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Dystrophin antibody

The Rabbit Polyclonal anti-Dystrophin antibody has been validated for IHC, WB and IF. It is suitable to detect Dystrophin in samples from Human, Mouse and Rat.
Catalog No. ABIN7008615

Quick Overview for Dystrophin antibody (ABIN7008615)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

Reactivity

  • 107
  • 16
  • 14
  • 2
Human, Mouse, Rat

Host

  • 73
  • 36
Rabbit

Clonality

  • 83
  • 26
Polyclonal

Conjugate

  • 51
  • 7
  • 5
  • 5
  • 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
  • 16
  • 15
  • 13
  • 6
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Western Blotting (WB), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human DMD (NP_004007.1).

    Isotype

    IgG
  • Application Notes

    WB 1:200-1:2000 IHC 1:50-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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. Avoid freeze / thaw cycles.
  • Target

    Dystrophin (DMD)

    Alternative Name

    DMD

    Background

    This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene.

    Molecular Weight

    Observed_MW: 427 kDa

    Calculated_MW: 57-72 kDa/271 kDa/425-426 kDa

    Gene ID

    1756

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
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