Western blot analysis of anti-α-SMA antibody (BM0002). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: rat stomach tissue lysates,
Lane 3: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-α-SMA antigen affinity purified polyclonal antibody (BM0002) 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 α-SMA at approximately 42 kDa. The expected band size for α-SMA is at 42 kDa.
IHC analysis of α-SMA using anti-α-SMA antibody (BM0002).
α-SMA was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of anti-α-SMA antibody (BM0002). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: rat stomach tissue lysates,
Lane 3: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-α-SMA antigen affinity purified polyclonal antibody (BM0002) 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 α-SMA at approximately 42 kDa. The expected band size for α-SMA is at 42 kDa.
IHC analysis of α-SMA using anti-α-SMA antibody (BM0002).
α-SMA was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of anti-α-SMA antibody (BM0002). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: rat stomach tissue lysates,
Lane 3: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-α-SMA antigen affinity purified polyclonal antibody (BM0002) 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 α-SMA at approximately 42 kDa. The expected band size for α-SMA is at 42 kDa.
IHC analysis of α-SMA using anti-α-SMA antibody (BM0002).
α-SMA was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0001) with DAB (Catalog # AR1027) as the chromogen.
| 产品名称 | Anti-a-SMA/ACTA2 Antibody (Clone#1A4) |
|---|---|
| 产品编号 | BM0002 |
| 检验物种 | human, mouse, rat |
| 应用范围 | WB, IHC, IF |
| 靶点/蛋白质 | 蛋白质 |
| 反应种属 | 反应种属 |
| 宿主物种 | Mouse |
| 克隆性 | 1A4 |
| 研究领域 | 信号转导 |
| 发货周期 | 现货 |
