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BBS4 Protein (Bardet-Biedl Syndrome 4) (Myc-DYKDDDDK Tag)

BBS4 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2715167
$1,019.70
Zzgl. Versandkosten $45.00 und $20.00 Trockeneis
20 μg
Lieferung in 11 Werktagen
  • Target Alle BBS4 Proteine anzeigen
    BBS4 (Bardet-Biedl Syndrome 4 (BBS4))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 1
    Human
    Quelle
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses BBS4 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human BBS4 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 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
    BBS4 (Bardet-Biedl Syndrome 4 (BBS4))
    Andere Bezeichnung
    Bbs4 (BBS4 Produkte)
    Synonyme
    CG13232, Dmel\\CG13232, zgc:152964, AW537059, AW742241, D9Ertd464e, Bardet-Biedl syndrome 4, bardet-biedl syndrome 4, Bardet-Biedl syndrome 4 (human), BBS4, bbs4, Bbs4
    Hintergrund
    This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein&aposs shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants.
    Molekulargewicht
    58.1 kDa
    NCBI Accession
    NP_149017
    Pathways
    Hedgehog Signalweg, Tube Formation, Maintenance of Protein Location
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