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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 stochemistry and fluorescence activated cell sorter.
5 n as detected by fluorescence-activated cell sorter.
6 olated using the fluorescence-activated cell sorter.
7 ucosamine, and a fluorescence-activated cell sorter.
8 re isolated in a fluorescence-activated cell sorter.
9 ted cells with a fluorescence activated cell sorter.
10 ith the use of a fluorescence-activated cell sorter.
11 lucosamine, and a fluorescent activated cell sorter.
12 iously developed deformability-based droplet sorter.
13 s as assessed by fluorescence-activated cell sorter.
14 were examined by fluorescence-activated cell sorter.
15 tion of cytometers, known as high-speed cell sorters.
16 esign of dielectrophoretic concentrators and sorters.
17 olve N-glycans as sorting signals, or lectin sorters.
18 y optical transformations and universal mode sorters.
19 re comprehensively benchmark automated spike sorters.
20  as in flow cytometric and microfluidic cell sorters.
21 eneration Opto-Volume-based Accurate droplet sorter), a device capable of discerning droplets based o
22                                     The Gene Sorter, a CGI-based Web application written in C with a
23 nt microfluidic absorbance-activated droplet sorter (AADS) that extends the range of assays amenable
24 from mutants in a fluorescent-activated cell sorter after labeling of K. lactis cells with fluorescei
25  The implementation of CoMIT and its Variant Sorter Algorithm are described.
26 or Inclusivity Tool (CoMIT) uses the Variant Sorter Algorithm to sidestep multiple sequence alignment
27                                     The Gene Sorter allows filtering and comparison of genes by sever
28 l muscle using a fluorescence-activated cell sorter along with populations of regular myoblasts and e
29 abled systematic assessment of multiple flow sorters, alongside their operational parameters using th
30 d from separate channels of the constriction sorter amounted to >90% and were in excellent agreement
31 of derivative chromosomes using a MoFlo flow sorter, amplification of these derivatives using whole-g
32  demonstrated by fluorescence-activated cell-sorter analyses (FACS), and perturbed receptor activatio
33 uspended in PBS, fluorescence-activated cell sorter analyses revealed the bacteria were only poorly f
34 t microscopy and fluorescence-activated cell sorter analyses were used, respectively.
35     In addition, fluorescence-activated cell sorter analyses with a specific rabbit anti-Lmsp1 antise
36  demonstrated by fluorescence-activated cell sorter analyses.
37 ermined by using fluorescence-activated cell sorter analyses.
38                  Fluorescence-activated cell sorter analysis (flow cytometric analysis) of peripheral
39 ation assays and fluorescence-activated cell sorter analysis also indicated that ALK7 infection induc
40 n as detected by fluorescence-activated cell sorter analysis and confocal microscopy.
41 ng Western blot, fluorescence-activated cell sorter analysis and confocal microscopy.
42  CD8+ T cells by fluorescence-activated cell sorter analysis and decreased production of the inflamma
43                  Fluorescence activated cell sorter analysis and histological examination of serial l
44 characterized by fluorescence-activated cell sorter analysis and immunocytochemistry.
45 re determined by fluorescence-activated cell sorter analysis and immunofluorescence microscopy.
46 ical markers and fluorescence-activated cell sorter analysis and significantly increases mitotic cell
47 ne 123 stain and fluorescence-activated cell sorter analysis and subjecting them to two apoptosis ind
48 ead as judged by fluorescence-activated cell sorter analysis and terminal deoxynucleotidyl transferas
49 t 33342 staining/fluorescence-activated cell-sorter analysis before injection.
