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1 ormation using a fluorescence-activated cell sorter.
2 solated with the fluorescence-activated cell sorter.
3 dy NA1/34 and the fluorescent activated cell sorter.
4 n as detected by fluorescence-activated cell sorter.
5 olated using the fluorescence-activated cell sorter.
6 ucosamine, and a fluorescence-activated cell sorter.
7 re isolated in a fluorescence-activated cell sorter.
8 ted cells with a fluorescence activated cell sorter.
9 ith the use of a fluorescence-activated cell sorter.
10 s as assessed by fluorescence-activated cell sorter.
11 lucosamine, and a fluorescent activated cell sorter.
12 stochemistry and fluorescence activated cell sorter.
13 were examined by fluorescence-activated cell sorter.
14 tion of cytometers, known as high-speed cell sorters.
15 esign of dielectrophoretic concentrators and sorters.
16 as in flow cytometric and microfluidic cell sorters.
17 olve N-glycans as sorting signals, or lectin sorters.
19 nt microfluidic absorbance-activated droplet sorter (AADS) that extends the range of assays amenable
20 from mutants in a fluorescent-activated cell sorter after labeling of K. lactis cells with fluorescei
22 l muscle using a fluorescence-activated cell sorter along with populations of regular myoblasts and e
23 abled systematic assessment of multiple flow sorters, alongside their operational parameters using th
24 of derivative chromosomes using a MoFlo flow sorter, amplification of these derivatives using whole-g
25 demonstrated by fluorescence-activated cell-sorter analyses (FACS), and perturbed receptor activatio
26 uspended in PBS, fluorescence-activated cell sorter analyses revealed the bacteria were only poorly f
28 In addition, fluorescence-activated cell sorter analyses with a specific rabbit anti-Lmsp1 antise
32 ation assays and fluorescence-activated cell sorter analysis also indicated that ALK7 infection induc
35 CD8+ T cells by fluorescence-activated cell sorter analysis and decreased production of the inflamma
39 ical markers and fluorescence-activated cell sorter analysis and significantly increases mitotic cell
40 ne 123 stain and fluorescence-activated cell sorter analysis and subjecting them to two apoptosis ind
41 ead as judged by fluorescence-activated cell sorter analysis and terminal deoxynucleotidyl transferas
48 osure; and (iii) fluorescence-activated cell sorter analysis demonstrates significant intracellular o
49 rbent assay, and fluorescence-activated cell sorter analysis employing a previously unreported method
50 rn blotting, and fluorescence-activated cell sorter analysis in CD45(+) pan-leukocytes isolated from
51 ain of Cripto by fluorescence-activated cell sorter analysis indicate that the CFC domain binds to AL
54 oM), as shown by fluorescence-activated cell sorter analysis of cells stained with a fluorescent Delt
58 In addition, fluorescence-activated cell sorter analysis of FTI-treated KNRK cells shows a sub-G1
60 scopy and immuno-fluorescence-activated cell sorter analysis of isolated mitochondria show that the m
61 d [3H]thymidine, fluorescence-activated cell sorter analysis of murine leukemia virus-green fluoresce
63 ics, measured by fluorescence-activated cell sorter analysis of propidium iodide-stained cells, indic
68 te the fact that fluorescence-activated cell sorter analysis of these latter cells revealed that the
72 Furthermore, fluorescence-activated cell sorter analysis on spleen cells showed that IL-12 neutra
74 ical appearance, fluorescence-activated cell sorter analysis revealed no significant difference in to
75 l microscopy and fluorescence-activated cell sorter analysis revealed redistribution of endothelial g
76 ble labeling and fluorescence-activated cell sorter analysis revealed that ECs and 10T1/2 cells were
82 Furthermore, fluorescence-activated cell sorter analysis reveals that those alleles that cause el
89 hin 12-24 h, and fluorescence-activated cell sorter analysis suggests that treatment with these compo
94 we phenotyped by fluorescence-activated cell sorter analysis various human tumor cell lines for expre
96 re measured, and fluorescence-activated cell sorter analysis was used to measure TNFRSF1A shedding fr
97 as determined by fluorescence-activated cell sorter analysis with Annexin V and terminal deoxynucleot
99 rface antigen by fluorescence-activated cell sorter analysis with monoclonal antibodies reactive with
100 ial (assessed by fluorescence-activated cell sorter analysis) from 15 to 30 minutes, which was partia
102 characterized by fluorescent-activated cell sorter analysis, and TCR junctional region nucleotide se
103 thelial cells in fluorescence-activated cell sorter analysis, as well as by coimmunoprecipitation.
