GM2/GD2 synthase Polyclonal Antibody, 20ul Buffer Solutions High consistency minimizes the inƍuence

High consistency minimizes the inƍuence of human operation on experimental outcomes

Mutations in the gene encoding CABC1 may be implicated in ubiquinone deficiency which can lead to cerebellar ataxia and seizures

and it plays a role in the regulation of inflammation

This gene has broad tissue distribution

CLEC4A (C-type lectin domain family 4 member A) encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily

GM2/GD2 synthase Polyclonal Antibody, 20ul Buffer Solutions High consistency minimizes the inƍuenceGM2 and GD2 gangliosides are sialic acid containing glycosphingolipids. Beta 1,4 N acetylgalactosaminyltransferase 1 is the enzyme involved in the biosynthesis of G(M2) and G(D2) glycosphingolipids. Beta 1,4 N acetylgalactosaminyltransferase 1 catalyzes the transfer of GalNAc into G(M3) and G(D3) by a beta 1,4 linkage, resulting in the synthesis of G(M2) and G(D2), respectively. Three transcript variants encoding different isoforms have been found for