Sentence examples for microscopy by taking from inspiring English sources

(D) Live confocal microscopy by taking images from a series of different regions started with time after the addition of Abs, generally 50 observations during the 90 min period.

Increasing the sensitivity of microscopy by taking multiple measurements may reduce the number of true cases wrongly classified as non-infected by microscopy.

The deflections are measured precisely by atomic force microscopy (AFM) by taking AgOx and ZnS SiO2 as the active layer and nanofilm, respectively, and by controlling pulse laser parameters.

This includes microscopy techniques like confocal microscopy [11] and multiphoton microscopy [12] that section tissue by taking 2D images at different depths through the sample, as well as optical techniques that are tomographic, like optical projection tomography (OPT) [13] and electron tomography [14] that use 2D projections at many different angles to create a 3D dataset.

We obtained the out-of-focus TPEF signals of 3.85 × 10−3 and 3.79 × 10−5 for conventional TPEF microscopy and SPOMNOM, respectively, by taking the averages of TPEF intensities at axial positions from 40 μm to 80 μm.

We obtained the out-of-focus SFG signals of 3.44 × 10−3 and 3.43 × 10−5 for conventional SFG microscopy and SPOMNOM, respectively, by taking the averages of SFG intensities at axial positions from −40 μm to −20 μm.

The size homogeneity of the resin beads was determined by taking optical microscopy images with a Nikon Eclipse TS 100 optical microscope and a Digital camera Cooled MDC Nikon, and measuring the diameter of the beads.

To validate these rules, we first collected experimental data describing growth characteristics of co-cultured HMEC and vHMEC imaged by time-lapse microscopy (note: vHMEC were obtained by taking HMEC that had escaped stasis in a previous experiment).

Several attempts have been made in previous studies to explain the variation of the reflectance values by taking scanning electron microscopy (SEM) images of the texture surface and theoretical modeling of reflectance [7, 14 17].

The schizont mixture was washed in fresh warm medium without C1 and observed by time-lapse DIC microscopy (left), taking images at 5 s intervals.

We imaged SpoIIE during sporulation by structured illumination microscopy, taking advantage of a fluorescent fusion protein to stain the membrane and mark the nascent septum.