missing translation for 'onlineSavingsMsg'
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Invitrogen™ NSDHL Polyclonal Antibody

Description
Antibody detects endogenous levels of total NSDHL.
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.
Specifications
Specifications
| Antigen | NSDHL |
| Applications | Immunohistochemistry (Paraffin), Western Blot |
| Classification | Polyclonal |
| Concentration | 1 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 |
| Gene | Nsdhl |
| Gene Accession No. | Q15738, Q5PPL3, Q9R1J0 |
| Gene Alias | AI747449; bare patches; Bpa; H105E3; NAD(P) dependent steroid dehydrogenase-like; NAD(P)-dependent steroid dehydrogenase-like protein; Nsdhl; Protein H105e3; SDR31E1; short chain dehydrogenase/reductase family 31E, member 1; sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating; Str; striated; XAP104 |
| Gene Symbols | Nsdhl |
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