MAT2B Rabbit Polyclonal Antibody, 20ul Bottles Mutations in this gene are

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

The protein is essential for intestinal chloride absorption

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Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1

NMDAR2C (GRIN2C)

MAT2B Rabbit Polyclonal Antibody, 20ul Bottles Mutations in this gene areThe protein encoded by this gene belongs to the methionine adenosyltransferase (MAT) family. MAT catalyzes the biosynthesis of S adenosylmethionine from methionine and ATP. This protein is the regulatory beta subunit of MAT. Alternative splicing results in multiple transcript variants encoding different isoforms.