B4GN2 Polyclonal Antibody, 100ul PCR Series Defects in SIX1 are a

Defects in SIX1 are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3)

a single membrane-spanning region

This component is a heteromeric complex consisting of three catalytic subunits encoded by mitochondrial genes

Each pouch contains 1L of concentrated solution

CYSLTR1 encodes a member of the G-protein coupled receptor 1 family

B4GN2 Polyclonal Antibody, 100ul PCR Series Defects in SIX1 are aB4GALNT2 catalyzes the last step in the biosynthesis of the human Sd(a) antigen through the addition of an N acetylgalactosamine residue via a beta 1,4 linkage to a subterminal galactose residue substituted with an alpha 2,3 linked sialic acid. B4GALNT2 also catalyzes the last step in the biosynthesis of the Cad antigen (Montiel et al., 2003