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Myosin 9 Antikörper (N-Term)

KO Validated MYH9 Reaktivität: Human WB, IF, IP, IHC (p), ICC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2855153
  • Target Alle Myosin 9 (MYH9) Antikörper anzeigen
    Myosin 9 (MYH9)
    Bindungsspezifität
    • 10
    • 9
    • 8
    • 7
    • 7
    • 7
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reaktivität
    • 84
    • 35
    • 32
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 71
    • 11
    • 2
    • 1
    • 1
    Kaninchen
    Klonalität
    • 72
    • 14
    Polyklonal
    Konjugat
    • 38
    • 9
    • 6
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 1
    Dieser Myosin 9 Antikörper ist unkonjugiert
    Applikation
    • 46
    • 43
    • 14
    • 13
    • 13
    • 9
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
    Spezifität
    This antibody may cross react with MYH10, MYH14, or other family members.
    Kreuzreaktivität
    Human
    Produktmerkmale
    Rabbit Polyclonal antibody to MYH9 (myosin, heavy chain 9, non-muscle)
    MYH9 antibody [N1], N-term
    Aufreinigung
    Purified by antigen-affinity chromatography.
    Güteklasse
    KO Validated
    Immunogen
    Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
    Isotyp
    IgG
    Top Product
    Discover our top product MYH9 Primärantikörper
  • Applikationshinweise
    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    Kommentare

    Positive Control: U87-MG , SK-N-SH , IMR32 , SK-N-AS , NT2D1 , PC-3

    Validation: KO/KD, Overexpression

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.31 mg/mL
    Buffer
    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target
    Myosin 9 (MYH9)
    Andere Bezeichnung
    myosin heavy chain 9 (MYH9 Produkte)
    Synonyme
    BDPLT6 antikoerper, DFNA17 antikoerper, EPSTS antikoerper, FTNS antikoerper, MHA antikoerper, NMHC-II-A antikoerper, NMMHC-IIA antikoerper, NMMHCA antikoerper, C80049 antikoerper, D0Jmb2 antikoerper, E030044M24Rik antikoerper, Fltn antikoerper, Myhn-1 antikoerper, Myhn1 antikoerper, NMHC II-A antikoerper, NMHCIIA antikoerper, NMMHC II-a antikoerper, NMMHC-A antikoerper, TU72.6 antikoerper, fi22c04 antikoerper, myh9 antikoerper, myh9l2 antikoerper, wu:fi22c04 antikoerper, wu:fj85e11 antikoerper, zgc:162029 antikoerper, zgc:66164 antikoerper, NMMHC antikoerper, myosin antikoerper, non-muscle antikoerper, nonmuscle antikoerper, KLG/PTK7 antikoerper, dfna17 antikoerper, epsts antikoerper, ftns antikoerper, nmhc-ii-a antikoerper, nmmhca antikoerper, myosin heavy chain 9 antikoerper, myosin, heavy polypeptide 9, non-muscle antikoerper, myosin, heavy chain 9a, non-muscle antikoerper, myosin, heavy chain 9, non-muscle antikoerper, myosin, heavy chain 9, non-muscle L homeolog antikoerper, MYH9 antikoerper, Myh9 antikoerper, myh9a antikoerper, myh9.L antikoerper
    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
    227 kDa
    Gen-ID
    4627
    UniProt
    P35579
    Pathways
    Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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