50                  Fluorescence-activated cell sorter analysis confirmed that the 7mG cap structure was
51                   Fluorescent-activated cell sorter analysis demonstrated that dexamethasone induced
52                              Flow cytometric sorter analysis demonstrated that regulatory-associated
53                  Fluorescence-activated cell sorter analysis demonstrated that the arrest of the cell
54                  Fluorescence-activated cell sorter analysis demonstrated that the S-phase cells did
55 osure; and (iii) fluorescence-activated cell sorter analysis demonstrates significant intracellular o
56 rbent assay, and fluorescence-activated cell sorter analysis employing a previously unreported method
57 rn blotting, and fluorescence-activated cell sorter analysis in CD45(+) pan-leukocytes isolated from
58 ain of Cripto by fluorescence-activated cell sorter analysis indicate that the CFC domain binds to AL
59                  Fluorescence-activated cell sorter analysis indicated that sangivamycin induced cell
60                                         Cell sorter analysis of CD11b+ bone marrow cells revealed sim
61 oM), as shown by fluorescence-activated cell sorter analysis of cells stained with a fluorescent Delt
62                  Fluorescence-activated cell sorter analysis of cultures after 21 days showed a signi
63                  Fluorescence-activated cell sorter analysis of enriched stem cell populations showed
64                  Fluorescence-activated cell sorter analysis of freshly isolated peripheral blood mon
65     In addition, fluorescence-activated cell sorter analysis of FTI-treated KNRK cells shows a sub-G1
66                  Fluorescence-activated cell sorter analysis of hCD152-hCD59 transduced primary porci
67 scopy and immuno-fluorescence-activated cell sorter analysis of isolated mitochondria show that the m
68 d [3H]thymidine, fluorescence-activated cell sorter analysis of murine leukemia virus-green fluoresce
69 e-mutant mice on fluorescence-activated cell-sorter analysis of peripheral neutrophils.
70 ics, measured by fluorescence-activated cell sorter analysis of propidium iodide-stained cells, indic
71 rs of culture by fluorescence-activated cell sorter analysis of propidium iodidestained cells.
72 tion assays, and fluorescence-activated cell sorter analysis of propidium-labeled nuclei.
73                  Fluorescence-activated cell sorter analysis of prostatic tissue from 11-18-month-old
74          However, fluoroscein-activated cell sorter analysis of retinal leukocytic infiltrate indicat
75 te the fact that fluorescence-activated cell sorter analysis of these latter cells revealed that the
76                  Fluorescence-activated cell sorter analysis of tumor tissue revealed depletion of pe
77                  Fluorescence-activated cell sorter analysis of Vbeta expression in alloreactive CD4+
78                  Fluorescence-activated cell sorter analysis on EGFP(+) fetal blood cells revealed th
79     Furthermore, fluorescence-activated cell sorter analysis on spleen cells showed that IL-12 neutra
80                  Fluorescence-activated cell sorter analysis revealed less leukocyte infiltration in
81 ical appearance, fluorescence-activated cell sorter analysis revealed no significant difference in to
82 l microscopy and fluorescence-activated cell sorter analysis revealed redistribution of endothelial g
83 ble labeling and fluorescence-activated cell sorter analysis revealed that ECs and 10T1/2 cells were
84                  Fluorescence-activated cell sorter analysis revealed that ISIS 14435/14439-induced g
85                   Fluorescent-activated cell sorter analysis revealed that PB-CD31(+) cells exhibited
86                  Fluorescence-activated cell sorter analysis revealed that PBD155 treatment affected
87                  Fluorescence-activated cell sorter analysis revealed that this low level of DNA synt
88                  Fluorescence-activated cell sorter analysis revealed that, although uninfected IL-2(
89     Furthermore, fluorescence-activated cell sorter analysis reveals that those alleles that cause el
90        Moreover, fluorescence-activated cell sorter analysis showed that 25 to 90% of the T cells wer
91                  Fluorescence-activated cell sorter analysis showed that RAP significantly enhances t
92                  Fluorescence-activated cell sorter analysis showed that the antigen-responsive lines
93                  Fluorescence-activated cell sorter analysis showed treatment with cOX6 significantly
94                  Fluorescence-activated cell sorter analysis shows that IL-17B and IL-17C bind to THP
95                  Fluorescence-activated cell sorter analysis suggested that PC3 cells expressing MBP-
96 hin 12-24 h, and fluorescence-activated cell sorter analysis suggests that treatment with these compo
97      We found by fluorescence-activated cell sorter analysis that serotype AD strains are aneuploid o
98       We coupled fluorescence-activated cell sorter analysis using anti-CD45 monoclonal antibody with
99                  Fluorescence-activated cell sorter analysis using soluble tetrameric major histocomp
100                  Fluorescence-activated cell sorter analysis using the anti-gp60 antibodies demonstra
101 we phenotyped by fluorescence-activated cell sorter analysis various human tumor cell lines for expre
102                  Fluorescence-activated cell sorter analysis was performed on whole human blood (n=2)
103 re measured, and fluorescence-activated cell sorter analysis was used to measure TNFRSF1A shedding fr
104 as determined by fluorescence-activated cell sorter analysis with Annexin V and terminal deoxynucleot
105                  Fluorescence-activated cell sorter analysis with Ebp-specific antibodies confirmed t
106 rface antigen by fluorescence-activated cell sorter analysis with monoclonal antibodies reactive with
107 ial (assessed by fluorescence-activated cell sorter analysis) from 15 to 30 minutes, which was partia
108 t nor apoptosis (fluorescence-activated cell sorter analysis).
