Anticorps Recombinant de lapin anti-NMDAR2A/GRIN2A

NMDAR2A/GRIN2A Recombinant Antibody for WB, IF-P, FC (Intra), Cytometric bead array, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, IF-P, FC (Intra), Cytometric bead array, Indirect ELISA

Conjugaison

Non conjugué

CloneNo.

240445D4

N° de cat : 83465-2-PBS

Synonymes

GRIN2A, NMDAR2A, 240445D4, glun2a, Glutamate [NMDA] receptor subunit epsilon-1



Informations sur le produit

83465-2-PBS cible NMDAR2A/GRIN2A dans les applications de WB, IF-P, FC (Intra), Cytometric bead array, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Hôte / Isotype Lapin / IgG
Clonalité Recombinant
Type Anticorps
Immunogène NMDAR2A/GRIN2A Protéine recombinante Ag29101
Nom complet glutamate receptor, ionotropic, N-methyl D-aspartate 2A
Masse moléculaire calculée 165 kDa
Poids moléculaire observé160-180 kDa
Numéro d’acquisition GenBankNM_000833
Symbole du gène GRIN2A
Identification du gène (NCBI) 2903
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

GRIN2A (glutamate ionotropic receptor NMDA type subunit 2A), also known as NMDAR2A. And its molecular weight is 165 kDa. GRIN2A is located in cell projection, dendritic spine, cell membrane, synapse, postsynaptic cell membrae, cytolamic vesicle membrane, which is expressed in many tissues, highest expression in brain and heart. This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants.

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