Search results for glutamate receptor

Glutamate Receptor 1 (GRIA1) Antibody, Abbexa, abx340126

GRIA1 Antibody is a Rabbit Polyclonal against GRIA1.

Glutamate Receptor 1 (GRIA1) Antibody, Abbexa, abx320074

GRIA1 Antibody is a Rabbit Polyclonal against GRIA1.

Metabotropic Glutamate Receptor 6 antibody, Covalab, Ref 00099374

Glutamate Receptor 1 (GRIA1) Antibody, Abbexa, abx001509

GRIA1 Antibody is a Rabbit Polyclonal antibody against GRIA1. Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes with multiple subunits, each possessing transmembrane regions, and all arranged to form a ligand-gated ion channel. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. This gene belongs to a family of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Metabotropic Glutamate Receptor 1a antibody, Covalab, Ref 00036336

metabotropic Glutamate Receptor 1a antibody, Covalab, Ref 00036388

Glutamate Receptor 1 (GRIA1) Antibody, Abbexa, abx010844

Glutamate Receptor 1 (GRIA1) Antibody is a Rabbit Polyclonal antibody for the detection of GRIA1.

mGluR1 / 5 glutamate receptor Antibody, Abbexa, abx445030

mGluR1/5 glutamate receptor Antibody is a Mouse Monoclonal antibody against mGluR1/5 glutamate receptor.

Glutamate Receptor 5 (GLUR5) Antibody, Abbexa, abx430343

GLuR5 Antibody is a Goat Polyclonal antibody against GLuR5.

Glutamate Receptor 2 (GRIA2) Antibody, Abbexa, abx000558

GRIA2 Antibody is a Rabbit Polyclonal antibody against GRIA2. Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to a family of glutamate receptors that are sensitive to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and function as ligand-activated cation channels. These channels are assembled from 4 related subunits, GRIA1-4. The subunit encoded by this gene (GRIA2) is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to render the channel impermeable to Ca(2+). Human and animal studies suggest that pre-mRNA editing is essential for brain function, and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology. Alternative splicing, resulting in transcript variants encoding different isoforms, (including the flip and flop isoforms that vary in their signal transduction properties), has been noted for this gene.