Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Flow cytometry (FCM): | 1-3 μg/1x106 cells |
(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 Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat liver tissue lysates,
Lane 2: mouse liver tissue lysates,
Lane 3: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 8/CASP8 antigen affinity purified polyclonal antibody (A00042) 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 Caspase 8/CASP8 at approximately 55 kDa. The expected band size for Caspase 8/CASP8 is at 55 kDa.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of mouse spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of rat intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of rat spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of PC-3 cells using anti-CASP8 antibody (A00042).Overlay histogram showing PC-3 cells stained with A00042 (Blue line).. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Flow Cytometry analysis of Hela cells using anti-CASP8 antibody (A00042).Overlay histogram showing Hela cells stained with A00042 (Blue line).. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Western blot analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat liver tissue lysates,
Lane 2: mouse liver tissue lysates,
Lane 3: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 8/CASP8 antigen affinity purified polyclonal antibody (A00042) 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 Caspase 8/CASP8 at approximately 55 kDa. The expected band size for Caspase 8/CASP8 is at 55 kDa.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of mouse spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of rat intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of rat spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Caspase 8/CASP8 using anti-Caspase 8/CASP8 antibody (A00042).
Caspase 8/CASP8 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Caspase 8/CASP8 Antibody (A00042) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of PC-3 cells using anti-CASP8 antibody (A00042).Overlay histogram showing PC-3 cells stained with A00042 (Blue line).. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Flow Cytometry analysis of Hela cells using anti-CASP8 antibody (A00042).Overlay histogram showing Hela cells stained with A00042 (Blue line).. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.