NMDAEpsilon4 Polyclonal Antibody, 20ul[BT-AP06077] Shakers Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

Growth associated protein 43 is considered a crucial component of an effective regenerative response in the nervous system

A related pseudogene has been identified on chromosome 19

This protein localizes to the endoplasmic reticulum and is thought to be the predominant enzyme responsible for epoxidation of endogenous arachidonic acid in cardiac tissue

GPR149 (G Protein-Coupled Receptor 149) is a Protein Coding gene

NMDAEpsilon4 Polyclonal Antibody, 20ul[BT-AP06077] Shakers Mutations in this gene haveN methyl D aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. NMDA channel has been shown to be involved in long term potentiation, an activity dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDA receptor channels are heteromers composed of the key receptor subunit NMDAR1 (GRIN1) and 1 or more of the 4 NMDAR2 subunits: nMDAR2A (GRIN2A), NMDAR2B (GRIN2B),