Table 2.
Microscope lens and confocal laser scanning microscopy (CLSM) settings used for the observation of the specimens; Ch1 and Ch2 = detection channels 1 and 2.
| Lens | HC PL APO CS (High-grade colour-corrected Plan Apochromat lens for confocal) |
|---|---|
| Objective | 20× |
| Numerical aperture | 0.7 |
| Immersion | Oil |
| Excitation wavelength | 488 and 633 nm |
| Laser intensity | 50% and 33%, respectively |
| Excitation beam splitter | TD 488/561/633 |
| Detected emission wavelength | Ch1: 493 – 600 nm |
| Ch2: 650 – 750 nm | |
| Detector gain | 833.8 and 791.6 V |
| Amplitude offset | -0.9 and -1.0 % |
| Electronic zoom | 3X |
| Pinhole aperture | 54.6 μm |
| Image format | 2048 × 2048 dpi |