Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-200 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-200 |
ImmunoPrecipitation (IP): | 1:20 |
Figure 1. Western blot analysis of anti-c-Jun/JUN antibody (BM4168). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: human U2OS whole cell lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse Neuro-2a whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Jun/JUN antigen affinity purified monoclonal antibody (BM4168) 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 c-Jun/JUN at approximately 43 kDa. The expected band size for c-Jun/JUN is at 36 kDa.
Figure 2. IF analysis of c-Jun/JUN using anti-c-Jun/JUN antibody (BM4168).
c-Jun/JUN was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-c-Jun/JUN Antibody (BM4168) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 2. IF analysis of c-Jun/JUN using anti-c-Jun/JUN antibody (BM4168).
c-Jun/JUN was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-c-Jun/JUN Antibody (BM4168) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 1. Western blot analysis of anti-c-Jun/JUN antibody (BM4168). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: human U2OS whole cell lysates,
Lane 4: rat C6 whole cell lysates,
Lane 5: mouse Neuro-2a whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Jun/JUN antigen affinity purified monoclonal antibody (BM4168) 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 c-Jun/JUN at approximately 43 kDa. The expected band size for c-Jun/JUN is at 36 kDa.
Figure 2. IF analysis of c-Jun/JUN using anti-c-Jun/JUN antibody (BM4168).
c-Jun/JUN was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-c-Jun/JUN Antibody (BM4168) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 2. IF analysis of c-Jun/JUN using anti-c-Jun/JUN antibody (BM4168).
c-Jun/JUN was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-c-Jun/JUN Antibody (BM4168) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).