NSDHL 抗体
(NAD(P) Dependent Steroid Dehydrogenase-Like (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. [provided by RefSeq, Jul 2008].
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25 results
NSDHL
适用: 人
WB, ELISA, IHC
宿主: 兔
Monoclonal
20F2
unconjugated
Recombinant Antibody
Latest Publications for our NSDHL 抗体
: "Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells." in: Nature methods, Vol. 10, Issue 4, pp. 315-23, (2013) (PubMed).: "Intercellular transfer of proteins as identified by stable isotope labeling of amino acids in cell culture." in: The Journal of biological chemistry, Vol. 285, Issue 9, pp. 6285-97, (2010) (PubMed).
: "Proteomic analysis of enriched lysosomes at early phase of camptothecin-induced apoptosis in human U-937 cells." in: Journal of proteomics, Vol. 72, Issue 6, pp. 960-73, (2009) (PubMed).
Aliases for NSDHL 抗体
NAD(P) dependent steroid dehydrogenase-like (NSDHL) 抗体NAD(P) dependent steroid dehydrogenase-like (nsdhl) 抗体
NAD(P) dependent steroid dehydrogenase-like L homeolog (nsdhl.L) 抗体
NAD(P) dependent steroid dehydrogenase-like (Nsdhl) 抗体
AI747449 抗体
Bpa 抗体
H105E3 抗体
SDR31E1 抗体
Str 抗体
XAP104 抗体
zgc:112474 抗体
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