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Dysferlin antibody

This Rabbit Monoclonal antibody specifically detects Dysferlin in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7266868

Quick Overview for Dysferlin antibody (ABIN7266868)

Target

See all Dysferlin (DYSF) Antibodies
Dysferlin (DYSF)

Reactivity

  • 60
  • 25
  • 5
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
Human

Host

  • 54
  • 5
  • 1
Rabbit

Clonality

  • 47
  • 13
Monoclonal

Conjugate

  • 27
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Dysferlin antibody is un-conjugated

Application

  • 20
  • 17
  • 15
  • 15
  • 9
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Purpose

    Dysferlin (Romeo) Rabbit mAb

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Dysferlin (Romeo)

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    Dysferlin (DYSF)

    Alternative Name

    DYSF

    Background

    The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008],FER1L1, LGMD2B, MMD1,Cell Biology & Developmental Biology,DYSF

    Molecular Weight

    280kDa

    Gene ID

    8291

    UniProt

    O75923
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