105 nd phenotyped by fluorescence-activated cell sorter analysis, in the peripheral blood mononuclear cel
106 s performed with fluorescence-activated cell sorter analysis, inflammatory stimulation assays, and tr
107 demonstrated by fluorescence-activated cell sorter analysis, suggesting that S(1190) maintains the b
108 ximab binding by fluorescence-activated cell sorter analysis, the number of DSBs by immunofluorescenc
109 efore surgery by fluorescence-activated cell sorter analysis, the PRA 3 days after implantation of th
110 ain reaction and fluorescence-activated cell sorter analysis, we found that the ras transfectants exp
111 e microscopy and fluorescence-activated cell sorter analysis, we localized and quantitated E- and P-c
112 were measured by fluorescence-activated cell sorter analysis, whereas serum cytokines/chemokines were
134 d a fluorescence-activated microfluidic cell sorter and evaluated its performance on live, stably tra
135 from naive mice via automated magnetic cell sorter and expanded ex vivo by anti-CD3/CD28 monoclonal
137 ation markers by fluorescence-activated cell sorter and induction of inflammatory cytokines using an
139 : the Genome Browser, Proteome Browser, Gene Sorter and Table Browser offered at the UCSC website.
142 apable of higher throughput than traditional sorters and can distinguish subtler differences between
143 rms, purified by fluorescence-activated cell sorter, and analyzed in colony-forming assays and suspen
144 was followed by fluorescence-activated cell sorter, and graft survival was assessed by histology.
146 rential display, fluorescence-activated cell sorter, and overexpression analyses to assess the potent
147 metric analysis (fluorescence-activated cell sorter), apoptosis by DNA fragmentation (laddering), flo
148 hotons in a nonlinear crystal and use a mode sorter as the quantum interface to transfer the entangle
149 progress in miniaturized flow-based optical sorters as well as in sorting following static microscop
150 HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic studies, in addition to funct
151 tion of a novel, fluorescence-activated cell sorter based assay that directly quantitates GC activity
152 development of a fluorescence-activated cell sorter-based assay for the quantitative analysis of beta
153 electroporation/fluorescence-activated cell sorter-based assay, we show that lysosomal exocytosis tr
154 vel nonselective fluorescence-activated cell sorter-based method and discovered that SB integrates ap
155 Here we use fluorescence-activated cell sorter-based protocols to test distinct hematopoietic fr
156 es, we devised a fluorescence-activated cell sorter-based screen to select virus-infected cells that
157 P. gingivalis by fluorescence-activated cell sorter, but not with noninvasive, fimbria-deficient muta
158 magnetic dipole, thus establishing that our sorter can be an instrument for nanoscale magnetic spect
159 of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of optica
161 re determined by fluorescence-activated cell sorter (cell surface galectin-3), Western and Northern a
162 uated Complex Object Parametric Analyzer and Sorter (COPAS) large particle flow cytometry for the det
163 chnology is a fluorescence-activated droplet sorter coupled to a specialized substrate that together
165 commonplace with fluorescence activated cell sorters, development of comparable techniques that nonde
166 we have adapted a microfluidic constriction sorter device to separate a wide range of nucleic acid a
168 r, the Known Genes details page and the Gene Sorter; domain information from Superfamily, InterPro an
170 d using a Grating orienting task and a Shape-sorter-drum task, and with somatosensory-evoked magnetic
171 so established a fluorescence-activated cell sorter enrichment technique for major blood lineages and
172 compact directional light-filters and colour-sorters exhibiting angle- or spectrally-tunable optical
174 letion of TLI by fluorescence-activated cell sorter (FACS) analysis and enzyme-linked immunosorbent a
176 assay, as well as fluorescent activated cell sorter (FACS) analysis for Flk1(+) cells to determine qu
180 ent as judged by fluorescence-activated cell sorter (FACS) analysis of infected cells in the absence
182 investigated by fluorescence-activated cell sorter (FACS) analysis of the DNA content in growth-arre
183 as found between fluorescence-activated cell sorter (FACS) analysis results using annexin V to detect
186 g phosphoprotein fluorescence-activated cell sorter (FACS) analysis, atorvastatin treatment was found
190 in used combined fluorescence-activated cell sorter (FACS) and immunohistochemical (IHC) analyses of
191 By using coupled fluorescence-activated cell sorter (FACS) and infection assays, we found that even v
192 ays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show that ex
193 ells selected by fluorescence-activated cell sorter (FACS) from mobilized PBPC was 2 +/- 0.3-fold and
194 ubgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the activation of caspase 3, and
200 ransferase (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and inflam
201 n was assayed by fluorescence-activated cell sorter (FACS), and the expanded T-cell cultures produced
202 were examined by fluorescent activated cell sorter (FACS), reduction of ferricytochrome C, and bioas
204 Here we use a fluorescence-activated cell sorter (FACS)-based approach to investigate expression o
205 d a differential fluorescence-activated cell sorter (FACS)-based sorting strategy using an Env trimer
207 nts who received fluorescence activated cell sorter (FACS)-sorted autologous CD34+ hematopoietic prog
208 act coculture of fluorescence-activated cell sorter (FACS)-sorted bone marrow (BM) CD34(+)CD38- cells
209 ents of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)lin(-) cells were sacrificed
210 array studies on fluorescence-activated cell sorter (FACS)-sorted cells and microdissected GC cells.
