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PABPC5 Protein (His tag)

PABPC5 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2728103
  • Target See all PABPC5 Proteins
    PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))
    Protein Type
    Recombinant
    Origin
    • 3
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This PABPC5 protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human PABPC5 (full length, N-term HIS tag) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product PABPC5 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 N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    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
    PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))
    Alternative Name
    Pabpc5 (PABPC5 Products)
    Synonyms
    PABPC5 Protein, PABP5 Protein, C820015E17 Protein, poly(A) binding protein cytoplasmic 5 Protein, poly A binding protein, cytoplasmic 5 Protein, poly(A) binding protein, cytoplasmic 5 Protein, PABPC5 Protein, Pabpc5 Protein
    Background
    This gene encodes a protein that binds to the polyA tail found at the 3' end of most eukaryotic mRNAs. It is thought to play a role in the regulation of mRNA metabolic processes in the cytoplasm. This gene is located in a gene-poor region within the X-specific 13d-sY43 subinterval of the chromosome Xq21.3/Yp11.2 homology block. It is located close to translocation breakpoints associated with premature ovarian failure, and is therefore a potential candidate gene for this disorder.
    Molecular Weight
    43.2 kDa
    NCBI Accession
    NP_543022
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