Anti-TRIM33 Antibody (Clone#8I8)

筛选器： All WB IHC ICC/IF FCM

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  Western blot analysis of TRIM33 using anti-TRIM33 antibody (M03133-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human MCF-7 whole cell lysates,
  Lane 2: human SW620 whole cell lysates,
  Lane 3: human K562 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-TRIM33 antigen affinity purified monoclonal antibody (M03133-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TRIM33 at approximately 150 kDa. The expected band size for TRIM33 is at 123 kDa.

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  IHC analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.

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  IHC analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.

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  IF analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in an immunocytochemical section of Hela cells. The section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

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  Flow Cytometry analysis of HL-60 cells using anti-TRIM33 antibody (M03133-2).
  Overlay histogram showing HL-60 cells stained with M03133-2 (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 mouse anti-TRIM33 Antibody (M03133-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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.

• 

  Western blot analysis of TRIM33 using anti-TRIM33 antibody (M03133-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human MCF-7 whole cell lysates,
  Lane 2: human SW620 whole cell lysates,
  Lane 3: human K562 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-TRIM33 antigen affinity purified monoclonal antibody (M03133-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TRIM33 at approximately 150 kDa. The expected band size for TRIM33 is at 123 kDa.

• 

  IHC analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.

• 

  IHC analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.

• 

  IF analysis of TRIM33 using anti-TRIM33 antibody (M03133-2).
  TRIM33 was detected in an immunocytochemical section of Hela cells. The section was incubated with mouse anti-TRIM33 Antibody (M03133-2) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

• 

  Flow Cytometry analysis of HL-60 cells using anti-TRIM33 antibody (M03133-2).
  Overlay histogram showing HL-60 cells stained with M03133-2 (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 mouse anti-TRIM33 Antibody (M03133-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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.