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Dystrophin anticorps (AA 114-263)

L’anticorps anti-Dystrophin Monoclonal Souris est utilisé pour la détection de Dystrophin dans des échantillons de Humain. Il a été validé pour IHC et ELISA.
N° du produit ABIN6937092
639,45 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 10 jours ouvrables

Aperçu rapide pour Dystrophin anticorps (AA 114-263) (ABIN6937092)

Antigène

Voir toutes Dystrophin (DMD) Anticorps
Dystrophin (DMD)

Reactivité

  • 112
  • 18
  • 17
  • 3
  • 2
Humain

Hôte

  • 74
  • 39
Souris

Clonalité

  • 88
  • 25
Monoclonal

Conjugué

  • 68
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Dystrophin est non-conjugé

Application

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

Clone

DMD-3242
  • Épitope

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

    Fonction

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

    Specificité

    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.

    Réactivité croisée (Details)

    Human.

    Purification

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

    Immunogène

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

    Isotype

    IgG2b, kappa
  • Indications d'application

    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).

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    Prepared in 10  mM PBS

    Agent conservateur

    Azide free

    Stock

    -20 °C,-80 °C

    Stockage commentaire

    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.

    Date de péremption

    24 months
  • Antigène

    Dystrophin (DMD)

    Autre désignation

    DMD

    Sujet

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

    Human skeletal muscle and heart muscle tissues (IHC).

    Poids moléculaire

    427kDa

    ID gène

    1756, 495912

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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