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NMDAR2B elisa kit

Phospho-NMDAR2B (Tyr1474) Colorimetric Cell-Based ELISA Kit

Gene Names
GRIN2B; NR3; MRD6; NR2B; hNR3; EIEE27; GluN2B; NMDAR2B
Reactivity
Human, Mouse, Rat
Synonyms
NMDAR2B; Phospho-NMDAR2B (Tyr1474) Colorimetric Cell-Based ELISA Kit; Glutamate [NMDA] receptor subunit epsilon 2 precursor; GRIN2B; hNR3; N-methyl D-aspartate receptor subtype 2B; N-methyl-D-aspartate receptor subtype 2B; N-methyl-D-aspartate receptor subunit 3; NMDE2; NME2; NR2B; NR3; NMDAR2B elisa kit
Ordering
For Research Use Only!
Reactivity
Human, Mouse, Rat
Form/Format
Two 96-Well Plates
Sequence Length
1484
Samples
Researchers plate their cell line of choice
Assay Type
Phospho Cell-Based ELISA
Sensitivity
>=5000 cells/well
Reactivity Note
Human: Y1474, Mouse: Y1472, Rat: Y1472
Detection Method
Colorimetric 450 nm
Preparation and Storage
Store at 4 degree C.
Product Categories/Family for NMDAR2B elisa kit

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
166367
NCBI Official Full Name
glutamate receptor ionotropic, NMDA 2B
NCBI Official Synonym Full Names
glutamate ionotropic receptor NMDA type subunit 2B
NCBI Official Symbol
GRIN2B
NCBI Official Synonym Symbols
NR3; MRD6; NR2B; hNR3; EIEE27; GluN2B; NMDAR2B
NCBI Protein Information
glutamate receptor ionotropic, NMDA 2B
UniProt Protein Name
Glutamate receptor ionotropic, NMDA 2B
UniProt Gene Name
GRIN2B
UniProt Synonym Gene Names
NMDAR2B; NR2B; NR3; hNR3

NCBI Description

This gene encodes a member of the N-methyl-D-aspartate (NMDA) receptor family within the ionotropic glutamate receptor superfamily. The encoded protein is a subunit of the NMDA receptor ion channel which acts as an agonist binding site for glutamate. The NMDA receptors mediate a slow calcium-permeable component of excitatory synaptic transmission in the central nervous system. The NMDA receptors are heterotetramers of seven genetically encoded, differentially expressed subunits including NR1 (GRIN1), NR2 (GRIN2A, GRIN2B, GRIN2C, or GRIN2D) and NR3 (GRIN3A or GRIN3B). The early expression of this gene in development suggests a role in brain development, circuit formation, synaptic plasticity, and cellular migration and differentiation. Naturally occurring mutations within this gene are associated with neurodevelopmental disorders including autism spectrum disorder, attention deficit hyperactivity disorder, epilepsy, and schizophrenia. [provided by RefSeq, Aug 2017]

Uniprot Description

NMDAR2B: an NMDA receptor subtype of glutamate-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Mediated by glycine. Plays a key role in synaptic plasticity, synaptogenesis, excitotoxicity, memory acquisition and learning. Mediates neuronal functions in glutamate neurotransmission. In concert with DAPK1 at extrasynaptic sites, acts as a central mediator for stroke damage. Its phosphorylation at Ser-1303 by DAPK1 enhances synaptic NMDA receptor channel activity inducing injurious Ca2+ influx through them, resulting in an irreversible neuronal death.

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

Chromosomal Location of Human Ortholog: 12p13.1

Cellular Component: cell junction; cell surface; integral component of plasma membrane; intracellular; neuron projection; NMDA selective glutamate receptor complex; plasma membrane; postsynaptic density; postsynaptic membrane

Molecular Function: extracellular-glutamate-gated ion channel activity; glutamate binding; glutamate-gated calcium ion channel activity; glycine binding; NMDA glutamate receptor activity; protein binding; Ras guanyl-nucleotide exchange factor activity; zinc ion binding

Biological Process: calcium-mediated signaling; ephrin receptor signaling pathway; excitatory postsynaptic potential; glutamate receptor signaling pathway; ionotropic glutamate receptor signaling pathway; learning and/or memory; MAPK cascade; positive regulation of neuron death; protein heterotetramerization; regulation of molecular function; response to ethanol; synaptic transmission; transport

Disease: Epileptic Encephalopathy, Early Infantile, 27; Mental Retardation, Autosomal Dominant 6

Research Articles on NMDAR2B

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Product Notes

The Human, Mouse, Rat NMDAR2B grin2b (Catalog #AAA9501130) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9501130 ELISA Kit recognizes Human, Mouse, Rat NMDAR2B. It is sometimes possible for the material contained within the vial of "NMDAR2B, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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