WB
Various lysates were subjected to SDS PAGE followed by western blot with CYPA antibody at dilution of 1:20000 incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with HRP-conjugated GAPDH Monoclonal antibody as loading control.
ICC/IF
Immunofluorescent analysis of (-20°C Methanol) fixed HeLa cells using Cyclophilin A antibody at dilution of 1:400 and Omnimabs® 488 Goat Anti-Mouse IgG(H&L).
FC
1X10^6 HeLa cells were intracellularly stained with 0.4 ug Anti-Human Cyclophilin A and Omnimabs® 488 Goat Anti-Mouse IgG(H&L) at dilution 1:1000 (red), or 0.4 ug Mouse IgG1 Isotype Control (blue). Cells were fixed with 4% PFA and permeabilized with Flow Cytometry Perm Buffer.