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MAN1B1 Polyclonal Antibody, 20ul 3D Culture This enzyme catalyzes the hydrolysis

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MAN1B1 Polyclonal Antibody, 20ul 3D Culture This enzyme catalyzes the hydrolysisMAN1B1 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

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Description

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

CGGBP1 (CGG triplet repeat binding protein 1) influences expression of the FMR1 gene (MIM 309550)

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

This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ)

Low-density lipoprotein receptor class A domain-containing protein 1 encoded by LDLRAD1 is a low-density lipoprotein receptor

MAN1B1 Polyclonal Antibody, 20ul 3D Culture This enzyme catalyzes the hydrolysisMAN1B1 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

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