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SRY (Sex Determining Region Y)-Box 9 (SOX9) Peptide

SOX9 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN984285
  • Target See all SOX9 products
    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
    Origin
    Human
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-SOX9 antibody (Catalog #: P100797_T100). 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
    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
    Synonyms
    CMD1 Peptide, CMPD1 Peptide, SRA1 Peptide, LOC100227849 Peptide, 2010306G03Rik Peptide, AV220920 Peptide, mKIAA4243 Peptide, SOX-9 Peptide, cmd1 Peptide, cmpd1 Peptide, sox-9 Peptide, sox9 Peptide, sox9-a Peptide, sox9-b Peptide, sox9b Peptide, sra1 Peptide, SRY-box 9 Peptide, transcription factor SOX-9 Peptide, SRY (sex determining region Y)-box 9 Peptide, SRY box 9 Peptide, SRY-box 9 L homeolog Peptide, SOX9 Peptide, LOC100227849 Peptide, Sox9 Peptide, sox9.L Peptide
    Background
    SOX9 recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal.

    Alias Symbols: CMD1, SRA1, CMPD1

    Protein Interaction Partner: KPNB1,CREB1,CREBBP,EP300,HSPA1A,KPNB1,MAF,MED12,NR5A1,SPEN,TRAF2,HSPA1A,MAF,MED12,NR5A1

    Protein Size: 509
    Molecular Weight
    56 kDa
    Gene ID
    6662
    NCBI Accession
    NM_000346, NP_000337
    UniProt
    P48436
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