Sox2(Phospho-Ser250/Ser251) Rabbit Polyclonal Antibody, 20ul Lysosome Mutations in this gene have

Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency

This gene belongs to the ubiquitin C-terminal hydrolase subfamily of deubiquitinating enzymes that are involved in the removal of ubiquitin from proteins

also known as BDPL or lens BTB domain protein

Alternative promoter usage and splicing of this gene leads to two different isoforms: the mitochondrial UNG1 and the nuclear UNG2

as well as cross-contamination

Sox2(Phospho-Ser250/Ser251) Rabbit Polyclonal Antibody, 20ul Lysosome Mutations in this gene haveThis 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