Methyl butetisalicylate

[(2R)-1-methylpyrrolidin-2-yl]methanamine.

[(3R)-1-methylpyrrolidin-3-yl]methanamine.

General description This gene encodes a protein that has some similarity to N2,N2-dimethylguanosine tRNA methyltransferase from other organisms. Studies of the mouse ortholog have shown that this protein plays a role in motor coordination and

Anti-CEP290 centrosomal protein 290kDa, 25ul UN 1687 6.1 PG2

General description DDAH (Dimethylarginine dimethylaminohydrolase) exists as two isoforms: DDAH1, and DDAH2. Tissues expressing endothelial nitric oxide synthases is predominated by DDAH2.

General description The encoded protein catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine. Defects in this gene are the cause of aromatic

Trisomy of human chromosome 21 result in patients with Down&#8242s syndrome, which is a complex developmental and neurodegenerative disease that is characterized with abnormal morphological features, hypotonia, and mental retardation. The DSCR3

Specificity Recognizes an epitope common to Glutamate Receptors 5, 6 and 7. No reactivity seen to GluR1, GluR2, GluR3 or GluR4.

Immunogen Synthetic peptide directed towards the middle region of human GRIN2A Biochem/physiol Actions N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate-gated ion channels. These receptors have been shown to be involved

LMX-1 is a transcription factor that belongs to the LIM-homeodomain (LIM-HD) transcription factor family. It is induced within the ventral midbrain as a response to early signaling.

General description Glutamate is a widely utilized excitatory neurotransmitter in mammalian brain. The ion channels activated by glutamate are typically divided into two classes.

General description N -methyl-d-aspartate receptor (NMDAR1) is a subtype of the ionotropic glutamate receptors (iGluRs). It is coded by GRIN1 gene.