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1 be isolated with the fluorescence-activated cell sorter.
2 ntibody NA1/34 and the fluorescent activated cell sorter.
3 rforin as detected by fluorescence-activated cell sorter.
4 C) isolated using the fluorescence-activated cell sorter.
5 tylglucosamine, and a fluorescence-activated cell sorter.
6 hi were isolated in a fluorescence-activated cell sorter.
7 infected cells with a fluorescence activated cell sorter.
8 n EPCs as assessed by 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 unohistochemistry and fluorescence activated cell sorter.
13 ony formation using a 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 lectronic microscopy, fluorescence-activated cell sorter analysis, and single-cell RNA sequencing.Mea
93 were characterized by fluorescent-activated cell sorter analysis, and TCR junctional region nucleoti
94 n epithelial cells in fluorescence-activated cell sorter analysis, as well as by coimmunoprecipitatio
96 ned and phenotyped by fluorescence-activated cell sorter analysis, in the peripheral blood mononuclea
97 es was performed with fluorescence-activated cell sorter analysis, inflammatory stimulation assays, a
98 n, as demonstrated by fluorescence-activated cell sorter analysis, suggesting that S(1190) maintains
99 cetuximab binding by fluorescence-activated cell sorter analysis, the number of DSBs by immunofluore
100 ive before surgery by fluorescence-activated cell sorter analysis, the PRA 3 days after implantation
101 se chain reaction and fluorescence-activated cell sorter analysis, we found that the ras transfectant
102 scence microscopy and fluorescence-activated cell sorter analysis, we localized and quantitated E- an
103 ages were measured by fluorescence-activated cell sorter analysis, whereas serum cytokines/chemokines
127 mented a fluorescence-activated microfluidic cell sorter and evaluated its performance on live, stabl
128 ified from naive mice via automated magnetic cell sorter and expanded ex vivo by anti-CD3/CD28 monocl
130 activation markers by fluorescence-activated cell sorter and induction of inflammatory cytokines usin
133 um were purified by a fluorescence-activated cell sorter and validated by cell-specific markers.
135 isoforms, purified by fluorescence-activated cell sorter, and analyzed in colony-forming assays and s
136 erism was followed by fluorescence-activated cell sorter, and graft survival was assessed by histolog
138 differential display, fluorescence-activated cell sorter, and overexpression analyses to assess the p
139 -cytometric analysis (fluorescence-activated cell sorter), apoptosis by DNA fragmentation (laddering)
140 ected HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic studies, in addition to
141 plication of a novel, fluorescence-activated cell sorter based assay that directly quantitates GC act
142 the development of a fluorescence-activated cell sorter-based assay for the quantitative analysis of
143 itive electroporation/fluorescence-activated cell sorter-based assay, we show that lysosomal exocytos
145 a novel nonselective fluorescence-activated cell sorter-based method and discovered that SB integrat
147 viruses, we devised a fluorescence-activated cell sorter-based screen to select virus-infected cells
148 type P. gingivalis by fluorescence-activated cell sorter, but not with noninvasive, fimbria-deficient
149 ous to a conventional fluorescence-activated cell sorter, but sorts droplets containing single cells
150 lume of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of o
151 on were determined by fluorescence-activated cell sorter (cell surface galectin-3), Western and North
152 dentify cell types by fluorescence-activated cell sorter.Conclusions: Lung and thyroid tissues were g
154 now commonplace with fluorescence activated cell sorters, development of comparable techniques that
155 We also established a fluorescence-activated cell sorter enrichment technique for major blood lineage
157 completion of TLI by fluorescence-activated cell sorter (FACS) analysis and enzyme-linked immunosorb
159 -CFC assay, as well as fluorescent activated cell sorter (FACS) analysis for Flk1(+) cells to determi
161 ession was detected by fluorescent-activated cell sorter (FACS) analysis in five of seven cases.
