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SMC-419D-APC

mGluR1/5 Antibody, Clone N75/3: APC

Cannot supply to this region.

SKU:
SMC-419D-APC
Additional Names:
mGluR5, mGlu5, GRM5, GPRC1E, Metabotropic glutamate receptor 5, Metabotropic glutamate receptor 5 variant F, Metabotropic glutamate receptor 5 variant G, Metabotropic glutamate receptor 5 variant H, Glutamate receptor metabotropic 5, mGluR5a, mGluR5b, mGluR, Glutamate receptor metabotropic 1, mGlu1, mGluR1, GRM1, GRM 1, GRM1A, GRM1 alpha, GRM1_HUMAN, GPRC1A, Metabotropic glutamate receptor 1, mGluR1 alpha
Application:
IHC, WB, IF, ICC, IP
Concentration:
1 mg/ml
Species Reactivity:
Rat
Purification:
Protein G Purified
Storage Conditions:
See Manual
Supplier:
StressMarq Biosciences
Host:
Mouse
Reactivities:
Human, Mouse, Rat
Buffer:
95.46mM Phosphate, 2.48mM MES and 2mM EDTA
Immunogen:
Fusion protein amino acids 824-1203 (cytoplasmic C-terminus) of rat mGluR5b
Clone:
N75/3 (Formerly sold as S75-3)
Uniprot:
P31424
Synonyms:
glutamate receptor, metabotropic 5;metabotropic glutamate receptor (mGluR5);metabotropic glutamate receptor 5;metabotropic glutamate receptor 5b;mGluR5
Extra Details:
mGluR5 (metabotropic glutamate receptor 5) is a subtype of glutamate receptor that regulates synaptic transmission and plasticity via G-protein-coupled signaling. It is predominantly expressed in the hippocampus, cortex, and striatum-regions vulnerable to neurodegeneration. Aberrant mGluR5 activity has been linked to excitotoxicity, calcium dysregulation, and neuroinflammation, contributing to the pathophysiology of Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS). mGluR5 also interacts with amyloid precursor protein and tau, influencing their aggregation and toxicity. Pharmacological modulation of mGluR5 has shown promise in preclinical models, where antagonists reduce neuronal loss and improve cognitive outcomes. As a key regulator of glutamatergic tone, mGluR5 is a compelling target for therapeutic intervention in neurodegenerative disorders characterized by synaptic dysfunction and excitatory imbalance.
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