Ionotropic Glutamate receptor 2 Rabbit Monoclonal Antibody

Ionotropic Glutamate receptor 2 Rabbit Monoclonal Antibody

Cat: AMRe87466
Size:50μL Price:$168
Size:100μL Price:$300
Application:WB,IHC,IP

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:Ionotropic Glutamate receptor 2
Category: Recombinant Monoclonal Antibody Tags: , , , , , , ,

Summary

Production Name

Ionotropic Glutamate receptor 2 Rabbit Monoclonal Antibody

Description

Recombinant rabbit monoclonal antibody

Host

Rabbit

Application

WB,IHC,IP

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

Ionotropic Glutamate receptor 2

Alternative Names

GLUR2; GLURB; GluA2; HBGR2; GluR-K2

Gene ID

2891

SwissProt ID

P42262

 

Application

Dilution Ratio

WB 1:500-1:2000,IHC 1:200-1:500,IP 1:20-1:50

Molecular Weight

Calculated MW:99 kDa; Observed MW:99 kDa

 

Background

Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to a family of glutamate receptors that are sensitive to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and function as ligand-activated cation channels. These channels are assembled from 4 related subunits, GRIA1-4. The subunit encoded by this gene (GRIA2) is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to render the channel impermeable to Ca(2+). Human and animal studies suggest that pre-mRNA editing is essential for brain function, and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology. Alternative splicing, resulting in transcript variants encoding different isoforms, (including the flip and flop isoforms that vary in their signal transduction properties), has been noted for this gene. [provided by RefSeq, Jul 2008]

 

Research Area

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