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 IL6 using anti-IL6 antibody (BA4339). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse smooth muscle tissue lysates,
Lane 2: mouse heart tissue lysates,
Lane 3: mouse lung tissue lysates,
Lane 4: mouse brain tissue lysates,
Lane 5: mouse small intestine tissue lysates,
Lane 6: mouse Hepa1/6 whole cell lysates,
Lane 7: mouse NIH/3T3 whole cell lysates,
Lane 8: mouse SP/20 whole cell lysates,
Lane 9: mouse RAW264.7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IL6 antigen affinity purified polyclonal antibody (BA4339) 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 IL6 at approximately 30 kDa. The expected band size for IL6 is at 24 kDa.
Figure 2. Western blot analysis of IL6 using anti-IL6 antibody (BA4339). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat smooth muscle tissue lysates,
Lane 2: rat heart tissue lysates,
Lane 3: rat lung tissue lysates,
Lane 4: mouse small intestine tissue lysates,
Lane 5: rat PC-12 whole cell lysates,
Lane 6: rat NRK whole cell lysates,
Lane 7: rat RH-35 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IL6 antigen affinity purified polyclonal antibody (BA4339) 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 IL6 at approximately 30 kDa. The expected band size for IL6 is at 24 kDa.
Figure 3. IHC analysis of IL6 using anti-IL6 antibody (BA4339) .
IL6 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-IL6 Antibody (BA4339) 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 1. Western blot analysis of IL6 using anti-IL6 antibody (BA4339). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse smooth muscle tissue lysates,
Lane 2: mouse heart tissue lysates,
Lane 3: mouse lung tissue lysates,
Lane 4: mouse brain tissue lysates,
Lane 5: mouse small intestine tissue lysates,
Lane 6: mouse Hepa1/6 whole cell lysates,
Lane 7: mouse NIH/3T3 whole cell lysates,
Lane 8: mouse SP/20 whole cell lysates,
Lane 9: mouse RAW264.7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IL6 antigen affinity purified polyclonal antibody (BA4339) 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 IL6 at approximately 30 kDa. The expected band size for IL6 is at 24 kDa.
Figure 2. Western blot analysis of IL6 using anti-IL6 antibody (BA4339). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat smooth muscle tissue lysates,
Lane 2: rat heart tissue lysates,
Lane 3: rat lung tissue lysates,
Lane 4: mouse small intestine tissue lysates,
Lane 5: rat PC-12 whole cell lysates,
Lane 6: rat NRK whole cell lysates,
Lane 7: rat RH-35 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IL6 antigen affinity purified polyclonal antibody (BA4339) 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 IL6 at approximately 30 kDa. The expected band size for IL6 is at 24 kDa.
Figure 3. IHC analysis of IL6 using anti-IL6 antibody (BA4339) .
IL6 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-IL6 Antibody (BA4339) 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.