Sox2(Phospho-Ser250/Ser251) Rabbit Polyclonal Antibody, 100ul Molecular Weight Markers diclofenac

diclofenac

Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I

which are located in its third and fifth introns

This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer

Sox2(Phospho-Ser250/Ser251) Rabbit Polyclonal Antibody, 100ul Molecular Weight Markers diclofenacThis intronless gene encodes a member of the SRY related HMG box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem cell maintenance in the central nervous system and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia a severe