IF
IF analysis of SMARCA4A using anti-SMARCA4A antibody .SMARCA4A was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-SMARCA4A Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody was used as secondary antibody.
WB
Western blot analysis of SMARCA4A using anti-SMARCA4A antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SMARCA4A 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 SMARCA4A at approximately 220 kDa. The expected band size for SMARCA4A is at 185 kDa.
IHC
IHC analysis of SMARCA4A using anti-SMARCA4A antibody .SMARCA4A was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-SMARCA4A 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 SMARCA4A using anti-SMARCA4A antibody .SMARCA4A was detected in a paraffin-embedded section of zebrafish spinal cord tissue. The tissue section was incubated with rabbit anti-SMARCA4A 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 SMARCA4A using anti-SMARCA4A antibody .SMARCA4A was detected in a paraffin-embedded section of zebrafish eye tissue. The tissue section was incubated with rabbit anti-SMARCA4A Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.