Invitation to tender: Acquisition of a cell sorting device for flow cytometric
analysis and sorting of human cells
Based on his clinical presentation, family history and flow cytometric
analysis, the diagnosis of LAD type 1 was established.
immunophenotyping was first developed by immunologists in the late 1960s and early 1970s as a research tool that enabled their study of the immune system.
Increases in regulatory T cells were sustained for 7 to 10 days, and were concomitant with increases in cytometric
markers of activation and increased suppressive capacity.
studies performed on the bone marrow aspirate revealed a prominent population of leukemic promyelocytes with expression of CD13, CD15, CD33, CD56, and CD117.
For example, in a study on PR hormone status, image cytometric
quantitation of PR immunohistochemical staining correlated with disease-free survival; however, visual quantitation of PR immunostaining did not relate to either overall or disease-free survival.
It includes the application of ancillary tools like histologic stains, immunohistochemical localization of antigens, flow cytometric
studies to classify cell types and determine ploidy, and molecular diagnostics to identify gene mutations and rearrangements, and their indications and applications.
To identify the average functional activity, a cytometric
characterization of follicular epithelium was carried out with the cytometric
studies of follicles at different stages of development.
A 68-year-old woman with a bone marrow biopsy positive for kappa monotypic plasma cells (approximately 90% total) and flow cytometric
analysis showing kappa-restricted plasma cells (approximately 17% of total) had unremarkable serum and urine immunofixation electrophoresis (Fig.
The tetra system, for simultaneous identification and enumeration of T, B and NK lymphocytes in whole blood, provides an easy-to-use solution for multicolor flow cytometric
analysis of lymphocyte subsets, as well as CD4+ and CD8+ T cell subsets ratios.
Presence of macrophages around the beta cells in the pancreas and in the spleen was evaluated by state-of-the-art flow cytometric
technology allowing evaluation on a single cell level.
A variety of detergents and enzymes including saponin, TritonX-100, Tween-20, NP40, Proteinase K and streptolysin 0 were used to optimize a protocol of permeab-ilization for the flow cytometric
enumeration of intracellular 185 rRNA.