SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in this gene cause

Mutations in this gene cause Joubert syndrome

Each beta4GalT member has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures

a complex that acts as a key regulator of mitosis

Diseases associated with PRAF2 include neuroblastoma

which was initially cloned from human dermal papilla cells and is evolutionally conserved from drosophila through to humans

SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in this gene causeThe protein encoded by this gene is an epithelial brush border Na H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22.