The phrase "analysis of sorted" is not complete and lacks clarity in written English.
It could be used in contexts discussing data or information that has been organized or arranged in a specific order, but it needs additional context to be fully understood.
Example: "The analysis of sorted data revealed significant trends that were previously unnoticed."
Alternatives: "examination of ordered" or "evaluation of arranged".
Post-sorting analysis of sorted DC populations showed that purity ranged from 90 99% and the average purity of populations used for stimulation were 98%.
For analysis of sorted cells, cells were counted post-sorting using a Cellometer AutoT4 (Nexcelom Bioscience, Lawrence, MA, USA).
Purity of sorted populations was assessed by analysis of sorted populations by flow cytometry immediately after the sort and also by analysis of DNA content in fixed sorted cells by PI incorporation.
Through microarray analysis of sorted heart progenitor cells, we identified the complete set of primary genes upregulated by FGF/Ets shortly after heart progenitor emergence.
To investigate the molecular mechanisms by which NAP1L3 contributes to human HSC function and haematopoietic differentiation, we performed RNA sequencing (RNA-Seq) and global expression profiling analysis of sorted human UCB HSCs, transduced with shRNA vectors targeting NAP1L3, compared to cells transduced with a negative control vector, 72 hours post transduction of the cells.
An analysis of sorted CCR2− macrophages from nicotine-treated mice confirmed significantly higher levels of active translation for the M2-related genes IL-10 and Arg1 than were found in sorted macrophages from normal, injured, or locally ISO-treated corneas (Fig. 7e, bottom; factorial-design ANOVA, P < 0.01).
Re-analysis of sorted cells reproducibly demonstrated high purity (>98%).
Purity>90% were confirmed by re-analysis of sorted cells.
In yet another component, we performed clinical hematology counts and pre- and post-sorting flow cytometric analysis of the sorted cell populations to measure the clinical relevance and efficiency of the experimental sampling conditions.
Further analysis of the sorted cell population using electron microscopic analysis revealed the sorted CD31+CD45− cells lacked distinctive nuclei and contain open canalicular systems (OCS), alpha granules, dense bodies and were of the order of 3 5 μm in size, features completely consistent with large, immature platelets.
Gene expression analysis of the sorted tumor cells revealed that the Aldefluor+ tumor cells has decreased expression of transporter associated with antigen processing (TAP) genes and co-stimulatory molecule CD80, which would decrease susceptibility to T cells.
