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Dystrophin antibody

The Mouse Monoclonal anti-Dystrophin antibody has been validated for IHC, WB and ELISA. It is suitable to detect Dystrophin in samples from Human.
Rockland
Catalog No. ABIN6657490
Supplier Product No.: 200-301-p36

Quick Overview for Dystrophin antibody (ABIN6657490)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

Reactivity

  • 107
  • 17
  • 15
  • 2
Human

Host

  • 72
  • 37
Mouse

Clonality

  • 82
  • 27
Monoclonal

Conjugate

  • 51
  • 7
  • 5
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  • 5
  • 5
  • 5
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This Dystrophin antibody is un-conjugated

Application

  • 82
  • 50
  • 31
  • 15
  • 15
  • 13
  • 6
  • 4
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  • 2
  • 1
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Immunohistochemistry (IHC), Western Blotting (WB), ELISA

Clone

MANDYS8
  • Supplier Product No.

    200-301-p36

    Supplier

    Rockland

    Purpose

    Dystrophin Antibody

    Cross-Reactivity (Details)

    This product reacts with human, mouse, rat, and rabbit.

    Purification

    Anti-Dystrophin antibody was purified from mouse ascites by protein A chromatography.

    Immunogen

    Dystrophin antibody was produced in mice by repeated immunizations with recombinant protein corresponding to human dystrophin fragment.

    Isotype

    IgG2b
  • Application Notes

    ELISA_Dilution: 1:20,000

    Immunohistochemistry_Dilution: 1:100-1:500

    Western_Blot_Dilution: 1-2 μg/mL

    Comment

    Anti-Dystrophin is tested for Immunohistochemistry -F and Western Blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately ~425 kDa corresponding to the appropriate cell lysate or extract.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Reconstitution_Buffer: Neutral PBS

    Reconstitution_Volume: 200μL

    Buffer

    Buffer: 1.2 % sodium acetate

    Stabilizer: 2 mg BSA

    Preservative: 0.01 % (w/v) Sodium 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,-20 °C

    Storage Comment

    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Expiry Date

    12 months
  • Target

    Dystrophin (DMD)

    Alternative Name

    Dystrophin

    Background

    Synonyms: BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272

    Background: Dystrophin(DMD) gene has 79 exons spanning at least 2,300 kb (2.3 Mb). The C terminus of the dystrophin protein is encoded by a highly conserved, alternatively spliced region of the gene. beta-dystroglycan binding activity is expressed by the dystrophin fragment spanning amino acids 3026-3345 containing the ZZ domain. DMD transcript is formed by at least 60 exons, the first half of the transcript is formed by a minimum of 33 exons spanning nearly 1000 kb, and the remaining portion has at least 27 exons that may spread over a similar distance. Dystrophin gene is expressed at a higher level in primary cultures of neuronal cells than in astro-glial cells derived from adult mouse brain. overexpression of dystrophin prevents the development of the abnormal mechanical properties associated with dystrophic muscle without causing deleterious side effects. This antibody is suitable for researchers interested in Muscular Dystrophies and Dystrophin-Glycoprotein Complexes and cardiovascular research.

    Gene Name: DMD

    Gene ID

    1756

    NCBI Accession

    NP_000100

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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