CLC10 Polyclonal Antibody, 50ul Glassware Sets Defects in this gene cause

Defects in this gene cause congenital erythropoietic porphyria (Gunther's disease)

smooth and transparent tube body with clear graduation

The extracellular domains interact in a homophilic manner to specify differential cell-cell connections

Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases

CLC10 Polyclonal Antibody, 50ul Glassware Sets Defects in this gene causeThis gene encodes a member of the C type lectin C type lectin like domain (CTL CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell surface antigen. Two transcript variants encoding distinct isoforms have been identified for this