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Dystrophin anticorps (AA 3076-3404)

L’anticorps anti-Dystrophin Polyclonal Lapin est utilisé pour la détection de Dystrophin dans des échantillons de Humain, Souris et Rat. Il a été validé pour IHC, WB, ICC, FACS et IHC (fro).
N° du produit ABIN7986733
500,50 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour Dystrophin anticorps (AA 3076-3404) (ABIN7986733)

Antigène

Voir toutes Dystrophin (DMD) Anticorps
Dystrophin (DMD)

Reactivité

  • 123
  • 28
  • 27
  • 3
  • 2
Humain, Souris, Rat

Hôte

  • 75
  • 49
Lapin

Clonalité

  • 89
  • 35
Polyclonal

Conjugué

  • 69
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Dystrophin est non-conjugé

Application

  • 59
  • 34
  • 32
  • 28
  • 26
  • 12
  • 12
  • 10
  • 8
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), Western Blotting (WB), Immunocytochemistry (ICC), Flow Cytometry (FACS), Immunohistochemistry (Frozen Sections) (IHC (fro))

Classe de qualité

Carrier-free
  • Épitope

    • 56
    • 11
    • 8
    • 6
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 3076-3404

    Fonction

    Anti-Dystrophin/DMD Antibody

    Specificité

    No cross reactivity with other proteins.

    Réactivité croisée (Details)

    No cross-reactivity with other proteins

    Homologie

    Human Dystrophin shares 100% amino acid (aa) sequence identity with mouse Dystrophin.

    Attributs du produit

    Anti-Dystrophin/DMD Antibody. Tested in Flow Cytometry, IHC, IHC-F, ICC, WB applications. This antibody reacts with Human, Mouse, Rat.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human Dystrophin recombinant protein (Position: H3076-D3404). Human Dystrophin shares 100% amino acid (aa) sequence identity with mouse Dystrophin.

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL, Human, Mouse, Rat Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL, Human, Mouse, Rat Immunohistochemistry (Frozen Section), 0.5-1 μg/mL, Human Immunocytochemistry, 0.5-1 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains antibody formulated with stabilizing components, 0.9 mg NaCl, 0.2 mg Na2HPO4, and 0.05 mg Sodium 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,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

    Date de péremption

    12 months
  • Antigène

    Dystrophin (DMD)

    Autre désignation

    DMD

    Sujet

    Background: Dystrophin, also known as DMD, is a rod-shaped cytoplasmic protein, and a vital part of a protein complex that connects the cytoskeleton of a muscle fiber to the surrounding extracellular matrix through the cell membrane. It is mapped to Xp21.2-p21.1. This complex is variously known as the costamere or thedystrophin-associated protein complex. Many muscle proteins, such as α-dystrobrevin, syncoilin, synemin, sarcoglycan, dystroglycan, and sarcospan, colocalize with dystrophin at the costamere. Dystrophin is a protein located between the sarcolemma and the outermost layer of myofilaments in the muscle fiber (myofiber). It is a cohesive protein, linking actin filaments to another support protein that resides on the inside surface of each muscle fiber's plasma membrane (sarcolemma).

    Gene Full Name: dystrophin

    Sequence Similarities: Contains 2 CH (calponin-homology) domains.

    Poids moléculaire

    427 kDa

    ID gène

    1756

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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