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BCAP31 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

This Recombinant BCAP31 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2715172
$956.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
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Quick Overview for BCAP31 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag) (ABIN2715172)

Target

See all BCAP31 Proteins
BCAP31 (B-Cell Receptor-Associated Protein 31 (BCAP31))

Protein Type

Recombinant

Origin

Human

Source

  • 2
  • 2
  • 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 2

    Purification tag / Conjugate

    This BCAP31 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human BCAP31 / BAP31 (transcript variant 2) 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

    BCAP31 (B-Cell Receptor-Associated Protein 31 (BCAP31))

    Alternative Name

    Bcap31,bap31

    Background

    This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16.

    Molecular Weight

    27.8 kDa

    NCBI Accession

    NP_005736

    Pathways

    Positive Regulation of Endopeptidase Activity
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