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GTPBP3 Protein (Transcript Variant V) (Myc-DYKDDDDK Tag)

GTPBP3 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2722360
  • Target See all GTPBP3 Proteins
    GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant V
    Origin
    • 3
    • 1
    • 1
    Human
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This GTPBP3 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human GTPBP3 / MTGP1 (transcript variant V) 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 GTPBP3 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
    GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))
    Alternative Name
    Gtpbp3,mtgp1 (GTPBP3 Products)
    Synonyms
    GTPBP3 Protein, zgc:112394 Protein, 2410009F13Rik Protein, AI607903 Protein, GTPBG3 Protein, MSS1 Protein, MTGP1 Protein, THDF1 Protein, GTP binding protein 3, mitochondrial Protein, GTP binding protein 3 Protein, GTPBP3 Protein, Gtpbp3 Protein, gtpbp3 Protein
    Background
    This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described.
    Molecular Weight
    51.9 kDa
    NCBI Accession
    NP_116009
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