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Dystrophin anticorps (AA 114-263)

L’anticorps Souris Monoclonal anti-Dystrophin a été validé pour IHC, ELISA, Coat et IHC (f). Il convient pour détecter Dystrophin dans des échantillons de Humain.
N° du produit ABIN6937092

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

Antigène

Voir toutes Dystrophin (DMD) Anticorps
Dystrophin (DMD)

Reactivité

  • 79
  • 17
  • 16
  • 3
Humain

Hôte

  • 47
  • 33
Souris

Clonalité

  • 56
  • 24
Monoclonal

Conjugué

  • 35
  • 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

  • 50
  • 28
  • 26
  • 14
  • 10
  • 8
  • 7
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA, Coating (Coat), Immunohistochemistry (Formalin-fixed Sections) (IHC (f))

Clone

DMD-3242
  • Épitope

    • 31
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 114-263

    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

    1.0mg/ml of Ab purified from Bioreactor 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, WITHOUT BSA and Azide.

    Agent conservateur

    Azide free

    Stock

    -20 °C,-80 °C

    Stockage commentaire

    Antibody without azide store at -20 to -80 °C. Antibody is stable for 24 months. Non-hazardous.

    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,Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy)
    Cellular localisation: Cell Surface and Cytoplasmic

    Poids moléculaire

    427kDa

    ID gène

    1756, 495912

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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