Western blot analysis of MTA1 using anti-MTA1 antibody (BA2749). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human MCF-7 whole cell lysates,
Lane 2: human HEK293 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: human PC-3 whole cell lysates,
Lane 5: human Raji whole cell lysates,
Lane 6: human K562 whole cell lysates,
Lane 7: rat brain tissue lysates,
Lane 8: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MTA1 antigen affinity purified polyclonal antibody (BA2749) 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 MTA1 at approximately 80 kDa. The expected band size for MTA1 is at 80 kDa.
IHC analysis of MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human rectal cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human pancrease cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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.
| Western blot (WB): | 1:500-2000 |
| Immunohistochemistry (IHC): | 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 MTA1 using anti-MTA1 antibody (BA2749). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human MCF-7 whole cell lysates,
Lane 2: human HEK293 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: human PC-3 whole cell lysates,
Lane 5: human Raji whole cell lysates,
Lane 6: human K562 whole cell lysates,
Lane 7: rat brain tissue lysates,
Lane 8: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MTA1 antigen affinity purified polyclonal antibody (BA2749) 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 MTA1 at approximately 80 kDa. The expected band size for MTA1 is at 80 kDa.
IHC analysis of MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human rectal cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human pancrease cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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.
Western blot analysis of MTA1 using anti-MTA1 antibody (BA2749). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human MCF-7 whole cell lysates,
Lane 2: human HEK293 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: human PC-3 whole cell lysates,
Lane 5: human Raji whole cell lysates,
Lane 6: human K562 whole cell lysates,
Lane 7: rat brain tissue lysates,
Lane 8: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MTA1 antigen affinity purified polyclonal antibody (BA2749) 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 MTA1 at approximately 80 kDa. The expected band size for MTA1 is at 80 kDa.
IHC analysis of MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human rectal cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in frozen section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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 MTA1 using anti-MTA1 antibody (BA2749) .
MTA1 was detected in a paraffin-embedded section of human pancrease cancer tissue. The tissue section was incubated with rabbit anti-MTA1 Antibody (BA2749) 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.
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