Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-200 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-200 |
Flow Cytometry (FCM): | 1:50 |
Western blot analysis of anti-TOM20/TOMM20 antibody (BM4366). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human K562 whole cell lysates,
Lane 4: human Hela whole cell lysates,
Lane 5: rat kidney tissue lysates,
Lane 6: rat stomach tissue lysates,
Lane 7: mouse kidney tissue lysates,
Lane 8: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TOM20/TOMM20 antigen affinity purified monoclonal antibody (BM4366) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TOM20/TOMM20 at approximately 16 kDa. The expected band size for TOM20/TOMM20 is at 16 kDa.
IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (BM4366) .
TOM22/TOMM22 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. The tissue section was incubated with rabbit anti-TOM22/TOMM22 Antibody (BM4366) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (BM4366) .
TOM22/TOMM22 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-TOM22/TOMM22 Antibody (BM4366) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Immunofluorescent analysis of Hela cells, using TOMM20 Antibody.
Western blot analysis of anti-TOM20/TOMM20 antibody (BM4366). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human K562 whole cell lysates,
Lane 4: human Hela whole cell lysates,
Lane 5: rat kidney tissue lysates,
Lane 6: rat stomach tissue lysates,
Lane 7: mouse kidney tissue lysates,
Lane 8: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TOM20/TOMM20 antigen affinity purified monoclonal antibody (BM4366) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TOM20/TOMM20 at approximately 16 kDa. The expected band size for TOM20/TOMM20 is at 16 kDa.
IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (BM4366) .
TOM22/TOMM22 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. The tissue section was incubated with rabbit anti-TOM22/TOMM22 Antibody (BM4366) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (BM4366) .
TOM22/TOMM22 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-TOM22/TOMM22 Antibody (BM4366) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Immunofluorescent analysis of Hela cells, using TOMM20 Antibody.