NSDHL Antikörper
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- Target Alle NSDHL Antikörper anzeigen
- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
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Reaktivität
- Human, Ratte, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser NSDHL Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA
- Aufreinigung
- Antibody is purified by protein A chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSDHL.
- Top Product
- Discover our top product NSDHL Primärantikörper
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- Applikationshinweise
- NSDHL antibody can be used for detection of NSDHL by ELISA at 1:312500. NSDHL antibody can be used for detection of NSDHL by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Konzentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handhabung
- As with any antibody avoid repeat freeze-thaw cycles.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSDHL antibody at -20 °C.
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- Target
- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
- Andere Bezeichnung
- NSDHL (NSDHL Produkte)
- Synonyme
- zgc:112474 antikoerper, H105E3 antikoerper, SDR31E1 antikoerper, XAP104 antikoerper, AI747449 antikoerper, Bpa antikoerper, Str antikoerper, NAD(P) dependent steroid dehydrogenase-like antikoerper, NAD(P) dependent steroid dehydrogenase-like L homeolog antikoerper, NSDHL antikoerper, nsdhl antikoerper, nsdhl.L antikoerper, Nsdhl antikoerper
- Hintergrund
- NSDHL is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in NSDHL 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.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.
- Molekulargewicht
- 42 kDa
- Gen-ID
- 50814
- NCBI Accession
- NP_057006
- UniProt
- Q15738
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