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Dysferlin Protein (DYSF) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

This Recombinant Dysferlin protein is produced in HEK-293 Cells.
Catalog No. ABIN2719887

Quick Overview for Dysferlin Protein (DYSF) (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2719887)

Target

Dysferlin (DYSF)

Protein Type

Recombinant

Origin

Human

Source

  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This Dysferlin protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human Dysferlin (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    Dysferlin (DYSF)

    Alternative Name

    Dysferlin

    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.

    Molecular Weight

    241.2 kDa

    NCBI Accession

    NP_001124459
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