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Invitrogen™ NSDHL Recombinant Rabbit Monoclonal Antibody (24GB510)

Description
NSDHL Recombinant Monoclonal Antibody for Western Blot, ICC/IF, Flow
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 |
| Anwendungen | Flow Cytometry, Western Blot, Immunocytochemistry |
| Klassifikation | Recombinant Monoclonal |
| Klon | 24GB510 |
| Konjugat | Unconjugated |
| Zusammensetzung | PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 |
| Gen | Nsdhl |
| Gen-Zugriffsnummer | Q15738, Q5PPL3, Q9R1J0 |
| Gen-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 |
| Gensymbole | Nsdhl |
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Product Title
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