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Myosin 9 (MYH9) Peptide

MYH9 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN937246

Aperçu rapide pour Myosin 9 (MYH9) Peptide (ABIN937246)

Antigène

Myosin 9 (MYH9)

Origine

Mammifères

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    DAMNREVSSL KNKLRRGDLP FVVPRRMARK GAGDGSDEEV DGKADGAEAK

    Attributs du produit

    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

    Purification

    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.
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    Myosin 9 (MYH9)

    Sujet

    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.

    Poids moléculaire

    226 kDa
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