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. |
Figure 1. Western blot analysis of ATF2 using anti-ATF2 antibody (BA0653). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: HEPG2 whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: SH-SY5Y whole cell lysates,
Lane 5: U-87MG whole cell lysates,
Lane 6: A549 whole cell lysates,
Lane 7: MOLT4 whole cell lysates,
Lane 8: HEL whole cell lysates,
Lane 9: rat brain tissue lysates,
Lane 10: rat thymus tissue lysates,
Lane 11: mouse brain tissue lysates,
Lane 12: mouse thymus tissue lysates,
Lane 13: Neuro-2a whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATF2 antigen affinity purified polyclonal antibody (BA0653) 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 ATF2 at approximately 65-75 kDa. The expected band size for ATF2 is at 55 kDa.
Figure 2. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of rat brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of mouse brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 1. Western blot analysis of ATF2 using anti-ATF2 antibody (BA0653). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: HEPG2 whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: SH-SY5Y whole cell lysates,
Lane 5: U-87MG whole cell lysates,
Lane 6: A549 whole cell lysates,
Lane 7: MOLT4 whole cell lysates,
Lane 8: HEL whole cell lysates,
Lane 9: rat brain tissue lysates,
Lane 10: rat thymus tissue lysates,
Lane 11: mouse brain tissue lysates,
Lane 12: mouse thymus tissue lysates,
Lane 13: Neuro-2a whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATF2 antigen affinity purified polyclonal antibody (BA0653) 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 ATF2 at approximately 65-75 kDa. The expected band size for ATF2 is at 55 kDa.
Figure 2. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of rat brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of ATF2 using anti-ATF2 antibody (BA0653).
ATF2 was detected in a paraffin-embedded section of mouse brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATF2 Antibody (BA0653) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.