Overview

  • Product name

  • Description

    Rabbit polyclonal to RABGAP1
  • Host species

    Rabbit
  • Tested applications

    Suitable for: IPmore details
    Unsuitable for: WB
  • Species reactivity

    Reacts with: Human
    Predicted to work with: Mouse, Orangutan
  • Immunogen

    Synthetic peptide within Human RABGAP1 aa 25-75. The exact sequence is proprietary.
    Database link: Q9Y3P9

  • Positive control

    • IP: RABGAP1 IP in HeLa whole cell lysate.

Properties

Applications

Our Abpromise guarantee covers the use of ab241416 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
IP Use at 2-10 µg/mg of lysate.
  • Application notes
    Is unsuitable for WB.
  • Target

    • Relevance

      May act as a GTPase-activating protein of RAB6A. May play a role in microtubule nucleation by centrosome. May participate in a RAB6A-mediated pathway involved in the metaphase-anaphase transition.
    • Cellular localization

      Cytoplasm, cytosol. Centrosome
    • Database links

    • Alternative names

      • GAP and centrosome associated protein antibody
      • GAPCENA antibody
      • HSPC094 antibody
      • Rab GTPase activating protein 1 antibody
      • Rab6 GTPase activating protein GAPCenA antibody
      • RP11-123N4.2 antibody
      • TBC1 domain family member 11 antibody
      • TBC1D11 antibody
      see all

    Images

    • RABGAP1 was immunoprecipitated from HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate (1 mg for IP, 20% of IP loaded) with ab241416 at 6 µg/reaction. Western blot was performed from the immunoprecipitate using ab241416 at 1 µg/ml.

      Lane 1: ab241416 IP in HeLa whole cell lysate.
      Lane 2: Control IgG IP in HeLa whole cell lysate.

      Detection: Chemiluminescence with exposure time of 30 seconds.

      Lysates prepared in NETN buffer.

    References

    ab241416 has not yet been referenced specifically in any publications.

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