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VPS13B Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag)

VPS13B Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2735414
  • Target See all VPS13B products
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 4
    Origin
    Human
    Source
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This VPS13B protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human VPS13B (transcript variant 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
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Alternative Name
    Vps13b (VPS13B Products)
    Synonyms
    1810042B05Rik Protein, 2310042E16Rik Protein, 4732488H20 Protein, C330002D13Rik Protein, C87206 Protein, Coh1 Protein, D230005K13 Protein, mKIAA0532 Protein, mKIAA5032 Protein, CHS1 Protein, COH1 Protein, Cohh1 Protein, vacuolar protein sorting 13 homolog B Protein, vacuolar protein sorting 13B Protein, VPS13B Protein, Vps13b Protein
    Background
    This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene.
    Molecular Weight
    47 kDa
    NCBI Accession
    NP_858047
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