ImmunofluorescenceWT MEF cells (WASH +/+) or WASHout MEF cells (WASH-/-) were fixed in 4% PFA for 20 minutes and permeabilized with 0.15% Surfactamps for 3 minutes. Fixed cells were stained with 1:300 dilution of Monoclonal Anti-WASH1 Clone: WASH1-27 (
Cat. No. SAB4200552). The antibody was developed using Goat Anti-Mouse IgG, TRITC conjugate. Cells were counterstained with Hoechst (blue) to stain nuclei. Pictures are courtesy of Timothy S. Gomez and Daniel D. Billadeau, Departments of Biochemistry and Molecular Biology and Immunology, Division of Oncology Research, Mayo Clinic, Rochester, USA.
ImmunoblottingWhole extract of HEK-293T cells overexpressing mouse WASH1 was separated on SDS-PAGE and probed with Monoclonal Anti-WASH1 Clone: WASH1-27 (
Cat. No. SAB4200552). The antibody was developed using Goat Anti-Mouse IgG-Peroxidase (
Cat. No. A2304) and a chemiluminescent substrate.
Lanes1. 2 μg/mL antibody
2. 5 μg/mL antibody
3. 5 μg/mL antibody + WASH1 immunizing peptide
ImmunoblottingWhole extracts of WT MEF cells (WASH +/+) or WASHout MEF cells (WASH-/-) were separated on SDS-PAGE and probed with 1:1,000 dilution of Monoclonal Anti-WASH1 Clone: WASH1-27 (
Cat. No. SAB4200552). The antibody was developed using Goat Anti-Mouse IgG-Peroxidase and a chemiluminescent substrate. The picture is courtesy of Timothy S. Gomez and Daniel D. Billadeau, Departments of Biochemistry and Molecular Biology and Immunology, Division of Oncology Research, Mayo Clinic, Rochester, USA.
ImmunoprecipitationMonoclonal Anti-WASH1 Clone: WASH1-27 (
Cat. No. SAB4200552) was used to immunoprecipitate WASH1 from HeLa whole cell extract. Detection antibody: Rabbit Anti-WASH1 (
Cat. No. SAB4200372).
Lanes1. 5 μg antibody
2. 10 μg antibody
3. Negative control: 10 μg non-relevant antibody