163 orescent as judged by fluorescence-activated cell sorter (FACS) analysis of infected cells in the abs
165 n was investigated by fluorescence-activated cell sorter (FACS) analysis of the DNA content in growth
166 ion was found between fluorescence-activated cell sorter (FACS) analysis results using annexin V to d
169 Using phosphoprotein fluorescence-activated cell sorter (FACS) analysis, atorvastatin treatment was
172 herein used combined fluorescence-activated cell sorter (FACS) and immunohistochemical (IHC) analyse
173 By using coupled fluorescence-activated cell sorter (FACS) and infection assays, we found that e
174 t assays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show th
175 34+ cells selected by fluorescence-activated cell sorter (FACS) from mobilized PBPC was 2 +/- 0.3-fol
176 ommercially available fluorescence-activated cell sorter (FACS) machines, making it possible to isola
182 minotransferase (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and i
183 uction was assayed by fluorescence-activated cell sorter (FACS), and the expanded T-cell cultures pro
184 n was assessed with a fluorescence-activated cell sorter (FACS), cell adhesion, and fluorescence micr
185 TNF-) were examined by fluorescent activated cell sorter (FACS), reduction of ferricytochrome C, and
188 ployed a differential fluorescence-activated cell sorter (FACS)-based sorting strategy using an Env t
189 ptase-PCR analysis of fluorescence-activated cell sorter (FACS)-purified CD4+ NK1.1+ T lymphocytes.
190 patients who received fluorescence activated cell sorter (FACS)-sorted autologous CD34+ hematopoietic
191 Contact coculture of fluorescence-activated cell sorter (FACS)-sorted bone marrow (BM) CD34(+)CD38-
192 ecipients of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)lin(-) cells were sacri
193 microarray studies on fluorescence-activated cell sorter (FACS)-sorted cells and microdissected GC ce
194 termined by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted peripheral blood from 20 serop
198 of subgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the activation of caspase 3
199 ells, fast enough to provide a decision to a cell sorter for real-time separation of individual targe
201 of ROSA26 tissues and fluorescence-activated cell sorter-Gal analysis of hematopoietic cells demonstr
203 tures were interrogated in the DEP-activated cell sorter in a continuous-flow manner, wherein the ele
204 culture assays or by fluorescence-activated cell sorter in the context of their therapeutic or diagn
205 eparation of cells by fluorescence-activated cell sorter indicate that there is a precise correlation
209 Using CD90.2 antibody and Magnetic Activated Cell Sorter (MACS) technique, we successfully purified T
210 CD34(+)-enriched cells were purified on the cell sorter (mean purity, 97.7% +/- 2.4%; n = 7), and ex
211 ped a Hi-D (11-color) fluorescence-activated cell sorter method in which we covalently couple a fluor
212 sable microfabricated fluorescence-activated cell sorter (microFACS) for sorting various biological e
214 ) were examined using fluorescence-activated cell sorter, mixed lymphocyte reaction, enzyme-linked im
216 e system, the multitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics
217 contrast, commercial fluorescence-activated cell sorters offer superior speed, sensitivity, and mult
218 rent populations by a fluorescence-activated cell sorter, placed in culture, and then reanalyzed by f
219 proteome analysis of fluorescence-activated cell sorter-purified beta-cells, tissue-comparative West
221 and annular channel geometry of the magnetic cell sorter require that a new strategy be developed for
223 method that uses the fluorescence-activated cell sorter selection of low Hoescht 33342/low Rhodamine
225 library, selecting by fluorescence-activated cell sorter single cells displaying low PAI promoter act
226 ht scatter and side-angle light scatter in a cell sorter, singly infected RBCs can be isolated and au
227 pplying this assay to fluorescence-activated cell sorter-sorted cell populations, we found that the L
228 y deregulated between fluorescence-activated cell sorter-sorted clonal B cells from the 3 disease gro
229 idization analysis of fluorescence-activated cell sorter-sorted CTCs also unraveled different cytogen
230 cells was analyzed by fluorescence-activated cell sorter staining, Western blotting with the monoclon
231 BCs bound anti-Gal by fluorescence-activated cell sorter, suggesting that these three GTs are alpha 1
232 examined in vitro by fluorescence-activated cell sorter, T-cell proliferation assays, enzyme-linked
233 Using quantitative fluorescence-activated cell sorter technology, we found that DC-SIGN is highly
235 s were assayed using a fluorescent-activated cell sorter to identify DiI-labeled reconstituted AMs, u
237 g of the malaria parasite; the method uses a cell sorter to rapidly isolate Plasmodium falciparum-inf
238 bsets, sorted using a fluorescence-activated cell sorter, to polarize IL-21(+)CXCL13(+) (IL-21-positi
240 amma) was analyzed by fluorescence-activated cell sorter, using one of the following antibodies: anti
241 nce, as quantified by fluorescence-activated cell sorter, varied inversely with disease progression.
242 e cell populations, a fluorescence-activated cell sorter was used to detect, sort, and enrich fibrobl
243 Coulter counter with a dc-dielectrophoretic cell sorter, we demonstrate simultaneous on-chip cell se