109 onic microscopy, fluorescence-activated cell sorter analysis, and single-cell RNA sequencing.Measurem
110  characterized by fluorescent-activated cell sorter analysis, and TCR junctional region nucleotide se
111 thelial cells in fluorescence-activated cell sorter analysis, as well as by coimmunoprecipitation.
112                  Fluorescence-activated cell sorter analysis, continuous labeling with tritiated thym
113 nd phenotyped by fluorescence-activated cell sorter analysis, in the peripheral blood mononuclear cel
114 s performed with fluorescence-activated cell sorter analysis, inflammatory stimulation assays, and tr
115  demonstrated by fluorescence-activated cell sorter analysis, suggesting that S(1190) maintains the b
116 ximab binding by fluorescence-activated cell sorter analysis, the number of DSBs by immunofluorescenc
117 efore surgery by fluorescence-activated cell sorter analysis, the PRA 3 days after implantation of th
118 ain reaction and fluorescence-activated cell sorter analysis, we found that the ras transfectants exp
119 e microscopy and fluorescence-activated cell sorter analysis, we localized and quantitated E- and P-c
120 were measured by fluorescence-activated cell sorter analysis, whereas serum cytokines/chemokines were
121 orbent assay and fluorescence-activated cell sorter analysis.
122 ssay followed by fluorescence-activated cell sorter analysis.
123  was measured by fluorescence-activated cell sorter analysis.
124 also examined by fluorescence activated cell sorter analysis.
125 ain reaction and fluorescence-activated cell sorter analysis.
126 as determined by fluorescence-activated cell sorter analysis.
127  was assessed by fluorescence-activated cell sorter analysis.
128  was assessed by fluorescence-activated cell sorter analysis.
129 as determined by fluorescence-activated cell sorter analysis.
130 ine coupled with fluorescence-activated cell sorter analysis.
131 istochemistry and fluorescent-activated-cell-sorter analysis.
132 ue exclusion and fluorescence-activated cell sorter analysis.
133 ) as assessed by fluorescence-activated cell sorter analysis.
134 CCR5-positive by fluorescence-activated cell sorter analysis.
135 cells by 2-color fluorescence-activated cell sorter analysis.
136 ility complex by fluorescence-activated cell sorter analysis.
137 corporation, and fluorescence-activated cell sorter analysis.
138 tion followed by fluorescence-activated cell sorter analysis.
139  was assessed by fluorescence-activated cell sorter analysis.
140                  Fluorescence-activated cell sorter and confocal microscopy revealed that knockdown o
141 nker and used in fluorescence-activated cell sorter and ELISA analyses.
142 d a fluorescence-activated microfluidic cell sorter and evaluated its performance on live, stably tra
143  from naive mice via automated magnetic cell sorter and expanded ex vivo by anti-CD3/CD28 monoclonal
144                  Fluorescence-activated cell sorter and immunofluorescent analysis were used to detec
145 ation markers by fluorescence-activated cell sorter and induction of inflammatory cytokines using an
146 ides neuroscientists to an optimal choice of sorter and parameters for a wide range of probes and bra
147  was assessed by fluorescence-activated cell sorter and polymerase chain reaction (PCR).
148 selected using a fluorescence-activated cell sorter and regrown.
149 : the Genome Browser, Proteome Browser, Gene Sorter and Table Browser offered at the UCSC website.
150 re purified by a fluorescence-activated cell sorter and validated by cell-specific markers.
