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Flow cytometery histogram and dot plot. shows a large population of cells expressing both CD33 and CD34.

Flow cytometric analysis and GFP production of cells in an high cell density fermentation. Samples taken from the fed-batch of B. megaterium WH323 carrying pRBBm56 Accordingly coloured columns show percentage of the subpopulation compared to all cells

Flow cytometric analysis of intracellular Ca i in celecoxib-treated PC-3 cells. Dose- and time-dependent effect of celecoxib on i. lndo-1-loaded PC-3 cells were treated with different levels of celecoxib, ranging from 0 to 100 pM, and were subjected to flow cytometric Ca analysis as described in the Materials and Methods. Source

Flow cytometric analysis of lL-4 and IFNy.

Flow cytometric analysis of MHC class I and II expression. Panel A. Analysis of MHC class I antigens. NOD mice express H-2 Kd and H-2Db MHC class I alleles. They also express l-Ag7 and do not express the l-Ab allele. NOD-sc d IL2ry u mice express the H-2 Kd and H-2Db MHC class I alleles. Expression is duller because of the absence of MHC class l-bright lymphocytes. These mice have low numbers of l-Ag7 expressing cells and lack expression of l-Ab on their cells. NOD-sc d IL2rymllAtful1 mice lack MHC class II expression and exhibit dull H-2Db expression with no expression of H-2 Kd.

Flow cytometric analysis of surface water from points at 1.5 mile intervals off shore from Cape Flatteras, North Carolina. Forward scatter and orange autofluorescence identify two Synechococcus populations with different phycoerythrin content. Beads were used to calibrate the number of cells present. From Chisholm et al. .

Flow cytometric detection of apoptotic cell deadi using the annexin V method after treatment with IgM anti-Fas mAb. The vacant retrovirus vector , whereas only faint annexin V binding is observed in LdelSN-transfected Jurkat cell clone RJ-14. This means diat endogenous wild-type mFas in the LX-2 cells is functional in Fas-mediated apoptosis, but transfected aberrant mFas in die RJ-14 cells interferes with die signaUng in a dominant negative manner.

Flow cytometric differential detergent resistance

Flow cytometric histogram of Flow-Cal 575 Fluorospheres. The fluorescence intensity of light-scatter-gated beads bead population is positioned in the left quarter of the histogram

Flow cytometric histograms showing staining of scatter-gated lymphocytes with BY55 antibody. Histogram axes defined as in

Flow cytometric method does not differentiate between nucleated erythroid cells and reticulocytes, on some instruments. Non-nucleated e throid cells were isolated using cellulose fractionation. Part of the sample was stained with Wright-Giemsa and reticulocytes and mature nucleated cells quantified by trained medical technologists.

Flow cytometric profiles of K.562 cells stained with propidium iodide after 24 li exposure to 100 pM iron-binding-equivalents of CP94 .

Flow cytometric signatures distinguishing three different strains of bacteria according to the size distributions of DNA fragments generated by restriction enzyme digestion. From Kim et al. .

Flow cytometry analyses of BAL T lymphocytes from two HP patients showing the percentage of CD4 and CD8 cells. Chronic former smoker HP patient demonstrating an increase in the CD4 CD8 ratio. Normal values for BAL CD4 CD8 ratio

Flow cytometry analysis of apoptotic cells. HL-60 cells were treated with vehicle alone staining, DNA content was analyzed by FACs laser flow cytometer.

Flow cytometry analysis of cell cycle. HL-60 cells were exposed for 24 h to 3.5 j.M 5b

Flow cytometry analysis of fluorescent-tuned epoxy-organosilica nanoparticles containing .

Flow cytometry analysis of fluorescent-tuned silica nanoparticles and multifluorescent silica nanoparticles. and nanoparticles without

Flow cytometry analysis of murine monocytes from whole blood. according to the protocol described herein.

Flow cytometry analysis of PMN from whoie biood of tumor bearing mice. according to the protocol described herein.

Flow cytometry analysis of silica particles surface-modified with protein and DNA. Epoxy-organosilica nanoparticles .

Flow cytometry analysis. CellQuest software. The fluorescence of 50,000 cells is measured.

Flow cytometry diagrams of HL-60 cells treated with a lac-PEG-SOD conjugate.

Flow cytometry of HeLa cells . Cells treated with the fluorinated constrnct NBD-F6-DPPE were 4.8-fold more intensely fluorescent than those incubated with the hydrocarbon analogue NBD-DPPE.

Flow DABCO Promotes the Conversion o R to S



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