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NMDAR2B (Ab-1336) polyclonal antibody

CAT: 0013-GTR18048487-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR18048487-01Size:50 μL
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Description
Rabbit polyclonal antibody to NMDAR2B (Ab-1336)
Product Name Alternative
GRIN2A; NMDAR2A; Glutamate [NMDA] receptor subunit epsilon-1; N-methyl D-aspartate receptor subtype 2A; NMDAR2A; NR2A; hNR2A; GRIN2B; NMDAR2B; Glutamate [NMDA] receptor subunit epsilon-2; N-methyl D-aspartate receptor subtype 2B; NMDAR2B; N
UniProt
Q13224
Reactivity
Human
Immunogen
The antiserum was produced against synthesized peptide derived from human NMDAR2A/B around the phosphorylation site of Tyr1246/1252. AA range:1216-1265
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1mg/ml
Dilution
ICC: 1: 100-300, IF: 1: 200-1000, ELISA: 1: 10000
Form
Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.02% sodium azide.
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, IF, IHC-P, WB
Host or Source
Rabbit
Preservative
Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.02% sodium azide.

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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