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RUNX2 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement RUNX2 dans WB et IP. Il présente une réactivité envers Humain.
N° du produit ABIN7270117

Aperçu rapide pour RUNX2 anticorps (ABIN7270117)

Antigène

Voir toutes RUNX2 Anticorps
RUNX2 (Runt-Related Transcription Factor 2 (RUNX2))

Reactivité

  • 129
  • 53
  • 31
  • 10
  • 9
  • 8
  • 8
  • 8
  • 7
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 115
  • 19
Lapin

Clonalité

  • 107
  • 27
Monoclonal

Conjugué

  • 64
  • 10
  • 7
  • 6
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp RUNX2 est non-conjugé

Application

  • 102
  • 47
  • 37
  • 30
  • 19
  • 12
  • 10
  • 8
  • 7
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Fonction

    RUNX2 Rabbit mAb

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human RUNX2

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IP,1:50 - 1:200

    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

    RUNX2 (Runt-Related Transcription Factor 2 (RUNX2))

    Autre désignation

    RUNX2

    Sujet

    This gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Two regions of potential trinucleotide repeat expansions are present in the N-terminal region of the encoded protein, and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Jul 2016],AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD, OSF-2, OSF2, PEA2aA, PEBP2aA,Cell Biology & Developmental Biology,Epigenetics & Nuclear Signaling,Extracellular Matrix,Extracellular Matrix_Bone,Hippo Signaling Pathway,Mesenchymal Stem Cells,Stem Cells,TGF-b-Smad Signaling Pathway_Target gene,Transcription Factors,RUNX2

    Poids moléculaire

    kDa

    ID gène

    860

    UniProt

    Q13950
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