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Recombinant Dystrophin antibody (AA 1700-2300)

The Rabbit Monoclonal anti-Dystrophin antibody is suitable to detect Dystrophin in samples from Human. It has been validated for IHC, WB and IF.
Catalog No. ABIN7864334
$640.46
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Quick Overview for Recombinant Dystrophin antibody (AA 1700-2300) (ABIN7864334)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

Antibody Type

Recombinant Antibody

Reactivity

  • 112
  • 18
  • 17
  • 3
  • 2
Human

Host

  • 75
  • 38
Rabbit

Clonality

  • 88
  • 25
Monoclonal

Conjugate

  • 68
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This Dystrophin antibody is un-conjugated

Application

  • 56
  • 31
  • 30
  • 28
  • 26
  • 11
  • 10
  • 8
  • 4
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), Western Blotting (WB), Immunofluorescence (IF)

Clone

DMD-8773R
  • Binding Specificity

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

    Purpose

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

    Specificity

    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.

    Immunogen

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

    Isotype

    IgG, kappa
  • Application Notes

    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.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C

    Storage Comment

    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.
  • Target

    Dystrophin (DMD)

    Alternative Name

    Dystrophin

    Background

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

    Human skeletal muscle and heart muscle tissues (IHC).

    Molecular Weight

    427kDa

    Gene ID

    1756, 495912

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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