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NT5C3 Polyclonal Antibody, 20ul Cellular Cultivation & Health Management This asymmetry in potassium ion

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NT5C3 Polyclonal Antibody, 20ul Cellular Cultivation & Health Management This asymmetry in potassium ionNT5C3A (5' nucleotidase, cytosolic IIIA) encodes a member of the 5' nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5' monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in NT5C3A are a cause of hemolytic anemia due to uridine 5 prime monophosphate hydrolase deficiency. Alternatively spliced transcript

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Description

This asymmetry in potassium ion conductance plays a key role in the excitability of muscle cells and neurons

Two alternatively spliced transcript variant encoding distinct isoforms have been reported

This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene

Pro-cathepsin H encoded by CTSH is a lysosomal cysteine proteinase important in the overall degradation of lysosomal proteins

NT5C3 Polyclonal Antibody, 20ul Cellular Cultivation & Health Management This asymmetry in potassium ionNT5C3A (5' nucleotidase, cytosolic IIIA) encodes a member of the 5' nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5' monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in NT5C3A are a cause of hemolytic anemia due to uridine 5 prime monophosphate hydrolase deficiency. Alternatively spliced transcript

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