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HPS4 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

HPS4 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2723038
  • Target See all HPS4 Proteins
    HPS4 (Hermansky-Pudlak Syndrome 4 (HPS4))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 2
    • 2
    Human
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This HPS4 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human HPS4 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product HPS4 Protein
  • 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
    HPS4 (Hermansky-Pudlak Syndrome 4 (HPS4))
    Alternative Name
    Hps4 (HPS4 Products)
    Synonyms
    LE Protein, 2010205O06Rik Protein, AU040608 Protein, BLOC-3 Protein, C130020P05Rik Protein, le Protein, mKIAA1667 Protein, HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 Protein, HPS4 Protein, Hps4 Protein
    Background
    This gene encodes a protein component of biogenesis of lysosome-related organelles complexes (BLOC). BLOC complexes are important for the formation of endosomal-lysosomal organelles such as melanosomes and platelet dense granules. Mutations in this gene result in subtype 4 of Hermansky-Pudlak syndrome, a form of albinism. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    76.7 kDa
    NCBI Accession
    NP_071364
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