NSDHL antibody

GeneTex

NSDHL antibody

9

Research Use Only

1 mg/ml

IgG

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. [provided by RefSeq]

2°C to 8°C,-20°C

12352203