders, including fragile X syndrome, autism spectrum disorders (ASD), schizophrenia, and addiction. GRM5 overactivation can exacerbate excitotoxicity, leading to neurodegeneration in diseases like Alzheimer’s and Parkinson’s. Antagonists of GRM5, such as selective negative allosteric modulators (NAMs), are being explored for treating neurodevelopmental disorders, anxiety, and addiction. Targeting GRM5 holds significant promise for improving synaptic function and reducing excitotoxic damage in CNS-related diseases.

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L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 (also known as GPRC1E) and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. The activity of GRM5 is mediated by a G-protein that activates a phosphatidylinositol-calcium second messenger system and generates a calcium-activated chloride current.

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