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Dystrophin antibody

The Rabbit Polyclonal anti-Dystrophin antibody is suitable to detect Dystrophin in samples from Human, Mouse and Rat. It has been validated for IHC and IF.
Catalog No. ABIN8121096
$225.50
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Dystrophin antibody (ABIN8121096)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

Reactivity

  • 125
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  • 3
  • 2
Human, Mouse, Rat

Host

  • 75
  • 51
Rabbit

Clonality

  • 90
  • 36
Polyclonal

Conjugate

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

Application

  • 67
  • 41
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  • 2
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Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    DMD Antibody

    Specificity

    DMD Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from part region of human protein

    Isotype

    IgG
  • Application Notes

    IHC 1:50-300. IF 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % 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

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    Dystrophin (DMD)

    Alternative Name

    DMD

    Background

    Background: dystrophin(DMD) Homo sapiens The dystrophin gene is the largest gene found in nature, measuring 2.4 Mb. The gene was identified through a positional cloning approach, targeted at the isolation of the gene responsible for Duchenne (DMD) and Becker (BMD) Muscular Dystrophies. DMD is a recessive, fatal, X-linked disorder occurring at a frequency of about 1 in 3,500 new-born males. BMD is a milder allelic form. In general, DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations), while in BMD patients dystrophin is reduced either in molecular weight (derived from in-frame deletions) or in expression level. The dystrophin gene is highly complex, containing at least eight independent, tissue-specific promoters and two polyA-addition sites. Furthermore, dystrophin RNA is differentially spliced, producing a range of different transcripts, encoding a large set of protein isoforms. Dystrophin (as enc

    Gene Name: DMD

    Protein Name: Dystrophin

    Gene ID

    1756

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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