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SMR3B Rabbit Polyclonal Antibody, 50ul PCR Series Mutations in NT5C3A are a

SKU: 12296616122

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SMR3B Rabbit Polyclonal Antibody, 50ul PCR Series Mutations in NT5C3A are a

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Description

Mutations in NT5C3A are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency

It is responsible for decreased drug accumulation in multidrug-resistant cells and often mediates the development of resistance to anticancer drugs

This protein (activating transcription factor 1) is phosphorylated at serine 63 in its kinase-inducible domain by serine/threonine kinases

but are not absent of

Each domain contains two cysteines

SMR3B Rabbit Polyclonal Antibody, 50ul PCR Series Mutations in NT5C3A are a

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