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PQBP1 Protein (Transcript Variant 10) (Myc-DYKDDDDK Tag)

PQBP1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2729535
  • Target Alle PQBP1 Proteine anzeigen
    PQBP1 (Polyglutamine Binding Protein 1 (PQBP1))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 10
    Spezies
    • 10
    • 1
    • 1
    • 1
    Human
    Quelle
    • 5
    • 3
    • 2
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses PQBP1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human PQBP1 (transcript variant 10) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product PQBP1 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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
    PQBP1 (Polyglutamine Binding Protein 1 (PQBP1))
    Andere Bezeichnung
    Pqbp1 (PQBP1 Produkte)
    Synonyme
    PQBP1 Protein, MRX55 Protein, MRXS3 Protein, MRXS8 Protein, NPW38 Protein, RENS1 Protein, SHS Protein, PQBP-1 Protein, Sfc2 Protein, npw38 Protein, polyglutamine binding protein 1 Protein, PQBP1 Protein, Pqbp1 Protein
    Hintergrund
    This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked mental retardation. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009].
    Molekulargewicht
    19.2
    NCBI Accession
    NP_001161464
    Pathways
    Ribonucleoprotein Complex Subunit Organization
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