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GRIN2B Antibody

CAT: 0864-A74662-100ULSize: 100 µLDry Ice: NoHazardous: No
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CAT#:0864-A74662-100ULSize:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
AW490526, EIEE27, Glutamate [NMDA] receptor subunit epsilon 2, Glutamate [NMDA] receptor subunit epsilon-2, Glutamate Receptor Ionotropic N Methyl D Aspartate 2B, Glutamate Receptor Ionotropic N Methyl D Aspartate subunit 2B, Glutamate receptor ionotropic NMDA2B, Glutamate receptor subunit epsilon 2, Glutamate receptor, ionotropic, NMDA2B (epsilon 2) , GRIN 2B, GRIN2B, hNR 3, hNR3, MGC142178, MGC142180, MRD6, N methyl D asparate receptor channel subunit epsilon 2, N methyl D aspartate receptor subtype 2B, N methyl D aspartate receptor subunit 2B, N methyl D aspartate receptor subunit 3, N-methyl D-aspartate receptor subtype 2B, N-methyl-D-aspartate receptor subunit 3, NMDA NR2B, NMDA R2B, NMDAR2B, NMDE2, NMDE2_HUMAN, NME2, NR2B, NR3
UniProt
Q13224
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse, Rat
Target Antigen
Synthetic peptide of Human GRIN2B
Target
GRIN2B
Clonality
Polyclonal
Conjugation
Non-conjugated
Field of Research
Neuroscience
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.05% sodium azide, 40% glycerol, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · Q13224

Glutamate receptor ionotropic, NMDA 2B

NMDE2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q13224
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GRIN2B
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
GluN2B
EC number
—
Processing
Precursor
Secondary accessions
Q12919, Q13220, Q13225, Q14CU4, Q9UM56
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Ligand

CalciumMagnesiumMetal-bindingZinc

Cellular component

Cell membraneCell projectionCytoplasmCytoskeletonEndosomeLysosomeMembranePostsynaptic cell membraneSynapse

Coding sequence diversity

Chromosomal rearrangement

Disease

Disease variantEpilepsyIntellectual disability

PTM

Disulfide bondGlycoproteinPhosphoprotein

Molecular function

Ion channelLigand-gated ion channelReceptor

Biological process

Ion transportTransport

Domain

SignalTransmembraneTransmembrane helix

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