Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (IF): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
(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 Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004). 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 A431 whole cell lysates,
Lane 3: human RT4 whole cell lysates,
Lane 4: human T-47D whole cell lysates,
Lane 5: human A549 whole cell lysates,
Lane 6: human PC-3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Beta Catenin/CTNNB1 antigen affinity purified polyclonal antibody (A00004) 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 Beta Catenin/CTNNB1 at approximately 95 kDa. The expected band size for Beta Catenin/CTNNB1 is at 85 kDa.
Figure 2. Western blot analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: rat C6 whole cell lysates,
Lane 3: rat RH-35 whole cell lysates,
Lane 4: mouse brain tissue lysates,
Lane 5: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Beta Catenin/CTNNB1 antigen affinity purified polyclonal antibody (A00004) 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 Beta Catenin/CTNNB1 at approximately 95 kDa. The expected band size for Beta Catenin/CTNNB1 is at 85 kDa.
Figure 3. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 4. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human colon cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 5. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 6. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of mouse small intestine tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 7. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of rat small intestine tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 8. IF analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human intestine cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 9. IF analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 10. Flow Cytometry analysis of Hela cells using anti-Beta Catenin/CTNNB1 antibody (A00004).
Overlay histogram showing Hela cells stained with A00004 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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.
Figure 1. Western blot analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004). 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 A431 whole cell lysates,
Lane 3: human RT4 whole cell lysates,
Lane 4: human T-47D whole cell lysates,
Lane 5: human A549 whole cell lysates,
Lane 6: human PC-3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Beta Catenin/CTNNB1 antigen affinity purified polyclonal antibody (A00004) 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 Beta Catenin/CTNNB1 at approximately 95 kDa. The expected band size for Beta Catenin/CTNNB1 is at 85 kDa.
Figure 2. Western blot analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: rat C6 whole cell lysates,
Lane 3: rat RH-35 whole cell lysates,
Lane 4: mouse brain tissue lysates,
Lane 5: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Beta Catenin/CTNNB1 antigen affinity purified polyclonal antibody (A00004) 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 Beta Catenin/CTNNB1 at approximately 95 kDa. The expected band size for Beta Catenin/CTNNB1 is at 85 kDa.
Figure 3. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 4. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human colon cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 5. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 6. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of mouse small intestine tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 7. IHC analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of rat small intestine tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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 8. IF analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in a paraffin-embedded section of human intestine cancer tissue. The tissue section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 9. IF analysis of Beta Catenin/CTNNB1 using anti-Beta Catenin/CTNNB1 antibody (A00004).
Beta Catenin/CTNNB1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 10. Flow Cytometry analysis of Hela cells using anti-Beta Catenin/CTNNB1 antibody (A00004).
Overlay histogram showing Hela cells stained with A00004 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Beta Catenin/CTNNB1 Antibody (A00004) 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.