Sentence examples for microscopy we compared from inspiring English sources

Using electron microscopy, we compared the ultra-structural features of haustoria developed in Te-0 and Col-0 plants.

By using time-lapse microscopy, we compared frequency of re-orientation of GFP-marked unreplicated monocentrics between different YFP-labeled SPBs in MPS1+ and mps1-as1 cells.

With SRS microscopy, we compared the lignin concentrations in different cell wall layers, e.g., the cell corner, compound middle lamella, and secondary wall, both untreated and treated at various maleic acid concentrations.

Using serial section electron microscopy, we compared the neuropil from the chemically fixed brains with tissue samples that had been rapidly excised and cryo fixed using high-pressure freezing (McDonald and Auer, 2006) and resin embedded by freeze substitution (Sosinsky et al., 2008).

Using light microscopy and scanning electron microscopy we compared key developmental features of laser-manipulated and control samples, including the olfactory pit, dorsal, ventral and pectoral fins, notochord, pectoral fin buds, otic capsule, otic vesicle, neuromast patterning, and kinocilia of the olfactory pit rim and cristae of the lateral wall of the ear.

Using in-situ scanning tunnelling microscopy, we compare the Ni/Au(111) electrochemical epitaxy on reconstructed and on unreconstructed Au(111).

To evaluate the performance of CARS microscopy, we compare CARS imaging assays with standard dye-labeled assays to quantitate fat stores.

Utilizing immunofluorescence tagging and microscopy, we next compared cells expressing PrPWt, PrPT183A and PrPF198S by immunostaining with 1E4 or 3F4.

In the first set of experiments performed using filter retardation assay (FRA), western blot (WB) and high-resolution fluorescence microscopy (HRFM) analysis, we compared the effects of single treatments with Bicalutamide or trehalose on ARpolyQ aggregation and clearance in the absence of or in the presence of testosterone (to trigger the formation of ARpolyQ toxic species) in NSC34 cells.

In order to confirm that T-tubules are within the Z-T band we compared CARS microscopy data taken for Raman shift frequencies that are close and away from the symmetric stretch CH2 vibration line that is characteristic for lipids.

In this study we compared three electron microscopy techniques to determine retroviral titre in bulk harvest.