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. 2013 Sep 24;(335):47–67. doi: 10.3897/zookeys.335.5490

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