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T-Box 19 Antikörper

Der Kaninchen Polyklonal Anti-T-Box 19-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, T-Box 19 in Proben von Human zu detektieren.
Produktnummer ABIN7466038

Kurzübersicht für T-Box 19 Antikörper (ABIN7466038)

Target

Alle T-Box 19 (TBX19) Antikörper anzeigen
T-Box 19 (TBX19)

Reaktivität

  • 11
  • 8
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 11
  • 1
Kaninchen

Klonalität

  • 9
  • 3
Polyklonal

Konjugat

  • 12
Dieser T-Box 19 Antikörper ist unkonjugiert

Applikation

  • 12
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Kreuzreaktivität

    Human

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human TBX19. The exact sequence is proprietary.

    Isotyp

    IgG
  • Applikationshinweise

    WB: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Kommentare

    Positive Control: HepG2

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % 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

    T-Box 19 (TBX19)

    Andere Bezeichnung

    T-box 19

    Hintergrund

    T-box 19 , TBS19 , TPIT , dJ747L4.1,This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq]

    Molekulargewicht

    48 kDa

    Gen-ID

    9095

    UniProt

    O60806
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