151       We show by fluorescence-activated cell sorter and/or confocal microscopy analysis that an enhan
152 apable of higher throughput than traditional sorters and can distinguish subtler differences between
153 rms, purified by fluorescence-activated cell sorter, and analyzed in colony-forming assays and suspen
154 led droplets are sorted using a microfluidic sorter, and genomes are extracted for sequencing.
155  was followed by fluorescence-activated cell sorter, and graft survival was assessed by histology.
156  isolated with a fluorescence-activated cell sorter, and inserts were partially sequenced.
157 rential display, fluorescence-activated cell sorter, and overexpression analyses to assess the potent
158 metric analysis (fluorescence-activated cell sorter), apoptosis by DNA fragmentation (laddering), flo
159 hotons in a nonlinear crystal and use a mode sorter as the quantum interface to transfer the entangle
160  progress in miniaturized flow-based optical sorters as well as in sorting following static microscop
161  HeLa cells, and fluorescence-activated cell sorter-assisted phenotypic studies, in addition to funct
162 tion of a novel, fluorescence-activated cell sorter based assay that directly quantitates GC activity
163 development of a fluorescence-activated cell sorter-based assay for the quantitative analysis of beta
164  electroporation/fluorescence-activated cell sorter-based assay, we show that lysosomal exocytosis tr
165  High-throughput fluorescence-activated cell sorter-based bead screening was used to select molecules
166 vel nonselective fluorescence-activated cell sorter-based method and discovered that SB integrates ap
167      Here we use fluorescence-activated cell sorter-based protocols to test distinct hematopoietic fr
168 es, we devised a fluorescence-activated cell sorter-based screen to select virus-infected cells that
169 P. gingivalis by fluorescence-activated cell sorter, but not with noninvasive, fimbria-deficient muta
170 o a conventional fluorescence-activated cell sorter, but sorts droplets containing single cells withi
171  magnetic dipole, thus establishing that our sorter can be an instrument for nanoscale magnetic spect
172 of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of optica
173                                        These sorters can function as stand-alone devices or as compon
174 re determined by fluorescence-activated cell sorter (cell surface galectin-3), Western and Northern a
175 fy cell types by fluorescence-activated cell sorter.Conclusions: Lung and thyroid tissues were genera
176 uated Complex Object Parametric Analyzer and Sorter (COPAS) large particle flow cytometry for the det
177 chnology is a fluorescence-activated droplet sorter coupled to a specialized substrate that together
178  was negative by fluorescence-activated cell sorter cross-match on day 64.
179 commonplace with fluorescence activated cell sorters, development of comparable techniques that nonde
180 sing an iDEP-based microfluidic constriction sorter device for length-based sorting.
181  we have adapted a microfluidic constriction sorter device to separate a wide range of nucleic acid a
182 obeads and an inertial microfluidic particle sorter device.
183 r, the Known Genes details page and the Gene Sorter; domain information from Superfamily, InterPro an
184 nstrating the feasibility of using molecular sorters driven by motor proteins.
185 d using a Grating orienting task and a Shape-sorter-drum task, and with somatosensory-evoked magnetic
186 so established a fluorescence-activated cell sorter enrichment technique for major blood lineages and
187 compact directional light-filters and colour-sorters exhibiting angle- or spectrally-tunable optical
188                  Fluorescence-activated cell sorter (FACS) analyses revealed significantly lower numb
189 letion of TLI by fluorescence-activated cell sorter (FACS) analysis and enzyme-linked immunosorbent a
190                  Fluorescence-activated cell sorter (FACS) analysis demonstrated a significant increa
191 assay, as well as fluorescent activated cell sorter (FACS) analysis for Flk1(+) cells to determine qu
192                  Fluorescence-activated cell sorter (FACS) analysis identified a high frequency of VE
193 n was detected by fluorescent-activated cell sorter (FACS) analysis in five of seven cases.
194                  Fluorescence-activated cell sorter (FACS) analysis of cell permeability showed the e
195 ent as judged by fluorescence-activated cell sorter (FACS) analysis of infected cells in the absence
196                  Fluorescence-activated cell sorter (FACS) analysis of the composition of lung leukoc
197  investigated by fluorescence-activated cell sorter (FACS) analysis of the DNA content in growth-arre
198 as found between fluorescence-activated cell sorter (FACS) analysis results using annexin V to detect
199                   Fluorescent-activated cell sorter (FACS) analysis was used to study the effects of
200                  Fluorescence-activated cell sorter (FACS) analysis with some, but not all, mouse ant
201 g phosphoprotein fluorescence-activated cell sorter (FACS) analysis, atorvastatin treatment was found
202  was measured by fluorescence-activated cell sorter (FACS) analysis.
