Western blot analysis of APOC3 using anti-APOC3 antibody (PB1097). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates.
\After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-APOC3 antigen affinity purified polyclonal antibody (PB1097) 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 APOC3 at approximately 12-14 kDa. The expected band size for APOC3 is at 11 kDa.
IHC analysis of APOC3 using anti-APOC3 antibody (PB1097) .
APOC3 was detected in a paraffin-embedded section of mouse liver tissue. The tissue section was incubated with rabbit anti-APOC3 Antibody (PB1097) 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.
Flow Cytometry analysis of HepG2 cells using anti-APOC3 antibody (PB1097).
Overlay histogram showing HepG2 cells stained with PB1097 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-APOC3 Antibody (PB1097) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
| Western blot (WB): | 1:500-2000 |
| Immunohistochemistry (IHC): | 1:50-400 |
| Flow Cytometry (Fixed): | 1:50-200 |
| (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 APOC3 using anti-APOC3 antibody (PB1097). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates.
\After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-APOC3 antigen affinity purified polyclonal antibody (PB1097) 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 APOC3 at approximately 12-14 kDa. The expected band size for APOC3 is at 11 kDa.
IHC analysis of APOC3 using anti-APOC3 antibody (PB1097) .
APOC3 was detected in a paraffin-embedded section of mouse liver tissue. The tissue section was incubated with rabbit anti-APOC3 Antibody (PB1097) 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.
Flow Cytometry analysis of HepG2 cells using anti-APOC3 antibody (PB1097).
Overlay histogram showing HepG2 cells stained with PB1097 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-APOC3 Antibody (PB1097) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Western blot analysis of APOC3 using anti-APOC3 antibody (PB1097). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates.
\After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-APOC3 antigen affinity purified polyclonal antibody (PB1097) 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 APOC3 at approximately 12-14 kDa. The expected band size for APOC3 is at 11 kDa.
IHC analysis of APOC3 using anti-APOC3 antibody (PB1097) .
APOC3 was detected in a paraffin-embedded section of mouse liver tissue. The tissue section was incubated with rabbit anti-APOC3 Antibody (PB1097) 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.
Flow Cytometry analysis of HepG2 cells using anti-APOC3 antibody (PB1097).
Overlay histogram showing HepG2 cells stained with PB1097 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-APOC3 Antibody (PB1097) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
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