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DLX3 Antikörper

Der Kaninchen Monoklonal Anti-DLX3-Antikörper wurde für WB validiert. Er ist geeignet, DLX3 in Proben von Human zu detektieren.
Produktnummer ABIN7266800

Kurzübersicht für DLX3 Antikörper (ABIN7266800)

Target

Alle DLX3 Antikörper anzeigen
DLX3 (Distal-Less Homeobox 3 (DLX3))

Reaktivität

  • 33
  • 23
  • 10
  • 9
  • 8
  • 7
  • 7
  • 6
  • 6
  • 6
  • 3
  • 2
  • 2
  • 1
Human

Wirt

  • 29
  • 4
Kaninchen

Klonalität

  • 29
  • 4
Monoklonal

Konjugat

  • 26
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DLX3 Antikörper ist unkonjugiert

Applikation

  • 25
  • 12
  • 12
  • 4
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    DLX3 Rabbit mAb

    Kreuzreaktivität

    Human, Maus

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of Human DLX3.

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    DLX3 (Distal-Less Homeobox 3 (DLX3))

    Andere Bezeichnung

    DLX3

    Hintergrund

    Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.,DLX3,AI4,TDO,Epigenetics & Nuclear Signaling,Transcription Factors,DLX3

    Molekulargewicht

    31kDa

    Gen-ID

    1747

    UniProt

    O60479
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