NSDHL anticorps

N° du produit ABIN2463049

Détail du produit anti-NSDHL anticorps

Antigène: NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSDHL est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by protein A chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSDHL.

Information d'application

Indications d'application: 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.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSDHL antibody at -20 °C.

Détails sur NSDHL

Antigène: NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

Autre désignation: NSDHL (NSDHL Produits)

Synonymes: anticorps zgc:112474, anticorps H105E3, anticorps SDR31E1, anticorps XAP104, anticorps AI747449, anticorps Bpa, anticorps Str, anticorps NAD(P) dependent steroid dehydrogenase-like, anticorps NAD(P) dependent steroid dehydrogenase-like L homeolog, anticorps NSDHL, anticorps nsdhl, anticorps nsdhl.L, anticorps Nsdhl

Sujet: 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.

Poids moléculaire: 42 kDa

ID gène: 50814

NCBI Accession: NP_057006

UniProt: Q15738