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KLC2 Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag)

KLC2 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2724276
  • Target Alle KLC2 Proteine anzeigen
    KLC2 (Kinesin Light Chain 2 (KLC2))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 4
    Spezies
    • 4
    • 1
    Human
    Quelle
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses KLC2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human KLC2 (transcript variant 4) 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 KLC2 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
    KLC2 (Kinesin Light Chain 2 (KLC2))
    Andere Bezeichnung
    Klc2 (KLC2 Produkte)
    Synonyme
    MGC143149 Protein, wu:fc15b01 Protein, wu:fj62c06 Protein, zgc:162288 Protein, DKFZp459K0951 Protein, 8030455F02Rik Protein, AW212649 Protein, KLC 2 Protein, KLC-2 Protein, kinesin light chain 2 Protein, KLC2 Protein, klc2 Protein, Klc2 Protein
    Hintergrund
    The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome.
    Molekulargewicht
    68.8 kDa
    NCBI Accession
    NP_001128248
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