WB
Western blot analysis of FCER1G using anti-FCER1G antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FCER1G antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
IHC
IHC analysis of FCER1G using anti-FCER1G antibody.
FCER1G was detected in a paraffin-embedded section of human spleen tissue. The tissue section was incubated with rabbit anti-FCER1G Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of FCER1G using anti-FCER1G antibody.
FCER1G was detected in a paraffin-embedded section of mouse spleen tissue. The tissue section was incubated with rabbit anti-FCER1G Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of FCER1G using anti-FCER1G antibody.
FCER1G was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-FCER1G Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IP
IP analysis of FCER1G using anti-FCER1G antibody in HEL whole cell lysate.
Western blot analysis of FCER1G using anti- FCER1G antibody.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti- FCER1G antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.