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Anti-GRIN1/NMDAR1 Recombinant Antibody (ART5803) (HC465053)

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Overview
Catalog No.HC465053
Description
Anti-GRIN1/NMDAR1 Antibody (ART5803) [ART5803] (HC465053) is a human monoclonal antibody detecting NMDAR1 in ELISA, FACS, Functional assay. Suitable for Human.
Highlights
  • Multi-Application — Validated across multiple applications.
Species reactivityHuman
ApplicationsELISA, FACS, Functional assay
Host speciesHuman
IsotypeIgG1(L234A, L235A), kappa
Clone IDART5803
Clonality Monoclonal
Target GRIN1, GluN1, Glutamate [NMDA] receptor subunit zeta-1, Glutamate receptor ionotropic, NMDA 1, N-methyl-D-aspartate receptor subunit NR1, NMD-R1, NMDAR1, hNR1
Endotoxin level Please contact with the lab for this information.
Purity >95% as determined by SDS-PAGE.
Purification Protein A/G purified from cell culture supernatant.
Accession Q05586
Form Liquid
Storage buffer 0.01M PBS pH 7.4

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
ELISA 1:2000-1:20000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

Glutamate receptor ionotropic, NMDA 1 (GRIN1/NMDAR1) is a ~105 kDa protein. 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+). NMDARs participate in synaptic plasticity for learning and memory formation by contributing to the long-term potentiation (LTP). 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+). NMDARs mediate simultaneously the potassium efflux and the influx of calcium and sodium. Each GluN2 or GluN3 subunit confers differential attributes to channel properties, including activation, deactivation and desensitization kinetics, pH sensitivity, Ca2(+) permeability, and binding to allosteric modulators.

1. Hamdan, FF. et al. (2011) American journal of human genetics 88, 306-16. PMID: 21376300
2. Hackos, DH. et al. (2016) Neuron 89, 983-99. PMID: 26875626
3. Volgraf, M. et al. (2016) Journal of medicinal chemistry 59, 2760-79. PMID: 26919761
4. Chen, W. et al. (2017) Molecular pharmacology 91, 317-330. PMID: 28126851
5. Chen, W. et al. (2017) Journal of human genetics 62, 589-597. PMID: 28228639
6. Zhang, J. et al. (2023) Nature structural & molecular biology 30, 629-639. PMID: 36959261
7. Karp, SJ. et al. (1993) The Journal of biological chemistry 268, 3728-33. PMID: 7679115
8. Younkin, DP. et al. (1993) Proceedings of the National Academy of Sciences of the United States of America 90, 2174-8. PMID: 7681588
9. Planells-Cases, R. et al. (1993) Proceedings of the National Academy of Sciences of the United States of America 90, 5057-61. PMID: 7685113
Note For research use only
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Formula
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