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DTNA Protein (Transcript Variant 5) (Myc-DYKDDDDK Tag)

This Recombinant DTNA protein is expressed in HEK-293 Cells.
Catalog No. ABIN2719789
$1,112.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Will be delivered in 11 Business Days

Quick Overview for DTNA Protein (Transcript Variant 5) (Myc-DYKDDDDK Tag) (ABIN2719789)

Target

See all DTNA Proteins
DTNA (Dystrobrevin alpha (DTNA))

Protein Type

Recombinant

Origin

  • 6
  • 2
Human

Source

  • 4
  • 2
  • 1
  • 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 5

    Purification tag / Conjugate

    This DTNA protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human DTNA / DRP3 (transcript variant 5) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
    Expression System
    Conjugate
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    Expression System HEK-293 Cells
    Conjugate His tag
    Origin Human
    Price starts at $13,686.36
    Expression System Cell-free protein synthesis (CFPS)
    Conjugate Strep Tag
    Origin Human
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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

    DTNA (Dystrobrevin alpha (DTNA))

    Alternative Name

    Dtna,drp3

    Background

    The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.

    Molecular Weight

    58.7 kDa

    NCBI Accession

    NP_116761
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