Overview

  • Product nameAnti-ZNF468 antibody
    See all ZNF468 primary antibodies
  • Description
    Mouse polyclonal to ZNF468
  • Tested applicationsSuitable for: WB, ICC/IFmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    Full length Human ZNF468 protein (NP_954583.1).

  • Positive control
    • Human pancreas tissue lysate, ZNF468 transfected 293T cell line lysate and HepG2 cells.

Properties

Associated products

Applications

Our Abpromise guarantee covers the use of ab88862 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
WB Use a concentration of 1 µg/ml. Predicted molecular weight: 60 kDa.
ICC/IF Use a concentration of 10 µg/ml.

Target

  • RelevanceZNF468 belongs to the PtdIns transfer protein family, Class IIB subfamily. Its function is to mediate the monomeric transport of lipids by shielding a lipid from the aqueous environment and binding the lipid in a hydrophobic cavity. Ubiquitously expressed. There are two named isoforms.
  • Cellular localizationNuclear
  • Database links
  • Alternative names
    • Zinc finger protein 468 antibody

Anti-ZNF468 antibody images

  • Anti-ZNF468 antibody (ab88862) at 1 µg/ml + Human pancreas tissue lysate at 50 µg

    Predicted band size : 60 kDa
    Observed band size : 54 kDa (why is the actual band size different from the predicted?)
    Additional bands at : 49 kDa,70 kDa. We are unsure as to the identity of these extra bands.
  • All lanes : Anti-ZNF468 antibody (ab88862) at 1 µg/ml

    Lane 1 : ZNF468 transfected 293T cell line lysate
    Lane 2 : Non-transfected lysate

    Lysates/proteins at 25 µg per lane.


    Predicted band size : 60 kDa
    Observed band size : 48 kDa (why is the actual band size different from the predicted?)
  • ab88862, at 10 µg/ml staining ZNF468 in HepG2 cells by Immunofluorescence.

References for Anti-ZNF468 antibody (ab88862)

ab88862 has not yet been referenced specifically in any publications.

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