Sentence examples for microscopy we recorded from inspiring English sources

Using time-lapse microscopy we recorded images of embryos every 5 minutes for 10 hours.

Using fluorescence time-lapse video microscopy, we recorded the migratory behavior of primitive myeloid cells from their birth.

With total internal reflection fluorescence microscopy, we recorded subplasma membrane concentrations of Ca2+ and ATP ([Ca2+]pm; [ATP]pm) in superficial α- and β-cells of intact islets and related signaling to glucagon and insulin secretion by immunoassay.

By DIC/Nomarksi microscopy, we recorded highly penetrant DTC migration defects in max-2 ; pak-1 double loss-of-function animals compared with few defects in the single mutant.

On the subject of the data obtained by flow cytometry, confocal microscopy, and video microscopy, we were able to record a population of nonphagocytic amoebas for each species and their behavior over time, supporting the results obtained by Sateriale et al. [ 29] who were able to separate amebic subpopulations of E. histolytica with higher and lower rates of phagocytosis.

The images from both devices (Cytoscan A/R and fluorescence microscopy) were recorded on S-VHS video tape (video recorder SVO-9500 MDP, Sony, Koeln, Germany) for later off-line analysis.

By combining whole-cell recording with confocal microscopy we could detect Ca2+ entry into individual spines.

Contrast phase microscopy images, recorded on the four cancer cell lines, exhibit a drastically cell mortality when incubated with 120 μM of SLN− or 84 μM of SLN+.

Atomic-force microscopy (AFM) recorded an average surface roughness of ∼ 21 nm for the coated sample, similar to that of the untreated one (∼ 17 nm).

Importantly, contrast phase microscopy images recorded after incubation of cancer cells in the presence of SLNs at high concentration in sorafenib (> 80 μM) revealed a total cancer cell death in all cases.

Platelet morphology determined by light or electron microscopy was recorded as free text.