MAN1B1 Polyclonal Antibody, 20ul 3D Culture reducing the risk of contamination

reducing the risk of contamination during handling

The Fanconi anemia complementation group (FANC) currently includes FANCA

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

smooth muscle

MAN1B1 Polyclonal Antibody, 20ul 3D Culture reducing the risk of contaminationMAN1B1 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