Examples of 'cells were determined' in a sentence
Meaning of "cells were determined"
cells were determined: Indicates that specific cells were identified, analyzed, or planned for a particular purpose, such as in scientific research or medical treatment
How to use "cells were determined" in a sentence
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cells were determined
Apoptotic cells were determined by using TdT staining.
Cytotoxicities of the effector cells were determined.
The number of viable cells were determined by direct counting on a hemacytometer.
The fatty acid and chitin contents of sporulating Hansenula anomala cells were determined.
Percentages of positive cells were determined as described below.
Levels of haematocrit, haemoglobin and red blood cells were determined.
The number of infiltrating cells were determined using a coulter counter.
Having defined the optimal conditions, the types and percentages of transfected cells were determined.
The percentages of apoptotic cells were determined by flow cytometry.
Viable cells were determined by Trypan blue dye exclusion and counted in an hemocytometer.
The percentages of undifferentiated cells were determined in two days increments.
After thorough investigations, the anti-proliferative effects of the samples on breast cancer cells were determined.
Morphology and growth behavior of cells were determined by optical control.
The number of cells were determined by inspection with the naked eye 18 days after plating.
Subpopulations of leukocytes and red blood cells were determined from the whole blood sample.
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Viable cells were determined after 5 days of culture by XTT.
The number and the viability of the cells were determined by trypan blue staining.
The cells were determined to be free of mycoplasma and rodent viruses ( MAP testing ).
Cell cycle arrest and numbers of dead cells were determined using propidium iodine staining.
Apoptotic cells were determined as Annexin V positive, propidium iodide negative cells by FACS analysis.
Levels of circulating Pmel cells were determined by flow cytometry.
On day 3, total cell number and hemoglobin containing ( benzidine positive ) cells were determined.
Percentages of stained cells were determined and compared to the appropriate negative controls.
Serum antibodies to formalin inactivated ETEC whole cells were determined by the ELISA method.
Thus, these cells were determined to be hybridomas.
Total cellular RNA concentrations present in samples from transfected BHK cells were determined spectrophotometrically.
The ApoE amounts in the cells were determined by the method described above.
Mean channel fluorescence intensity ( MFI ) and percentage of positive cells were determined for each sample.
Proliferation of spleen cells were determined in accordance with the method of Byars et al.
The caspase-3 activities of the collected cells were determined.
Levels of circulating Pmel cells were determined by flow cytometry of blood samples.
The total cell number and the percentage of hemoglobin-containing cells were determined after 14 days.
Yields per million seeded cells were determined with an EPO ELISA on supernatants from PER.
Cytokine ( pg / mL ) levels in culture supernatants of spleen cells were determined by ELISA assay.
Concentrations applied to cells were determined considering several parameters, such as.
As in the above section 2, CC50 values for MDCK cells were determined.
The apoptotic cells were determined using a Becton-Dickinson FACScan cytometer.
The radioactivity of ³ H-Thymidine incorporated into the cells were determined by a scintillation counter.
IFN-Y secreting cells were determined by ELISpot assay as described above.
The proliferative capacity of antigen-specific T cells were determined by CFSE staining.
However, CD11c cells were determined in peritoneal fluid by flow cytometry.
To monitor loss of biological activity, EC50 values in IMR90 cells were determined.
The cell counts and the percentage of viable cells were determined using a hemocytometer Neubauer chamber.
Dead cells were determined by fluorimetric analysis ( staining with propidium iodide ( PI ) ).
The CBFs of six different cells were determined over a period of 1 min.
Aliquots were removed each week and the EC50 values in IMR90 cells were determined.
The otm and the number of trap-positive cells were determined by histopathological analysis.
The migrated cells were determined with a fluorescent plate reader ( LJL BioSystems, Sunnyvale, CA ).
The levels of biotCXCL8 binding to the cells were determined using ELISA technology.
The responding cells were determined by the use of a Domino Image Analyzer ( Otpomax, Hollis, NH ).
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Examples of using Cells
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For cells or batteries packed with equipment
They were beaten in the cells or in the courtyard
The cells we want can not be tainted
