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RUNX2 Antikörper

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch RUNX2 in WB und IP. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7270117

Kurzübersicht für RUNX2 Antikörper (ABIN7270117)

Target

Alle RUNX2 Antikörper anzeigen
RUNX2 (Runt-Related Transcription Factor 2 (RUNX2))

Reaktivität

  • 127
  • 58
  • 33
  • 10
  • 9
  • 8
  • 8
  • 8
  • 7
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 122
  • 13
Kaninchen

Klonalität

  • 114
  • 21
Monoklonal

Konjugat

  • 70
  • 9
  • 6
  • 6
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser RUNX2 Antikörper ist unkonjugiert

Applikation

  • 103
  • 50
  • 35
  • 31
  • 15
  • 14
  • 12
  • 10
  • 7
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Verwendungszweck

    RUNX2 Rabbit mAb

    Kreuzreaktivität

    Human, Maus

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human RUNX2

    Isotyp

    IgG
  • Applikationshinweise

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

    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

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

    Andere Bezeichnung

    RUNX2

    Hintergrund

    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

    Molekulargewicht

    kDa

    Gen-ID

    860

    UniProt

    Q13950
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