The phrase "a thorough cell" is grammatically correct and can be used in written English.
It can be used in contexts discussing biology, research, or any situation where a detailed examination or description of a cell is required.
Example: "In our study, we focused on a thorough cell analysis to understand the underlying mechanisms of cellular function."
Alternatives: "a detailed cell" or "an in-depth cell".
These include the use of high-salt buffers that are not compatible with electroporation conditions and may lead to arcing; the presence of contaminating (unreacted) dye in stock protein samples; and the presence of non-internalized fluorescent molecules that persist in the cell suspension even after thorough cell washing.
The cell pellet was resuspended in guanidine lysis buffer (6 M guanidine hydrochloride, 500 mM sodium chloride, and 20 mM sodium phosphate, pH 7.8) and rocked slowly for 5 to 10 min at room temperature to ensure thorough cell lysis, followed by sonication on ice with three 5-second pulses (high intensity).
Before starting the PMN adhesion assay, the chamber was cleared from remaining blood by a thorough rinse with cell free medium.
In addition, our studies included a thorough analysis of cell type-specific binding patterns, motifs, and nucleosome occupancy of Kaiso sites.
These results beg for a thorough analysis of cell-type specific FMR1 expression patterns and cell-type specific analyses of pathology.
Using intravital videomicroscopy, we performed a thorough examination of cell-trafficking responses within the iris, which is the tissue consistently affected by anterior uveitis.
Following a thorough buffer wash, cells were incubated with a 1 160 000 dilution of mouse monoclonal antibody (G9) followed by a 1 100 dilution of rhodamine red anti-mouse IgG to label γ-tubulin, and a 1 100 dilution of rat monoclonal anti-α-tubulin followed by a 1 100 dilution of fluorescein anti-rat IgG to label microtubules.
In the present study we analyzed the urinary cellular profile of patients with SLE, DN and AAV for T cells and their subsets, B cells and macrophages in order to obrain a thorough view of urinary cells in SLE, and further refine their diagnostic value as biomarkers for LN.
Here, we undertake a thorough analysis of ExEn cell lines to help refine the list of markers that define various endodermal cell types.
A thorough understanding of the cell sensory toolbox might allow the development of engineered tissues or the maintenance of cell phenotypes, such as hepatocytes, that are important in drug toxicity screening.
