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)

and a pseudogene of TCF3 is located on the short arm of chromosome 9

X-linked 3) encodes a member of the ALEX family of proteins which may play a role in tumor suppression

The encoded enzyme may function in two ways: to catalyze the biosynthesis of platelet-activating factor (1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine) from 1-O-alkyl-sn-glycero-3-phosphocholine

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),