NMDAR2A/GRIN2A Rekombinanter Antikörper

NMDAR2A/GRIN2A Rekombinant Antikörper für WB, IF-P, FC (Intra), Cytometric bead array, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

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

Konjugation

Unkonjugiert

CloneNo.

240445D4

Kat-Nr. : 83465-2-PBS

Synonyme

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



Geprüfte Anwendungen

Produktinformation

83465-2-PBS bindet in WB, IF-P, FC (Intra), Cytometric bead array, Indirect ELISA NMDAR2A/GRIN2A und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
Wirt / Isotyp Kaninchen / IgG
Klonalität Rekombinant
Typ Antikörper
Immunogen NMDAR2A/GRIN2A fusion protein Ag29101
Vollständiger Name glutamate receptor, ionotropic, N-methyl D-aspartate 2A
Berechnetes Molekulargewicht 165 kDa
Beobachtetes Molekulargewicht160-180 kDa
GenBank-ZugangsnummerNM_000833
Gene symbol GRIN2A
Gene ID (NCBI) 2903
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

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.