| Western blot (WB): | 1:1000-5000 |
| Immunohistochemistry (IHC): | 1:50-200 |
| Immunofluorescence (IF): | 1:50-200 |
| Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-200 |
| Flow Cytometry (FCM): | 1:30 |

Western blot analysis of anti-a-SMA/ACTA2 antibody (BM4172). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human A549 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-a-SMA/ACTA2 antigen affinity purified monoclonal antibody (BM4172) 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 a-SMA/ACTA2 at approximately 42 kDa. The expected band size for a-SMA/ACTA2 is at 42 kDa.

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using alpha smooth muscle Actin Antibody.

IF analysis of a-SMA/ACTA2 using anti-a-SMA/ACTA2 antibody (BM4172).
a-SMA/ACTA2 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-a-SMA/ACTA2 Antibody (BM4172) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

IF analysis of a-SMA/ACTA2 using anti-a-SMA/ACTA2 antibody (BM4172).
a-SMA/ACTA2 was detected in a paraffin-embedded section of rat brain vessel tissue. The tissue section was incubated with rabbit anti-a-SMA/ACTA2 Antibody (BM4172) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

Immunofluorescent analysis of A431 cells, using alpha smooth muscle Actin Antibody.

Western blot analysis of anti-a-SMA/ACTA2 antibody (BM4172). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human A549 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-a-SMA/ACTA2 antigen affinity purified monoclonal antibody (BM4172) 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 a-SMA/ACTA2 at approximately 42 kDa. The expected band size for a-SMA/ACTA2 is at 42 kDa.

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using alpha smooth muscle Actin Antibody.

IF analysis of a-SMA/ACTA2 using anti-a-SMA/ACTA2 antibody (BM4172).
a-SMA/ACTA2 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-a-SMA/ACTA2 Antibody (BM4172) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

IF analysis of a-SMA/ACTA2 using anti-a-SMA/ACTA2 antibody (BM4172).
a-SMA/ACTA2 was detected in a paraffin-embedded section of rat brain vessel tissue. The tissue section was incubated with rabbit anti-a-SMA/ACTA2 Antibody (BM4172) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

Immunofluorescent analysis of A431 cells, using alpha smooth muscle Actin Antibody.






