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KLC2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

KLC2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2724274
  • Target See all KLC2 Proteins
    KLC2 (Kinesin Light Chain 2 (KLC2))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 4
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This KLC2 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human KLC2 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product KLC2 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Storage
    -80 °C
    Storage Comment
    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))
    Alternative Name
    Klc2 (KLC2 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    68.8 kDa
    NCBI Accession
    NP_073733
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