Western blot (WB): | 1:2000 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:100 |
Flow cytometry (FCM): | 1:100 |
Western blot analysis of anti-SMAD2 antibody (M00090-4). 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 HEL whole cell lysates,
Lane 3: human RT4 whole cell lysates,
Lane 4: human A549 whole cell lysates,
Lane 5: mouse skeletal muscle lysates,
Lane 6: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-SMAD2 antigen affinity purified monoclonal antibody (M00090-4) 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 SMAD2 at approximately 52 kDa. The expected band size for SMAD2 is at 52 kDa.
Flow cytometric analysis of living 293T cells transfected with SMAD2 overexpression plasmid , Red)/empty vector (Blue) using anti-SMAD2 antibody. Cells incubated with a non-specific antibody (Green) were used as isotype control (1:100).
Flow cytometric Analysis of permeabilized HUVEC cells, using anti-SMAD2 antibody, (Red), compared to an IgG isotype control, (green) (1:100).
Flow cytometric Analysis of Jurkat cells, using anti-SMAD2 antibody, (Red), compared to a nonspecific negative control antibody, (Blue).
Immunofluorescent staining of 293T cells transfected by pCMV6-ENTRY SMAD2 using anti-SMAD2 antibody. 293T cells transfected with empty vector served as a negative control (right) (1:100).
Western blot analysis of anti-SMAD2 antibody (M00090-4). 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 HEL whole cell lysates,
Lane 3: human RT4 whole cell lysates,
Lane 4: human A549 whole cell lysates,
Lane 5: mouse skeletal muscle lysates,
Lane 6: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-SMAD2 antigen affinity purified monoclonal antibody (M00090-4) 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 SMAD2 at approximately 52 kDa. The expected band size for SMAD2 is at 52 kDa.
Flow cytometric analysis of living 293T cells transfected with SMAD2 overexpression plasmid , Red)/empty vector (Blue) using anti-SMAD2 antibody. Cells incubated with a non-specific antibody (Green) were used as isotype control (1:100).
Flow cytometric Analysis of permeabilized HUVEC cells, using anti-SMAD2 antibody, (Red), compared to an IgG isotype control, (green) (1:100).
Flow cytometric Analysis of Jurkat cells, using anti-SMAD2 antibody, (Red), compared to a nonspecific negative control antibody, (Blue).
Immunofluorescent staining of 293T cells transfected by pCMV6-ENTRY SMAD2 using anti-SMAD2 antibody. 293T cells transfected with empty vector served as a negative control (right) (1:100).