Sentence examples for air objectives from inspiring English sources

Epifluorescence images were taken with ×4 and ×10 air objectives (NA 0.1 and 0.25, respectively).

The objectives used were UPlanFI 4 × NA 0.13, LCPlanFI 20 × NA 0.40 (all air objectives) and Zeiss EC Plan Neoflur 20 × 0.5NA objectives.

Confocal imaging was performed using an inverted laser scanning microscope (IX81 model FV1000; Olympus, Melville, NY, USA) with ×20 and ×40 air objectives.

The sample is illuminated by a femtosecond pulsed Ti Sapphire laser, directed to the sample by a dichroic mirror (HFT KP650) and through a Zeiss 20x Plan-APOCHROMAT or a 40x LD ACHROPLAN air objectives.

Embryos stained with NBT/BCIP were mounted in 87% Glycerol on microscope slides and imaged with a Leica DM5000B, 10x or 20x air objectives, Leica CD500 microscope camera and Leica FireCam 1.7.1 software.

Imaging was performed as described previously using the Zeiss LSM510 (Auffray et al., 2007 ), or using 10 × 0.4 N.A. HCX PL APO and 20 x 0.5 N.A PL Fluotar air objectives on the Leica SP5 with 488 and 561nm laser lines for GFP and PE respectively.

General nuclear staining (DAPI) and Alexa 594 were serially detected in nine fields per well using a ×20 air objective.

Olympus 10× UPlanFL N 0.3 NA air objective was used for sample alignment and large field of view fluorescence imaging.

Pictures were taken every 5 min for 24 h for migration of MCF10A and for 48 h for MCF10A-FUCCI using the Plan-Apochromat 20×/0.80 air objective.

Three-dimensional z-stacks were collected using a 20X/0.8 N.A. air objective at step-size of 1.0 2.0 μm and 1024×1024 resolution.

Living HeLa and RPE-1 (hTERT) cells were imaged using an ImageXpress Micro XLS widefield screening microscope (Molecular Devices) equipped with a 20 × /0.7, air objective (Nikon) and a laser‐based autofocus.