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Dystrophin anticorps (AA 1700-2300)

Cet anticorps anti-Dystrophin Monoclonal Souris (Clone DMD-6270) (ABIN7862711) détecte spécifiquement Dystrophin dans IHC. L’anticorps est réactif avec des échantillons de Humain et Chien.
N° du produit ABIN7862711
639,45 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 6 à 10 jours ouvrables

Aperçu rapide pour Dystrophin anticorps (AA 1700-2300) (ABIN7862711)

Antigène

Voir toutes Dystrophin (DMD) Anticorps
Dystrophin (DMD)

Reactivité

  • 112
  • 18
  • 17
  • 3
  • 1
Humain, Chien

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
  • 30
  • 28
  • 26
  • 12
  • 10
  • 8
  • 4
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC)

Clone

DMD-6270
  • Épitope

    • 56
    • 7
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1700-2300

    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.

    Purification

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

    Immunogène

    Recombinant fragment (around aa1700-2300) of human DMD (exact sequence is proprietary).

    Isotype

    IgG2a, kappa
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Prepared in 10 mM PBS with 0.05 % BSA & 0.05 % azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °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

    Dystrophin

    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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