WB
Western blot analysis of CYP3A65 using anti-CYP3A65 antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: whole female zebrafish tissue lysates,Lane 2: whole male zebrafish tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CYP3A65 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 . A specific band was detected for CYP3A65 at approximately 59 kDa. The expected band size for CYP3A65 is at 59 kDa.
IHC
IHC analysis of CYP3A65 using anti-CYP3A65 antibody .CYP3A65 was detected in a paraffin-embedded section of zebrafish ovary tissue. The tissue section was incubated with rabbit anti-CYP3A65 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 CYP3A65 using anti-CYP3A65 antibody .CYP3A65 was detected in a paraffin-embedded section of zebrafish eye tissue. The tissue section was incubated with rabbit anti-CYP3A65 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 CYP3A65 using anti-CYP3A65 antibody .CYP3A65 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-CYP3A65 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 CYP3A65 using anti-CYP3A65 antibody .CYP3A65 was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-CYP3A65 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.