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T-Box 1 Antikörper

Der Kaninchen Polyklonal Anti-T-Box 1-Antikörper wurde für WB, ELISA und IHC validiert. Er ist geeignet, T-Box 1 in Proben von Human zu detektieren.
Produktnummer ABIN7254388

Kurzübersicht für T-Box 1 Antikörper (ABIN7254388)

Target

Alle T-Box 1 (TBX1) Antikörper anzeigen
T-Box 1 (TBX1)

Reaktivität

  • 53
  • 21
  • 20
  • 4
  • 4
  • 2
  • 1
Human

Wirt

  • 51
  • 2
  • 1
Kaninchen

Klonalität

  • 52
  • 2
Polyklonal

Konjugat

  • 23
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser T-Box 1 Antikörper ist unkonjugiert

Applikation

  • 42
  • 18
  • 15
  • 14
  • 14
  • 6
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human TBX1

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.7 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    T-Box 1 (TBX1)

    Andere Bezeichnung

    TBX1

    Hintergrund

    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. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.

    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 43 kDa

    UniProt

    O43435

    Pathways

    Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation
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