Anti-NMDAR2B antibody - C-terminal,Abcam,AB229636

Host

Rabbit

Reactivity

Mouse, Rat

Application

IHC-P, WB, ICC/IF

Platform ID

BAB590494571

Abcam

Headquarters

Discovery Drive Cambridge Biomedical Campus Cambridge CB2 0AX UK

Contact

Tel: +44 (0)1223 696000
Fax: +44 (0)1223 215 215

Product Specifications
Scientific Background

Specifications

NameAnti-NMDAR2B antibody - C-terminal
Cat. No.AB229636
HostRabbit
IsotypeIgG
ReactivityMouse, Rat
ApplicationIHC-P, WB, ICC/IF
ClonalityPolyclonal
Concentration0.44 mg/mL Batch dependent concentration
ImmunogenSynthetic Peptide within Rat Grin2b aa 1400 to C-terminus. The exact immunogen used to generate this antibody is proprietary information.
PurityAffinity purification Immunogen
Appearance/FormLiquid
ShippingBlue Ice
FormulationpH: 7 Preservative: 0.025% Proclin 300 Constituents: PBS, 20% Glycerol (glycerin, glycerine), 1% BSA
Storage-20°C
Regulatory StatusResearch Use Only

Scientific Background

Target data Component of N-methyl-D-aspartate (NMDA) receptors (NMDARs) that function as heterotetrameric, ligand-gated cation channels with high calcium permeability and voltage-dependent block by Mg(2+) (PubMed : 11929923, PubMed : 19910922, PubMed : 21677647, PubMed : 24607230, PubMed : 24876489, PubMed : 27135925, PubMed : 7524561). Participates in synaptic plasticity for learning and memory formation by contributing to the long-term depression (LTD) of hippocampus membrane currents (By similarity). Channel activation requires binding of the neurotransmitter L-glutamate to the GluN2 subunit, glycine or D-serine binding to the GluN1 subunit, plus membrane depolarization to eliminate channel inhibition by Mg(2+) (PubMed : 11929923, PubMed : 19910922, PubMed : 21677647, PubMed : 24607230, PubMed : 24876489, PubMed : 27135925, PubMed : 7524561). NMDARs mediate simultaneously the potasium efflux and the influx of calcium and sodium (By similarity). Each GluN2 subunit confers differential attributes to channel properties, including activation, deactivation and desensitization kinetics, pH sensitivity, Ca2(+) permeability, and binding to allosteric modulators (PubMed : 10436042, PubMed : 11929923, PubMed : 24607230, PubMed : 9463421). In concert with DAPK1 at extrasynaptic sites, acts as a central mediator for stroke damage (By similarity). 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 (By similarity). See full target information Grin2b

Category Paths

Request a product

Please provide the required information below so that we can quickly source your products.