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NDE1 Protein (NDE1) (Transcript Variant 2) (Myc-DYKDDDDK Tag)

NDE1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2726912
  • Target Alle NDE1 Proteine anzeigen
    NDE1
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 2
    Spezies
    • 4
    • 1
    Human
    Quelle
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses NDE1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human NDE1 (transcript variant 2) 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 NDE1 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
    NDE1
    Andere Bezeichnung
    Nde1 (NDE1 Produkte)
    Synonyme
    2810027M15Rik Protein, AU042936 Protein, AW822251 Protein, Nude Protein, mNudE Protein, HOM-TES-87 Protein, LIS4 Protein, NDE Protein, NUDE Protein, NUDE1 Protein, fb82g01 Protein, im:7141877 Protein, wu:fb82g01 Protein, zgc:114109 Protein, nudE neurodevelopment protein 1 Protein, Nde1 Protein, NDE1 Protein, nde1 Protein
    Hintergrund
    This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    37.5 kDa
    NCBI Accession
    NP_060138
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