Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of anti-MT-CO1 antibody (BA2149-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HeLa mitochondria lysates at 20ug,
Lane 2: human HeLa whole cell lysates at 20ug,
Lane 3: human Caco-2 whole cell lysates at 50ug,
Lane 4: rat heart tissue lysates at 50ug.
Lane 5: mouse heart tissue lysates at 50ug.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MT-CO1 antigen affinity purified polyclonal antibody (BA2149-2) 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 MT-CO1 at approximately 37 kDa. The expected band size for MT-CO1 is at 57 kDa.
IHC analysis of MT-CO1 using anti-MT-CO1 antibody (BA2149-2).
MT-CO1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
ICC analysis of MT-CO1 using anti-MT-CO1 antibody (BA2149-2).
MT-CO1 was detected in an immunocytochemical section of C6 cells. The section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of anti-MT-CO1 antibody (BA2149-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HeLa mitochondria lysates at 20ug,
Lane 2: human HeLa whole cell lysates at 20ug,
Lane 3: human Caco-2 whole cell lysates at 50ug,
Lane 4: rat heart tissue lysates at 50ug.
Lane 5: mouse heart tissue lysates at 50ug.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MT-CO1 antigen affinity purified polyclonal antibody (BA2149-2) 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 MT-CO1 at approximately 37 kDa. The expected band size for MT-CO1 is at 57 kDa.
IHC analysis of MT-CO1 using anti-MT-CO1 antibody (BA2149-2).
MT-CO1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
ICC analysis of MT-CO1 using anti-MT-CO1 antibody (BA2149-2).
MT-CO1 was detected in an immunocytochemical section of C6 cells. The section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.