NSDHL Rabbit anti-Human, Polyclonal, Bioss
Rabbit Polyclonal Antibody
Manufacturer: Bioss BS5088R
DescriptionThe 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 ft. UTR have been found for this gene.
|Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot|
|PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH|
|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|
|KLH conjugated synthetic peptide derived from human NSDHL.|
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