STAC3 Polyclonal Antibody, 20ul Molecular Biology Mutations in this gene are

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

thereby influencing alternative transcript splicing

This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate

Inhibition is achieved by formation of an equimolar

INCENP (inner centromere protein) and survivin

STAC3 Polyclonal Antibody, 20ul Molecular Biology Mutations in this gene areThe protein encoded by this gene is a component of the excitation contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N terminal cysteine rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy.