Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 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. |
Figure 1. Western blot analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human RT4 whole cell lysates,
Lane 2: human A431 whole cell lysates,
Lane 3: human HepG2 whole cell lysates,
Lane 4: human Hacat whole cell lysates,
Lane 5: human MCF-7 whole cell lysates,
Lane 6: human U20S whole cell lysates,
Lane 7: human Hela whole cell lysates,
Lane 8: human PC-3 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat RH35 whole cell lysates,
Lane 11: mouse liver tissue lysates,
Lane 12: mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ZO-2/TJP2 antigen affinity purified polyclonal antibody (BA2861) 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 ZO-2/TJP2 at approximately 150 kDa. The expected band size for ZO-2/TJP2 is at 134 kDa.
Figure 2. IHC analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861) .
ZO-2/TJP2 was detected in a paraffin-embedded section of human intestinal cancer tissue. The tissue section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IF analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861).
ZO-2/TJP2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 4. IF analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861).
ZO-2/TJP2 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 5. Flow Cytometry analysis of MCF-7 cells using anti-ZO-2/TJP2 antibody (BA2861).
Overlay histogram showing MCF-7 cells stained with BA2861 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) 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 (Red line) was also used as a control.
Figure 1. Western blot analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human RT4 whole cell lysates,
Lane 2: human A431 whole cell lysates,
Lane 3: human HepG2 whole cell lysates,
Lane 4: human Hacat whole cell lysates,
Lane 5: human MCF-7 whole cell lysates,
Lane 6: human U20S whole cell lysates,
Lane 7: human Hela whole cell lysates,
Lane 8: human PC-3 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat RH35 whole cell lysates,
Lane 11: mouse liver tissue lysates,
Lane 12: mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ZO-2/TJP2 antigen affinity purified polyclonal antibody (BA2861) 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 ZO-2/TJP2 at approximately 150 kDa. The expected band size for ZO-2/TJP2 is at 134 kDa.
Figure 2. IHC analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861) .
ZO-2/TJP2 was detected in a paraffin-embedded section of human intestinal cancer tissue. The tissue section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IF analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861).
ZO-2/TJP2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 4. IF analysis of ZO-2/TJP2 using anti-ZO-2/TJP2 antibody (BA2861).
ZO-2/TJP2 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 5. Flow Cytometry analysis of MCF-7 cells using anti-ZO-2/TJP2 antibody (BA2861).
Overlay histogram showing MCF-7 cells stained with BA2861 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ZO-2/TJP2 Antibody (BA2861) 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 (Red line) was also used as a control.