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Runt-Related Transcription Factor 2 (RUNX2) (N-Term) Peptide

RUNX2 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN983332

Quick Overview for Runt-Related Transcription Factor 2 (RUNX2) (N-Term) Peptide (ABIN983332)

Target

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

Origin

Human

Source

  • 8
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Sequence

    MRIPVDPSTS RRFSPPSSSL QPGKMSDVSP VVAAQQQQQQ QQQQQQQQQQ

    Characteristics

    This is a synthetic peptide designed for use in combination with anti-RUNX2 Antibody(ARP38452_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

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

    Background

    RUNX2 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, acting 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. Mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants, encoding different protein isoforms, result from alternate promoter use as well as alternate splicing.

    Alias Symbols: AML3, CBFA1, CCD, CCD1, MGC120022, MGC120023, OSF2, PEA2aA, PEBP2A1, PEBP2A2, PEBP2aA, PEBP2aA1, OSF-2

    Protein Interaction Partner: RB1,AR,AXIN1,CBFB,CCNB1,CDK1,CEBPB,DVL2,EP300,ETS1,FOS,HDAC3,HDAC4,HDAC6,JUN,LEF1,MAP3K4,MSX2,MYST4,PRKCD,RB1,SMAD2,SMAD3,SMAD6,TAF1A,UBTF,XRCC5,XRCC6,YAP1,BMPR1A,EP300,ETS1,FOS,HDAC1,HDAC3,HDAC4,HDAC5,HDAC6,HES1,JUN,KAT2B,LEF1,MSX2,MYST4,SMAD1,SMAD2,SMAD

    Protein Size: 507

    Molecular Weight

    55 kDa

    Gene ID

    860

    NCBI Accession

    NM_004348, NP_004339
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