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1 unohistochemistry and fluorescence activated cell sorter.
2 ntibody NA1/34 and the fluorescent activated cell sorter.
3 rforin as detected by fluorescence-activated cell sorter.
4 n EPCs as assessed by fluorescence-activated cell sorter.
5 C) isolated using the fluorescence-activated cell sorter.
6 tylglucosamine, and a fluorescence-activated cell sorter.
7 hi were isolated in a fluorescence-activated cell sorter.
8 infected cells with a fluorescence activated cell sorter.
9 sts with the use of a fluorescence-activated cell sorter.
10 etylglucosamine, and a fluorescent activated cell sorter.
11 mice were examined by fluorescence-activated cell sorter.
12 ony formation using a fluorescence-activated cell sorter.
13 be isolated with the fluorescence-activated cell sorter.
14 lysis as in flow cytometric and microfluidic cell sorters.
15 eneration of cytometers, known as high-speed cell sorters.
16 ated from mutants in a fluorescent-activated cell sorter after labeling of K. lactis cells with fluor
17 eletal muscle using a fluorescence-activated cell sorter along with populations of regular myoblasts
18 and suspended in PBS, fluorescence-activated cell sorter analyses revealed the bacteria were only poo
23 e, as demonstrated by fluorescence-activated cell-sorter analyses (FACS), and perturbed receptor acti
25 gmentation assays and fluorescence-activated cell sorter analysis also indicated that ALK7 infection
28 ctive CD8+ T cells by fluorescence-activated cell sorter analysis and decreased production of the inf
31 te were determined by fluorescence-activated cell sorter analysis and immunofluorescence microscopy.
32 ochemical markers and fluorescence-activated cell sorter analysis and significantly increases mitotic
33 odamine 123 stain and fluorescence-activated cell sorter analysis and subjecting them to two apoptosi
34 despread as judged by fluorescence-activated cell sorter analysis and terminal deoxynucleotidyl trans
39 l exposure; and (iii) fluorescence-activated cell sorter analysis demonstrates significant intracellu
40 unosorbent assay, and fluorescence-activated cell sorter analysis employing a previously unreported m
41 Western blotting, and fluorescence-activated cell sorter analysis in CD45(+) pan-leukocytes isolated
42 C domain of Cripto by fluorescence-activated cell sorter analysis indicate that the CFC domain binds
45 microM), as shown by fluorescence-activated cell sorter analysis of cells stained with a fluorescent
51 microscopy and immuno-fluorescence-activated cell sorter analysis of isolated mitochondria show that
52 ne and [3H]thymidine, fluorescence-activated cell sorter analysis of murine leukemia virus-green fluo
53 kinetics, measured by fluorescence-activated cell sorter analysis of propidium iodide-stained cells,
54 8 hours of culture by fluorescence-activated cell sorter analysis of propidium iodidestained cells.
58 despite the fact that fluorescence-activated cell sorter analysis of these latter cells revealed that
64 tological appearance, fluorescence-activated cell sorter analysis revealed no significant difference
65 nfocal microscopy and fluorescence-activated cell sorter analysis revealed redistribution of endothel
66 Double labeling and fluorescence-activated cell sorter analysis revealed that ECs and 10T1/2 cells
79 d within 12-24 h, and fluorescence-activated cell sorter analysis suggests that treatment with these
84 sis, we phenotyped by fluorescence-activated cell sorter analysis various human tumor cell lines for
86 A) were measured, and fluorescence-activated cell sorter analysis was used to measure TNFRSF1A sheddi
87 PMNs as determined by fluorescence-activated cell sorter analysis with Annexin V and terminal deoxynu
89 ll surface antigen by fluorescence-activated cell sorter analysis with monoclonal antibodies reactive
90 otential (assessed by fluorescence-activated cell sorter analysis) from 15 to 30 minutes, which was p
92 were characterized by fluorescent-activated cell sorter analysis, and TCR junctional region nucleoti
93 n epithelial cells in fluorescence-activated cell sorter analysis, as well as by coimmunoprecipitatio
95 ned and phenotyped by fluorescence-activated cell sorter analysis, in the peripheral blood mononuclea
96 es was performed with fluorescence-activated cell sorter analysis, inflammatory stimulation assays, a
97 n, as demonstrated by fluorescence-activated cell sorter analysis, suggesting that S(1190) maintains
98 cetuximab binding by fluorescence-activated cell sorter analysis, the number of DSBs by immunofluore
99 ive before surgery by fluorescence-activated cell sorter analysis, the PRA 3 days after implantation
100 se chain reaction and fluorescence-activated cell sorter analysis, we found that the ras transfectant
101 scence microscopy and fluorescence-activated cell sorter analysis, we localized and quantitated E- an
102 ages were measured by fluorescence-activated cell sorter analysis, whereas serum cytokines/chemokines
126 mented a fluorescence-activated microfluidic cell sorter and evaluated its performance on live, stabl
127 ified from naive mice via automated magnetic cell sorter and expanded ex vivo by anti-CD3/CD28 monocl
129 activation markers by fluorescence-activated cell sorter and induction of inflammatory cytokines usin
131 um were purified by a fluorescence-activated cell sorter and validated by cell-specific markers.
