Aurora-C Antibody

CAT:
800-F50011-0.08ML
Size:
0.08 mL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Aurora-C Antibody - image 1

Aurora-C Antibody

  • Description:

    Chromosomal segregation during mitosis as well as meiosis is regulated by kinases and phosphatases. The Aurora kinases, members of the Ser/Thr protein kinase family, associate with microtubules during chromosome movement and segregation. Aurora kinase C may play a part in organizing microtubules in relation to the function of the centrosome/spindle pole during mitosis. This protein is localized to centrosome from anaphase to cytokinesis. Expression is limited to testis in normal cells. Elevated expression levels are seen only in a subset of cancer cells such as HepG2, HuH7 and HeLa cells. Aurora-C expression is maximum at M phase.
  • Specifications:

    Western blot: 1:1000
  • UniProt:

    Q9UQB9
  • Host:

    Rabbit
  • Reactivity:

    Human
  • Immunogen:

    A portion of amino acids 3-38 from the human protein was used as the immunogen for this Aurora-C antibody.
  • Clonality:

    Polyclonal
  • Isotype:

    Ig
  • Applications:

    WB, ELISA
  • Purity:

    Antigen affinity
  • Format:

    Antigen affinity purified
  • Buffer:

    In 1X PBS, pH 7.4, with 0.09% sodium azide
  • Reconstitution:

    Aliquot the Aurora-C antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Limitations:

    This Aurora-C antibody is available for research use only.
  • Storage Conditions:

    Aliquot the Aurora-C antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Formulation:

    In 1X PBS, pH 7.4, with 0.09% sodium azide
  • Applications Notes:

    Titration of the Aurora-C antibody may be required due to differences in protocols and secondary/substrate sensitivity.
  • CAS Number:

    9007-83-4
  • Image Legend:

    Immunofluorescence staining of HeLa cells expressing GFP-Aurora-C performed at different cellular mitotic stages with the A) Aurora-C antibody, B) GFP fluorescence, C) DAPI nuclear staining, and D) anti-Aurora C merged to DAPI staining.