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Myosin 9 (MYH9) Peptid

MYH9 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN937246

Kurzübersicht für Myosin 9 (MYH9) Peptid (ABIN937246)

Target

Myosin 9 (MYH9)

Spezies

Säugetier

Quelle

  • 4
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    DAMNREVSSL KNKLRRGDLP FVVPRRMARK GAGDGSDEEV DGKADGAEAK

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of MYH9 antibody,
    Alternative Names: MYH9 control peptide, MYH9 antibody Blocking Peptide, Anti-MYH9 Blocking Peptide, Myosin Heavy Chain 9 Non-Muscle Blocking Peptide, DFNA17 Blocking Peptide, EPSTS Blocking Peptide, FTNS Blocking Peptide, MGC104539 Blocking Peptide, MHA Blocking Peptide, NMHC-II-A Blocking Peptide, NMMHCA Blocking Peptide, MYH9, MYH-9, MYH 9, MYH-9 Blocking Peptide, MYH 9 Blocking Peptide

    Aufreinigung

    Rabbit Anti-EGFR (Phospho-Tyr1197) Polyclonal Antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide is removed by chromatogramphy using non-phosphopeptide corresponding to the phosphorylation site.
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

    Myosin 9 (MYH9)

    Hintergrund

    MYH9 is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

    Molekulargewicht

    226 kDa
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