Anti-TCP1 Antibody (Clone#2E7)

筛选器： All WB IHC ICC/IF FCM

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  Western blot analysis of anti-TCP1 antibody (M02389). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human MCF-7 whole cell lysates,
  Lane 3: human COLO-320 whole cell lysates,
  Lane 4: human HepG2 whole cell lysates,
  Lane 5: human A431 whole cell lysates,
  Lane 6: human HT1080 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-TCP1 antigen affinity purified monoclonal antibody (M02389) 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 TCP1 at approximately 60 kDa. The expected band size for TCP1 is at 60 kDa.

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  IHC analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with mouse anti-TCP1 Antibody (M02389) at a dilution of 1:200 and developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.

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  IHC analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with mouse anti-TCP1 Antibody (M02389) at a dilution of 1:200 and developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.

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  IF analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in an immunocytochemical section of MCF-7 cells. 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 HepG2 cells using anti-TCP1 antibody (M02389).
  Overlay histogram showing HepG2 cells stained with A04887-1 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with mouse anti-TCP1 Antibody ((M02389, 1:100). DyLight®488 conjugated goat anti-mouse IgG (BA1126, 1:100) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG (Catalog # BA1046) (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.

• 

  Western blot analysis of anti-TCP1 antibody (M02389). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Hela whole cell lysates,
  Lane 2: human MCF-7 whole cell lysates,
  Lane 3: human COLO-320 whole cell lysates,
  Lane 4: human HepG2 whole cell lysates,
  Lane 5: human A431 whole cell lysates,
  Lane 6: human HT1080 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-TCP1 antigen affinity purified monoclonal antibody (M02389) 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 TCP1 at approximately 60 kDa. The expected band size for TCP1 is at 60 kDa.

• 

  IHC analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with mouse anti-TCP1 Antibody (M02389) at a dilution of 1:200 and developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.

• 

  IHC analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with mouse anti-TCP1 Antibody (M02389) at a dilution of 1:200 and developed using HRP Conjugated mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.

• 

  IF analysis of TCP1 using anti-TCP1 antibody (M02389).
  TCP1 was detected in an immunocytochemical section of MCF-7 cells. 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 HepG2 cells using anti-TCP1 antibody (M02389).
  Overlay histogram showing HepG2 cells stained with A04887-1 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with mouse anti-TCP1 Antibody ((M02389, 1:100). DyLight®488 conjugated goat anti-mouse IgG (BA1126, 1:100) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG (Catalog # BA1046) (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.