WB
Western blot analysis of EEF1A1A/1B using anti-EEF1A1A/1B . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: zebrafish head tissue lysates,Lane 2: whole female zebrafish tissue lysates,Lane 3: whole male zebrafish tissue lysates,Lane 4: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EEF1A1A/1B antigen affinity purified polyclonal at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary . The signal is developed using ECL Plus Western Blotting Substrate . A specific band was detected for EEF1A1A/1B at approximately 50 kDa. The expected band size for EEF1A1A/1B is at 50 kDa.
IHC
IHC analysis of EEF1A1A/1B using anti-EEF1A1A/1B .EEF1A1A/1B was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-EEF1A1A/1B 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 EEF1A1A/1B using anti-EEF1A1A/1B .EEF1A1A/1B was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-EEF1A1A/1B 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 EEF1A1A/1B using anti-EEF1A1A/1B .EEF1A1A/1B was detected in a paraffin-embedded section of zebrafish skeletal muscle tissue. The tissue section was incubated with rabbit anti-EEF1A1A/1B at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.