CDA Mouse mAb (Ab095561) - Western Blot All lanes: CDA Mouse mAb (Ab095561) at 1/1000 dilution Samples: Lysates at 20 µg per lane Secondary: Goat Anti-Mouse IgG H&L (HRP) (Ab179001) at 1/20000 dilution
Predicted band size: 16 kDa Observed band size: 16 kDa Exposure time: 15.0 s
CDA Mouse mAb (Ab095561) - IHC IHC-P was performed using sections of the formalin-fixed paraffin-embedded spleen tissue. Antigen was retrieved through addition of boiling Tris/EDTA buffer pH 9 in a pressure cooker for 3 min. Endogenous peroxidase activity was quenched by incubating the sections with 3% H2O2 for 30 min at room temperature. The sections were then incubated with CDA Mouse mAb (Ab095561) at 2.5 µg/mL at room temperature for 1 h. Poly-peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. Diaminobenzidine was used as the chromogen. The section was counterstained with hematoxylin. A tissue section incubated with phosphate-buffered saline followed by incubation with the secondary antibody was used as the background control. Result: Cells in red pulp are positively stained.
CDA Mouse mAb (Ab095561) - IP Immunoprecipitation was performed by incubation of 2.5 µg CDA Mouse mAb (Ab095561) with SK-OV-3 lysate containing 200 µg total protein. After absorption with Protein G beads, the mixture was run on 6-18% SDS-PAGE and blotted onto nitrocellulose membrane. CDA Mouse mAb (Ab095561) at 1 µg/mL was used as the primary antibody and peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. Lane 1: SK-OV-3 lysate Lane 2: CDA immunoprecipitated from SK-OV-3 lysate by CDA Mouse mAb (Ab095561) Lane 3: The same as Lane 2 but Mouse IgG was used as IgG isotype control antibody Result: CDA Mouse mAb (Ab095561) can immunoprecipitate CDA.