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RUNX2 antibody

This Rabbit Monoclonal antibody specifically detects RUNX2 in WB and IP. It exhibits reactivity toward Human.
Catalog No. ABIN7270117

Quick Overview for RUNX2 antibody (ABIN7270117)

Target

See all RUNX2 Antibodies
RUNX2 (Runt-Related Transcription Factor 2 (RUNX2))

Reactivity

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

Host

  • 122
  • 13
Rabbit

Clonality

  • 114
  • 21
Monoclonal

Conjugate

  • 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
This RUNX2 antibody is un-conjugated

Application

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

    RUNX2 Rabbit mAb

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human RUNX2

    Isotype

    IgG
  • Application Notes

    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.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

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

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

    Alternative Name

    RUNX2

    Background

    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

    Molecular Weight

    kDa

    Gene ID

    860

    UniProt

    Q13950
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