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TSEN34 Protein (His tag)

TSEN34 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2734440
  • Target See all TSEN34 Proteins
    TSEN34 (tRNA Splicing Endonuclease 34 Homolog (TSEN34))
    Protein Type
    Recombinant
    Origin
    • 3
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This TSEN34 protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human TSEN34 / SEN34 (N-term HIS tag, transcript variant 1) 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 TSEN34 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
    TSEN34 (tRNA Splicing Endonuclease 34 Homolog (TSEN34))
    Alternative Name
    Tsen34,sen34 (TSEN34 Products)
    Synonyms
    LENG5 Protein, SEN34 Protein, 0610027F08Rik Protein, Leng5 Protein, PCH2C Protein, SEN34L Protein, tRNA splicing endonuclease subunit 34 Protein, tRNA splicing endonuclease 34 homolog (S. cerevisiae) Protein, Tsen34 Protein, TSEN34 Protein, tsen34 Protein
    Background
    This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]
    Molecular Weight
    33.5 kDa
    NCBI Accession
    NP_076980
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