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WDR73 Protein (Myc-DYKDDDDK Tag)

WDR73 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2735532
  • Target Alle WDR73 Proteine anzeigen
    WDR73 (WD Repeat Domain 73 (WDR73))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 1
    • 1
    Human
    Quelle
    • 2
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses WDR73 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human WDR73 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 WDR73 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
    WDR73 (WD Repeat Domain 73 (WDR73))
    Andere Bezeichnung
    Wdr73 (WDR73 Produkte)
    Synonyme
    1200011I23Rik Protein, 2410008B13Rik Protein, AI848574 Protein, C85352 Protein, zgc:112071 Protein, WD repeat domain 73 Protein, WD repeat domain 73 L homeolog Protein, WDR73 Protein, Wdr73 Protein, wdr73.L Protein, wdr73 Protein
    Hintergrund
    The protein encoded by this gene is thought to contain multiple WD40 repeats. WD40 repeats are motifs that contain 40-60 amino acids, and usually end with Trp-Asp (WD). This protein is found in the cytoplasm during interphase, but accumulates at the spindle poles and astral microtubules during mitosis. Reduced expression of this gene results in abnormalities in the size and morphology of the nucleus. Mutations in this gene have been associated with Galloway-Mowat syndrome PMID: 25466283), which is a rare autosomal recessive disorder that affects both the central nervous system and kidneys. Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    41.5 kDa
    NCBI Accession
    NP_116245
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