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Dystrophin Antikörper (AA 114-263)

Der Maus Monoklonal anti-Dystrophin Antikörper wird verwendet zum Nachweis von Dystrophin in Proben von Human. Er wurde validiert für IHC und ELISA.
Produktnummer ABIN6937095
639,45 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 10 Werktagen

Kurzübersicht für Dystrophin Antikörper (AA 114-263) (ABIN6937095)

Target

Alle Dystrophin (DMD) Antikörper anzeigen
Dystrophin (DMD)

Reaktivität

  • 112
  • 18
  • 17
  • 3
  • 2
Human

Wirt

  • 74
  • 39
Maus

Klonalität

  • 88
  • 25
Monoklonal

Konjugat

  • 68
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Dystrophin Antikörper ist unkonjugiert

Applikation

  • 56
  • 32
  • 29
  • 28
  • 26
  • 12
  • 10
  • 8
  • 4
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA

Klon

DMD-3245
  • Bindungsspezifität

    • 55
    • 8
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 114-263

    Verwendungszweck

    Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Antibody

    Spezifität

    Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002 % of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Kreuzreaktivität (Details)

    Human.

    Aufreinigung

    200ug/ml of Ab Purified from Bioreactor Concentrate by Protein A/G.

    Immunogen

    A recombinant fragment (around aa 114-263) of human DMD protein (exact sequence is proprietary)

    Isotyp

    IgG2a, kappa
  • Applikationshinweise

    Known_Application: ELISA (For coating, order Ab without BSA),Immunohistochemistry (Formalin-fixed) (1-2 μg/mL for 30 minutes at RT),(Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 min at 95°C followed by cooling at RT for 20 minutes), Optimal dilution for a specific application should be determined.

    Positive_Control: Human skeletal muscle and heart muscle tissues (IHC).

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1.0 mg/mL

    Buffer

    Prepared in 10  mM PBS

    Konservierungsmittel

    Azide free

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.

    Haltbarkeit

    24 months
  • Target

    Dystrophin (DMD)

    Andere Bezeichnung

    DMD

    Hintergrund

    BMD, CMD3B, Duchenne muscular dystrophy (DMD), Dystrophin, Muscular dystrophy Duchenne and Becker types

    Human skeletal muscle and heart muscle tissues (IHC).

    Molekulargewicht

    427kDa

    Gen-ID

    1756, 495912

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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