MAN1B1 Polyclonal Antibody, 50ul Glassware Sets the Ca(2+) that entered across

the Ca(2+) that entered across the sarcolemma must be extruded from the cell

At least three transcript variants encoding different isoforms have been found for this gene

This gene has a polymorphism at codon 54 that identified an alanine-encoding allele and a threonine-encoding allele

This gene is a candidate gene for Hirschsprung disease

MAN1B1 Polyclonal Antibody, 50ul Glassware Sets the Ca(2+) that entered acrossMAN1B1 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