211 ned by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted peripheral blood from 20 seropositi
217 SA26 tissues and fluorescence-activated cell sorter-Gal analysis of hematopoietic cells demonstrates
218 versity of California Santa Cruz (UCSC) Gene Sorter has been created as a gene-based counterpart to t
220 were interrogated in the DEP-activated cell sorter in a continuous-flow manner, wherein the electric
221 ure assays or by fluorescence-activated cell sorter in the context of their therapeutic or diagnostic
222 tion of cells by fluorescence-activated cell sorter indicate that there is a precise correlation betw
226 (+)-enriched cells were purified on the cell sorter (mean purity, 97.7% +/- 2.4%; n = 7), and examine
227 Hi-D (11-color) fluorescence-activated cell sorter method in which we covalently couple a fluorescen
228 microfabricated fluorescence-activated cell sorter (microFACS) for sorting various biological entiti
230 e examined using fluorescence-activated cell sorter, mixed lymphocyte reaction, enzyme-linked immunos
232 tem, the multitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics techn
233 populations by a fluorescence-activated cell sorter, placed in culture, and then reanalyzed by flow c
234 eome analysis of fluorescence-activated cell sorter-purified beta-cells, tissue-comparative Western b
237 nnular channel geometry of the magnetic cell sorter require that a new strategy be developed for opti
239 od that uses the fluorescence-activated cell sorter selection of low Hoescht 33342/low Rhodamine 123
240 The data reveal that dielectrophoretic cell sorters should have the ability to discriminate between,
241 ry, selecting by fluorescence-activated cell sorter single cells displaying low PAI promoter activity
242 atter and side-angle light scatter in a cell sorter, singly infected RBCs can be isolated and automat
243 ng this assay to fluorescence-activated cell sorter-sorted cell populations, we found that the Lin(-)
244 egulated between fluorescence-activated cell sorter-sorted clonal B cells from the 3 disease groups.
245 tion analysis of fluorescence-activated cell sorter-sorted CTCs also unraveled different cytogenetic
246 was analyzed by fluorescence-activated cell sorter staining, Western blotting with the monoclonal an
247 ound anti-Gal by fluorescence-activated cell sorter, suggesting that these three GTs are alpha 1,3 GT
248 ined in vitro by fluorescence-activated cell sorter, T-cell proliferation assays, enzyme-linked immun
250 ing quantitative fluorescence-activated cell sorter technology, we found that DC-SIGN is highly expre
251 We demonstrate a high-speed microfluidic sorter that can isolate and immobilize Caenorhabditis el
252 in a two-stage, continuous-flow microfluidic sorter that separates antibody-binding target cells capt
254 including BLAT, the Table Browser, the Gene Sorter, the Proteome Browser, VisiGene and Genome Graphs
255 Appropriate gates are constructed on a cell sorter to exclude dead cells and lineage (CD45(+)Ter-119
256 e assayed using a fluorescent-activated cell sorter to identify DiI-labeled reconstituted AMs, unlabe
259 the malaria parasite; the method uses a cell sorter to rapidly isolate Plasmodium falciparum-infected
260 responsive enhanced GFP reporter, and a flow sorter to recover dominant modulators of reporter expres
262 was analyzed by fluorescence-activated cell sorter, using one of the following antibodies: anti-OX3,
264 l populations, a fluorescence-activated cell sorter was used to detect, sort, and enrich fibroblast p
265 ter counter with a dc-dielectrophoretic cell sorter, we demonstrate simultaneous on-chip cell separat
267 r, using a device referred to as an OAM mode sorter, we show that OAM modes can be (de)multiplexed ov
268 ial microfluidic (trapezoidal cross-section) sorter with enhanced separation resolution and demonstra
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