Table 2. Possible artifacts in cases of different sample structures.
Star | Array | Vesicles | Lines | Solution(s) | |
---|---|---|---|---|---|
High labeling density | − Clustering effect [39] − Increased number of rejected localizations [37] |
False structure caused by the overlapping | Bridge formation between the individual vesicles | − Low contrast cross-sections [22, 28] − High intensity ends − False lines [15] |
− Reduce concentration − Using unlabelled antibodies too − 1 dye/antibody − Increase the frame-rate |
Low labeling density | Low contrast | Not enough information about the structures | − under-sampling − false distance measurement |
Structured lines with hot spots [29] | − Increase concentration − Capture more frame |
Defocus | Blurred edges | Low lateral resolution | − Low contrast image − Blurred image − High localization error |
Blurred image | Usage of autofocus system |
Long linker | Unshaped edges | False or vanished structure | False distance measurement | False structure (parallel lines instead of single one) | − Nanobody − Direct labeling |