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Myosin 9 Antikörper (N-Term)

MYH9 Reaktivität: Human, Maus WB, FACS Wirt: Kaninchen Polyclonal RB36361 unconjugated
Produktnummer ABIN6243267
  • Target Alle Myosin 9 (MYH9) Antikörper anzeigen
    Myosin 9 (MYH9)
    Bindungsspezifität
    • 8
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 134-165, N-Term
    Reaktivität
    • 57
    • 13
    • 11
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 44
    • 11
    • 2
    • 1
    • 1
    Kaninchen
    Klonalität
    • 44
    • 15
    Polyklonal
    Konjugat
    • 39
    • 5
    • 5
    • 5
    • 2
    • 2
    • 1
    Dieser Myosin 9 Antikörper ist unkonjugiert
    Applikation
    • 45
    • 36
    • 16
    • 14
    • 11
    • 9
    • 8
    • 6
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS)
    Homologie
    C, Rat
    Aufreinigung
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 134-165 amino acids from the N-terminal region of human MYH9.
    Klon
    RB36361
    Isotyp
    Ig Fraction
    Top Product
    Discover our top product MYH9 Primärantikörper
  • Applikationshinweise
    WB: 1:1000. WB: 1:1000. FC: 1:10~50
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Haltbarkeit
    6 months
  • Target
    Myosin 9 (MYH9)
    Andere Bezeichnung
    MYH9 (MYH9 Produkte)
    Hintergrund
    This gene encodes 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
    226532
    NCBI Accession
    NP_002464
    UniProt
    P35579
    Pathways
    Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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