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GRIN2A, Polyclonal Antibody

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产品名称: GRIN2A, Polyclonal Antibody
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简单介绍

GRIN2A, Polyclonal Antibody


GRIN2A, Polyclonal Antibody  的详细介绍
Product Name

GRIN2A, Polyclonal Antibody

Full Product Name

GRIN2A antibody (N-terminus)

Product Synonym Names
Polyclonal GRIN2A; Anti-GRIN2A; GRIN 2A; GRIN-2A; GRIN2A; Glutamate Receptor Ionotropic N-Methyl D-Aspartate 2A; NMDAR2A; NR2A
Product Gene Name

anti-GRIN2A antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
138253
3D Structure
ModBase 3D Structure for Q12879
Clonality
Polyclonal
Host
Rabbit
Purity/Purification
GRIN2A antibody was purified by affinity chromatography
Form/Format
Supplied in liquid form in 10 mM HEPES buffer (pH 7.5), 150 mM NaCl, 100 ug per ml BSA and 50% glycerol
Biological Significance
NMDA receptor subtype of glutamate-gated ion channels possesses high calcium permeability and voltage-dependent sensitivity to magnesium. Activation requires binding of agonist to both types of subunits.
Other Notes
Small volumes of anti-GRIN2A antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-GRIN2A antibody
Rabbit polyclonal GRIN2A antibody (N-terminus)
Product Categories/Family for anti-GRIN2A antibody
Signal Transduction; Purified Polyclonal Antibodies
Applications Tested/Suitable for anti-GRIN2A antibody
Western Blot (WB), Immunohistochemistry (IHC)
Application Notes for anti-GRIN2A antibody
WB: 1:1000
IHC: 1:500

Immunofluorescence (IF) of anti-GRIN2A antibody
Immunofluorescent staining of 21 DIV nucleofected mouse striatal neuron (green) co-cultured with cortical neurons showing nice punctate labeling of the N-terminal NR2A subunit (red) in both the medium spiny neurons and the large pyramidal cell in the upper right
anti-GRIN2A antibody Immunofluorescence (IF) image
Western Blot (WB) of anti-GRIN2A antibody
Western blot of 10 ug of rat hippocampal lysate showing specific immunolabeling of ~ 180k NR2A subunit.
anti-GRIN2A antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for GRIN2A. It may not necessarily be applicable to this product.
NCBI GI #
197313638
NCBI GeneID
2903
NCBI Accession #
NP_001127880.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001134408.1 [Other Products]
UniProt Primary Accession #
Q12879 [Other Products]
UniProt Secondary Accession #
O00669; Q17RZ6[Other Products]
UniProt Related Accession #
Q12879[Other Products]
Molecular Weight
144,431 Da
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NCBI Official Full Name
glutamate receptor ionotropic, NMDA 2A isoform 2
NCBI Official Synonym Full Names
glutamate receptor, ionotropic, N-methyl D-aspartate 2A
NCBI Official Symbol
GRIN2A  [Similar Products]
NCBI Official Synonym Symbols
LKS; EPND; FESD; NR2A; GluN2A; NMDAR2A
  [Similar Products]
NCBI Protein Information
glutamate receptor ionotropic, NMDA 2A
UniProt Protein Name
Glutamate receptor ionotropic, NMDA 2A
UniProt Synonym Protein Names
Glutamate [NMDA] receptor subunit epsilon-1; N-methyl D-aspartate receptor subtype 2A; NMDAR2A; NR2A; hNR2A
Protein Family
Glutamate receptor ionotropic
UniProt Gene Name
GRIN2A  [Similar Products]
UniProt Synonym Gene Names
NMDAR2A; GluN2A; NMDAR2A; NR2A; hNR2A  [Similar Products]
UniProt Entry Name
NMDE1_HUMAN
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NCBI Summary for GRIN2A
This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
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UniProt Comments for GRIN2A
NMDAR2A: a subunit of N-methyl-D-aspartate (NMDA) receptors, members of the glutamate receptor channel superfamily. Possesses high calcium permeability and voltage-dependent sensitivity to magnesium and is modulated by glycine. Plays a key role in synaptic plasticity, synaptogenesis, excitotoxicity, memory acquisition and learning. Mediates neuronal functions in glutamate neurotransmission.

Protein type: Membrane protein, multi-pass; Membrane protein, integral; Channel, ligand-gated

Chromosomal Location of Human Ortholog: 16p13.2

Cellular Component: presynaptic membrane; postsynaptic membrane; synaptic vesicle; cell surface; integral to plasma membrane; endoplasmic reticulum; dendrite; plasma membrane; cell junction; N-methyl-D-aspartate selective glutamate receptor complex

Molecular Function: protein binding; extracellular-glutamate-gated ion channel activity; zinc ion binding; calcium channel activity; N-methyl-D-aspartate selective glutamate receptor activity

Biological Process: startle response; positive regulation of apoptosis; regulation of synaptic plasticity; sensory perception of pain; dopamine metabolic process; synaptic transmission; protein localization; learning and/or memory; transport; response to wounding; visual learning; serotonin metabolic process; response to drug; synaptic transmission, glutamatergic; glutamate signaling pathway; response to amphetamine; sleep; memory; response to ethanol; neurogenesis; directional locomotion; ionotropic glutamate receptor signaling pathway; regulation of sensory perception of pain; regulation of excitatory postsynaptic membrane potential; negative regulation of protein catabolic process

Disease: Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation
Research Articles on GRIN2A
1. Dysarthria and dyspraxia are found in individuals with GRIN2A mutations, often in the setting of epilepsy-aphasia syndromes. The speech phenotype may occur in the absence of a seizure disorder, reinforcing the role for GRIN2A in motor speech function.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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