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CEP41 Protein (Myc-DYKDDDDK Tag)

CEP41 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2734444
  • Target See all CEP41 Proteins
    CEP41 (Centrosomal Protein 41kDa (CEP41))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 5
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This CEP41 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human TSGA14 / CEP41 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 CEP41 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
    CEP41 (Centrosomal Protein 41kDa (CEP41))
    Alternative Name
    Tsga14,cep41 (CEP41 Products)
    Synonyms
    1700017E11Rik Protein, 2810431D15Rik Protein, AI449046 Protein, AI503610 Protein, Tsga14 Protein, JBTS15 Protein, TSGA14 Protein, Cep41-A Protein, tsga14 Protein, RPL37A Protein, centrosomal protein 41 Protein, centrosomal protein 41kDa S homeolog Protein, Cep41 Protein, CEP41 Protein, cep41.S Protein
    Background
    This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15 an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    41.2 kDa
    NCBI Accession
    NP_061188
    Pathways
    M Phase
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