Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Dystrophin antibody

This Rabbit Monoclonal antibody specifically detects Dystrophin in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7880663
$625.62
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Dystrophin antibody (ABIN7880663)

Target

See all Dystrophin (DMD) Antibodies
Dystrophin (DMD)

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

  • 57
  • 31
  • 30
  • 28
  • 26
  • 12
  • 10
  • 8
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

AOGG-4
  • Purpose

    Dystrophin Antibody / DMD

    Purification

    Affinity purified

    Immunogen

    A synthetic peptide specific to human Dystrophin / DMD was used as the immunogen for the Dystrophin antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Dystrophin antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

    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 the Dystrophin antibody at -20oC.
  • Target

    Dystrophin (DMD)

    Alternative Name

    Dystrophin

    Background

    The DMD 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. [RefSeq]

    UniProt

    P11532

    Pathways

    Skeletal Muscle Fiber Development
You are here:
Chat with us!