IF
IF analysis of ATP5G1/2/3 using anti-ATP5G1/2/3 antibody .ATP5G1/2/3 was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-ATP5G1/2/3 Antibody at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody was used as secondary antibody. The section was counterstained with DAPI .
WB
Western blot analysis of ATP5G1/2/3 using anti-ATP5G1/2/3 antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: zebrafish head tissue lysates,Lane 2: female zebrafish viscera tissue lysates,Lane 3: male zebrafish viscera tissue lysates,Lane 4: whole zebrafish tissue lysates,Lane 5: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5G1/2/3 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 ATP5G1/2/3 at approximately 10 kDa. The expected band size for ATP5G1/2/3 is at 10 kDa.
IHC
IHC analysis of ATP5G1/2/3 using anti-ATP5G1/2/3 antibody .ATP5G1/2/3 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-ATP5G1/2/3 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.