Glutamate Metabotropic Receptor 6 (GRM6) Antibody

Este producto es parte de GRM - Glutamate Receptor Metabotropic
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221€ (50 µg)

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935106861
info@markelab.com
name
Glutamate Metabotropic Receptor 6 (GRM6) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx324501
tested applications
ELISA, WB, IHC

Description

GRM6 Antibody is a Rabbit Polyclonal against GRM6.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Glutamate Metabotropic Receptor 6 (GRM6)
Host
Rabbit
Reactivity
Human
Recommended Dilution
ELISA: 1/20000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/300. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
50 µg
Size 2
100 µg
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O15303
Gene ID
2916
Alias
GRM6,CSNB1B,GPRC1F,MGLUR6,mGlu6,nob4,nerg1,nob2,nob3
Background
Antibody anti-GRM6
Status
RUO

Descripción

GRM6, or mGluR6, is a Group III metabotropic glutamate receptor primarily expressed in the retina, where it plays a critical role in visual signal transmission. GRM6 is located on the dendrites of ON bipolar cells, where it couples to Gi/o proteins to inhibit adenylate cyclase, reducing cAMP levels. This pathway is essential for detecting light changes and relaying visual signals from photoreceptors to the brain. Mutations in the GRM6 gene are associated with congenital stationary night blindness (CSNB), a condition characterized by impaired night vision and abnormal signal transduction in the retina. Beyond its role in vision, GRM6 may have limited expression in the CNS, where it could contribute to inhibitory neurotransmission. Given its specialized function in the retina, GRM6 represents a key target for understanding retinal disorders and developing therapies to restore visual signaling in hereditary visual impairments.

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