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GAPDH Polyclonal Antibody, 50ul[BT-AP15693] Antibody Development Mutations in CACNA2D1 can cause

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GAPDH Polyclonal Antibody, 50ul[BT-AP15693] Antibody Development Mutations in CACNA2D1 can causeThis gene encodes a member of the glyceraldehyde 3 phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde 3 phosphate in the presence of inorganic phosphate and nicotinamide

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Description

Mutations in CACNA2D1 can cause cardiac deficiencies

APOL5 (apolipoprotein L5) is a member of the apolipoprotein L gene family

Arg-19 and Arg-25 are dimethylated

This gene encodes a member of the synuclein family of proteins which are believed to be involved in the pathogenesis of neurodegenerative diseases

from prostatic intraepithelial neoplasia to invasive prostate cancer

GAPDH Polyclonal Antibody, 50ul[BT-AP15693] Antibody Development Mutations in CACNA2D1 can causeThis gene encodes a member of the glyceraldehyde 3 phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde 3 phosphate in the presence of inorganic phosphate and nicotinamide

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