Anti-ATF6 Antibody

筛选器： All WB ICC/IF FCM ELISA

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  Western blot analysis of anti- ATF6 antibody (A00655-4). The sample well of each lane was loaded with 30ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human 293T whole cell lysates,
  Lane 3: human K562 whole cell lysates,
  Lane 4: human MCF-7 whole cell lysates.
  Use rabbit anti- ATF6 1:1000, probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog#EK1002). A specific band was detected for ATF6 at approximately 90-100KD. The expected band size for ATF6 is at 75KD.

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  IF analysis of ATF6 using anti-ATF6 antibody (A00655-4).
  ATF6 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with rabbit anti-ATF6 Antibody (A00655-4) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

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  Flow Cytometry analysis of SiHa cells using anti-ATF6 antibody (A00655-4).
  Overlay histogram showing SiHa cells stained with A00655-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATF6 Antibody (A00655-4) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Western blot analysis of anti- ATF6 antibody (A00655-4). The sample well of each lane was loaded with 30ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human 293T whole cell lysates,
  Lane 3: human K562 whole cell lysates,
  Lane 4: human MCF-7 whole cell lysates.
  Use rabbit anti- ATF6 1:1000, probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog#EK1002). A specific band was detected for ATF6 at approximately 90-100KD. The expected band size for ATF6 is at 75KD.

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  IF analysis of ATF6 using anti-ATF6 antibody (A00655-4).
  ATF6 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with rabbit anti-ATF6 Antibody (A00655-4) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

• 

  Flow Cytometry analysis of SiHa cells using anti-ATF6 antibody (A00655-4).
  Overlay histogram showing SiHa cells stained with A00655-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATF6 Antibody (A00655-4) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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