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NSDHL Antikörper

Der Kaninchen Polyklonal Anti-NSDHL-Antikörper wurde für WB validiert. Er ist geeignet, NSDHL in Proben von Human zu detektieren.
Produktnummer ABIN7465357

Kurzübersicht für NSDHL Antikörper (ABIN7465357)

Target

Alle NSDHL Antikörper anzeigen
NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

Reaktivität

  • 24
  • 7
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 20
  • 4
Kaninchen

Klonalität

  • 17
  • 7
Polyklonal

Konjugat

  • 20
  • 2
  • 1
  • 1
Dieser NSDHL Antikörper ist unkonjugiert

Applikation

  • 20
  • 12
  • 8
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Kreuzreaktivität

    Human

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

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

    Kommentare

    Positive Control: A431

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

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

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

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

    Andere Bezeichnung

    NAD(P) dependent steroid dehydrogenase-like

    Hintergrund

    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]

    Molekulargewicht

    42 kDa

    Gen-ID

    50814

    UniProt

    Q15738
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