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K1644 Rabbit Polyclonal Antibody, 50ul Mechanical Pipette Mutations in this gene are

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K1644 Rabbit Polyclonal Antibody, 50ul Mechanical Pipette Mutations in this gene are

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Description

Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens

These molecules participate in a broad range of cellular functions which include cell cycle modulation| scavenging reactive oxygen species| and the control of gene expression

In M phase

The encoded protein homodimerizes and functions as an outwardly rectifying channel

A pseudogene has been identified on chromosome 21

K1644 Rabbit Polyclonal Antibody, 50ul Mechanical Pipette Mutations in this gene are

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