NSDHL anticorps

N° du produit ABIN7465357

Détail du produit anti-NSDHL anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSDHL est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human NSDHL. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: A431

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur NSDHL

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

Autre désignation: NAD(P) dependent steroid dehydrogenase-like (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: NAD(P) dependent steroid dehydrogenase-like , H105E3 , SDR31E1 , XAP104,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]

Poids moléculaire: 42 kDa

ID gène: 50814

UniProt: Q15738