分子量：Calculated MW: 41kDa
Observed MW: Refer to figures

稀釋方法：WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50 - 1:200

總結：The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.