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FNBP4 Protein (Myc-DYKDDDDK Tag)

FNBP4 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2721311
  • Target See all FNBP4 products
    FNBP4 (Formin Binding Protein 4 (FNBP4))
    Protein Type
    Recombinant
    Origin
    • 1
    • 1
    Human
    Source
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This FNBP4 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Formin-binding protein 4 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 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
    FNBP4 (Formin Binding Protein 4 (FNBP4))
    Alternative Name
    Formin-Binding Protein 4 (FNBP4 Products)
    Synonyms
    MGC105867 Protein, MGC69033 Protein, FBP30 Protein, Fnbp30 Protein, mKIAA1014 Protein, formin binding protein 4 Protein, formin binding protein 4 L homeolog Protein, formin-binding protein 4 Protein, Fnbp4 Protein, fnbp4.L Protein, fnbp4 Protein, FNBP4 Protein, LOC734003 Protein
    Background
    This gene encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome.
    Molecular Weight
    110.1 kDa
    NCBI Accession
    NP_056123
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