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IHC-P analysis of mouse embryo tissue using GTX37759 RUNX2 antibody.
IHC-P analysis of mouse embryo tissue using GTX37759 RUNX2 antibody.
IHC-P analysis of mouse embryo tissue using GTX37759 RUNX2 antibody.

RUNX2 antibody

GTX37759
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetRUNX2
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Overview

  • Supplier
    GeneTex
  • Product Name
    RUNX2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:400-800. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID860
  • Target name
    RUNX2
  • Target description
    RUNX family transcription factor 2
  • Target synonyms
    acute myeloid leukemia 3 protein; AML3; CBFA1; CBF-alpha-1; CCD; CCD1; CLCD; core-binding factor, runt domain, alpha subunit 1; oncogene AML-3; OSF2; OSF-2; osteoblast-specific transcription factor 2; PEA2aA; PEA2-alpha A; PEBP2aA; PEBP2-alpha A; polyomavirus enhancer-binding protein 2 alpha A subunit; runt related transcription factor 2; runt-related transcription factor 2; SL3/AKV core-binding factor alpha A subunit; SL3-3 enhancer factor 1 alpha A subunit
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ13950
  • Protein Name
    Runt-related transcription factor 2
  • Scientific Description
    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]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203