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Pallidin Protein (Myc-DYKDDDDK Tag)

PLDN Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2728189
  • Target See all Pallidin (PLDN) Proteins
    Pallidin (PLDN) (Pallidin Homolog (PLDN))
    Protein Type
    Recombinant
    Origin
    • 5
    • 1
    Human
    Source
    • 2
    • 2
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This Pallidin protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Pallidin (PLDN) 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 PLDN 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
    Pallidin (PLDN) (Pallidin Homolog (PLDN))
    Alternative Name
    Pallidin (Pldn) (PLDN Products)
    Synonyms
    CG14133 Protein, Dmel\\CG14133 Protein, LOC100226487 Protein, pldn Protein, BLOS6 Protein, HPS9 Protein, PA Protein, PALLID Protein, PLDN Protein, Pldn Protein, BLOC-1 Protein, Stx13bp1 Protein, pa Protein, pallidin Protein, CG14133 gene product from transcript CG14133-RB Protein, biogenesis of lysosomal organelles complex 1 subunit 6 Protein, pallidin homolog (mouse) Protein, biogenesis of lysosomal organelles complex-1, subunit 6, pallidin Protein, Pallidin Protein, BLOC1S6 Protein, pldn Protein, Bloc1s6 Protein
    Background
    The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome.
    Molecular Weight
    19.6 kDa
    NCBI Accession
    NP_036520
    Pathways
    Synaptic Vesicle Exocytosis
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