Anti-NSDHL Polyclonal Antibody, 100.0ul

£243.06
Delivery: 2 weeks
SKU
K109317P-100.0ul
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.

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.

  • Size: 100.0ul
  • Molecular Weight: 42kDa
  • Physical State: Liquid
  • Storage: Store at -20℃. Avoid freeze/thaw cycles.
  • Application: WB;IHC
  • Brand: Saint Michael
  • Catalogue No.: K109317P-100.0ul

For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.

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