We tried it in our lab, doing firstly SA-B-gal staining and then IF. But chromogen from SA-B-gal gives very high background and antibodies are loosing their specificity or are unable to bind to epitope. It works very poorly and we were unable to optimalize it. But you can try to stain lipofuscin with Sentragor (marker of senecence) and then stain protein of interest with IF. Good luck!