MAN1B1 Polyclonal Antibody, 20ul 3D Culture Mutations in this gene have

Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM)

reducing the risk of contamination during handling

This enzyme catalyzes the hydrolysis of a terminal beta-linked galactose residue from ganglioside substrates and other glycoconjugates

CGB3 is a member of the glycoprotein hormone beta chain family and encodes the beta 3 subunit of chorionic gonadotropin (CG)

Keratin 18

MAN1B1 Polyclonal Antibody, 20ul 3D Culture Mutations in this gene haveMAN1B1 encodes an enzyme belonging to the glycosyl hydrolase 47 family. This enzyme functions in N glycan biosynthesis, and is a class I alpha 1,2 mannosidase that specifically converts Man9GlcNAc to Man8GlcNAc isomer B. It is required for N glycan trimming to Man5 6GlcNAc2 in the endoplasmic reticulum associated degradation pathway. Mutations in this gene cause autosomal recessive intellectual disability. Alternative splicing results in multiple