133 isoforms, purified by fluorescence-activated cell sorter, and analyzed in colony-forming assays and s
134 erism was followed by fluorescence-activated cell sorter, and graft survival was assessed by histolog
136 differential display, fluorescence-activated cell sorter, and overexpression analyses to assess the p
137 -cytometric analysis (fluorescence-activated cell sorter), apoptosis by DNA fragmentation (laddering)
138 ected HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic studies, in addition to
139 plication of a novel, fluorescence-activated cell sorter based assay that directly quantitates GC act
140 the development of a fluorescence-activated cell sorter-based assay for the quantitative analysis of
141 itive electroporation/fluorescence-activated cell sorter-based assay, we show that lysosomal exocytos
142 a novel nonselective fluorescence-activated cell sorter-based method and discovered that SB integrat
144 viruses, we devised a fluorescence-activated cell sorter-based screen to select virus-infected cells
145 type P. gingivalis by fluorescence-activated cell sorter, but not with noninvasive, fimbria-deficient
146 lume of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of o
147 on were determined by fluorescence-activated cell sorter (cell surface galectin-3), Western and North
149 now commonplace with fluorescence activated cell sorters, development of comparable techniques that
150 We also established a fluorescence-activated cell sorter enrichment technique for major blood lineage
152 completion of TLI by fluorescence-activated cell sorter (FACS) analysis and enzyme-linked immunosorb
154 -CFC assay, as well as fluorescent activated cell sorter (FACS) analysis for Flk1(+) cells to determi
156 ession was detected by fluorescent-activated cell sorter (FACS) analysis in five of seven cases.
158 orescent as judged by fluorescence-activated cell sorter (FACS) analysis of infected cells in the abs
160 n was investigated by fluorescence-activated cell sorter (FACS) analysis of the DNA content in growth
161 ion was found between fluorescence-activated cell sorter (FACS) analysis results using annexin V to d
164 Using phosphoprotein fluorescence-activated cell sorter (FACS) analysis, atorvastatin treatment was
167 herein used combined fluorescence-activated cell sorter (FACS) and immunohistochemical (IHC) analyse
168 By using coupled fluorescence-activated cell sorter (FACS) and infection assays, we found that e
169 t assays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show th
170 34+ cells selected by fluorescence-activated cell sorter (FACS) from mobilized PBPC was 2 +/- 0.3-fol
176 minotransferase (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and i
177 uction was assayed by fluorescence-activated cell sorter (FACS), and the expanded T-cell cultures pro
178 TNF-) were examined by fluorescent activated cell sorter (FACS), reduction of ferricytochrome C, and
181 ployed a differential fluorescence-activated cell sorter (FACS)-based sorting strategy using an Env t
182 ptase-PCR analysis of fluorescence-activated cell sorter (FACS)-purified CD4+ NK1.1+ T lymphocytes.
183 patients who received fluorescence activated cell sorter (FACS)-sorted autologous CD34+ hematopoietic
184 Contact coculture of fluorescence-activated cell sorter (FACS)-sorted bone marrow (BM) CD34(+)CD38-
185 ecipients of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)lin(-) cells were sacri
186 microarray studies on fluorescence-activated cell sorter (FACS)-sorted cells and microdissected GC ce
187 termined by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted peripheral blood from 20 serop
191 of subgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the activation of caspase 3
193 of ROSA26 tissues and fluorescence-activated cell sorter-Gal analysis of hematopoietic cells demonstr
195 tures were interrogated in the DEP-activated cell sorter in a continuous-flow manner, wherein the ele
196 culture assays or by fluorescence-activated cell sorter in the context of their therapeutic or diagn
197 eparation of cells by fluorescence-activated cell sorter indicate that there is a precise correlation
201 CD34(+)-enriched cells were purified on the cell sorter (mean purity, 97.7% +/- 2.4%; n = 7), and ex
202 ped a Hi-D (11-color) fluorescence-activated cell sorter method in which we covalently couple a fluor
203 sable microfabricated fluorescence-activated cell sorter (microFACS) for sorting various biological e
205 ) were examined using fluorescence-activated cell sorter, mixed lymphocyte reaction, enzyme-linked im
207 e system, the multitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics
208 rent populations by a fluorescence-activated cell sorter, placed in culture, and then reanalyzed by f
209 proteome analysis of fluorescence-activated cell sorter-purified beta-cells, tissue-comparative West
211 and annular channel geometry of the magnetic cell sorter require that a new strategy be developed for
213 method that uses the fluorescence-activated cell sorter selection of low Hoescht 33342/low Rhodamine
215 library, selecting by fluorescence-activated cell sorter single cells displaying low PAI promoter act
216 ht scatter and side-angle light scatter in a cell sorter, singly infected RBCs can be isolated and au
217 pplying this assay to fluorescence-activated cell sorter-sorted cell populations, we found that the L
218 y deregulated between fluorescence-activated cell sorter-sorted clonal B cells from the 3 disease gro
219 idization analysis of fluorescence-activated cell sorter-sorted CTCs also unraveled different cytogen
220 cells was analyzed by fluorescence-activated cell sorter staining, Western blotting with the monoclon
221 BCs bound anti-Gal by fluorescence-activated cell sorter, suggesting that these three GTs are alpha 1
222 examined in vitro by fluorescence-activated cell sorter, T-cell proliferation assays, enzyme-linked
223 Using quantitative fluorescence-activated cell sorter technology, we found that DC-SIGN is highly
225 s were assayed using a fluorescent-activated cell sorter to identify DiI-labeled reconstituted AMs, u
227 g of the malaria parasite; the method uses a cell sorter to rapidly isolate Plasmodium falciparum-inf
229 amma) was analyzed by fluorescence-activated cell sorter, using one of the following antibodies: anti
230 nce, as quantified by fluorescence-activated cell sorter, varied inversely with disease progression.
231 e cell populations, a fluorescence-activated cell sorter was used to detect, sort, and enrich fibrobl
232 Coulter counter with a dc-dielectrophoretic cell sorter, we demonstrate simultaneous on-chip cell se
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