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DLX3 anticorps

L’anticorps Lapin Monoclonal anti-DLX3 a été validé pour WB. Il convient pour détecter DLX3 dans des échantillons de Humain.
N° du produit ABIN7266800

Aperçu rapide pour DLX3 anticorps (ABIN7266800)

Antigène

Voir toutes DLX3 Anticorps
DLX3 (Distal-Less Homeobox 3 (DLX3))

Reactivité

  • 31
  • 22
  • 10
  • 9
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  • 7
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  • 3
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  • 1
Humain

Hôte

  • 27
  • 4
Lapin

Clonalité

  • 28
  • 3
Monoclonal

Conjugué

  • 24
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DLX3 est non-conjugé

Application

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Western Blotting (WB)
  • Fonction

    DLX3 Rabbit mAb

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of Human DLX3.

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    DLX3 (Distal-Less Homeobox 3 (DLX3))

    Autre désignation

    DLX3

    Sujet

    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

    Poids moléculaire

    31kDa

    ID gène

    1747

    UniProt

    O60479
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