WB
Western blot analysis of P0/MPZ using anti-P0/MPZ . 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.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-P0/MPZ 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 P0/MPZ at approximately 22 kDa. The expected band size for P0/MPZ is at 22 kDa.
IHC
IHC analysis of P0/MPZ using anti-P0/MPZ .P0/MPZ was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-P0/MPZ 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 P0/MPZ using anti-P0/MPZ .P0/MPZ was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-P0/MPZ at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IF
IF analysis of P0/MPZ using anti-P0/MPZ antibody .P0/MPZ was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-P0/MPZ Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody was used as secondary antibody. The section was counterstained with DAPI .
IF
IF analysis of P0/MPZ using anti-P0/MPZ antibody .P0/MPZ was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-P0/MPZ Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody was used as secondary antibody. The section was counterstained with DAPI .