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Septin 9 (SEPT9) (Middle Region) Peptide

SEPT9 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN983544
  • Target See all Septin 9 (SEPT9) products
    Septin 9 (SEPT9)
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    VNEKFREMIP FAVVGSDHEY QVNGKRILGR KTKWGTIEVE NTTHCEFAYL
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-SEPT9 Antibody(ARP51756_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
    Septin 9 (SEPT9)
    Synonyms
    SEPT9 Peptide, msf Peptide, msf1 Peptide, napb Peptide, sint1 Peptide, pnutl4 Peptide, septd1 Peptide, af17q25 Peptide, septin-9 Peptide, AF17q25 Peptide, MSF Peptide, MSF1 Peptide, NAPB Peptide, PNUTL4 Peptide, SINT1 Peptide, SeptD1 Peptide, Msf Peptide, Sint1 Peptide, Eseptin Peptide, Slpa Peptide, cb999 Peptide, fb02h06 Peptide, sept9 Peptide, wu:fb02h06 Peptide, septin 9 Peptide, septin-9 Peptide, septin 9 S homeolog Peptide, septin 9a Peptide, SEPT9 Peptide, sept9 Peptide, LOC100605286 Peptide, sept9.S Peptide, Sept9 Peptide, sept9a Peptide
    Background
    This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.

    Alias Symbols: AF17q25, KIAA0991, MSF, MSF1, NAPB, PNUTL4, SINT1, SeptD1

    Protein Interaction Partner: HIF1A,RAB10,SEPT11,SEPT2,SEPT6,SEPT7,DDA1,HIF1A,IKBKG,SEPT2,SEPT6,SEPT7,SRRM2

    Protein Size: 422
    Molecular Weight
    46 kDa
    Gene ID
    10801
    NCBI Accession
    NM_001113492, NP_001106964
    UniProt
    Q9UHD8
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