203 tes (PMNs) using fluorescence-activated cell-sorter (FACS) analysis.
204 e microscopy and fluorescence-activated cell sorter (FACS) analysis.
205 in used combined fluorescence-activated cell sorter (FACS) and immunohistochemical (IHC) analyses of
206 By using coupled fluorescence-activated cell sorter (FACS) and infection assays, we found that even v
207 ays (ELISAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show that ex
208 ells selected by fluorescence-activated cell sorter (FACS) from mobilized PBPC was 2 +/- 0.3-fold and
209 cially available fluorescence-activated cell sorter (FACS) machines, making it possible to isolate si
210 ubgenomic DNA in fluorescence-activated cell-sorter (FACS) profiles, the activation of caspase 3, and
211                  Flourescence-activated cell sorter (FACS) purified CD56+/CD3- NK cells cultured alon
212       Culture of fluorescence-activated cell sorter (FACS) purified cells from EBs showed that defini
213 ative cells, and fluorescence-activated cell sorter (FACS) sorting for Ly-6A/E+Kit+ cells.
214 tein (GFP) and a fluorescence-activated cell sorter (FACS) to perform genetic selection.
215 ducing clones by fluorescence-activated cell sorter (FACS) to reduce screening effort.
216 ransferase (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and inflam
217 n was assayed by fluorescence-activated cell sorter (FACS), and the expanded T-cell cultures produced
218  assessed with a fluorescence-activated cell sorter (FACS), cell adhesion, and fluorescence microscop
219  were examined by fluorescent activated cell sorter (FACS), reduction of ferricytochrome C, and bioas
220               By fluorescence-activated cell sorter (FACS), there were less CD4+ T cells in naive TG
221    Here we use a fluorescence-activated cell sorter (FACS)-based approach to investigate expression o
222 d a differential fluorescence-activated cell sorter (FACS)-based sorting strategy using an Env trimer
223 -PCR analysis of fluorescence-activated cell sorter (FACS)-purified CD4+ NK1.1+ T lymphocytes.
224 nts who received fluorescence activated cell sorter (FACS)-sorted autologous CD34+ hematopoietic prog
225 act coculture of fluorescence-activated cell sorter (FACS)-sorted bone marrow (BM) CD34(+)CD38- cells
226 ents of 200 male fluorescence-activated cell sorter (FACS)-sorted CD34(+)lin(-) cells were sacrificed
227 array studies on fluorescence-activated cell sorter (FACS)-sorted cells and microdissected GC cells.
228 ned by QA-PCR of fluorescence-activated cell sorter (FACS)-sorted peripheral blood from 20 seropositi
229 aries by using a fluorescence-activated cell sorter (FACS).
230 ntibodies, or by fluorescence-activated cell sorter (FACS).
231 tion of signal propagation and act as signal sorters, filters, and synchronizers.
232 scence and separated using a high-speed cell-sorter for further processing.
233               Here we demonstrate an optical sorter for microscopic particles that exploits the inter
234  fast enough to provide a decision to a cell sorter for real-time separation of individual target cel
235 SA26 tissues and fluorescence-activated cell sorter-Gal analysis of hematopoietic cells demonstrates
236 versity of California Santa Cruz (UCSC) Gene Sorter has been created as a gene-based counterpart to t
237                                         Cell sorters have undergone dramatic technological improvemen
238  were interrogated in the DEP-activated cell sorter in a continuous-flow manner, wherein the electric
239 ure assays or by fluorescence-activated cell sorter in the context of their therapeutic or diagnostic
240 high-throughput absorbance-activated droplet sorter increases the effective sensitivity of absorbance
241 tion of cells by fluorescence-activated cell sorter indicate that there is a precise correlation betw
242 er pairs via the fluorescence-activated cell-sorter instrument.
243                 The quadrupole magnetic cell sorter is a form of split-flow thin-channel (SPLITT) sep
244                         This integrated cell sorter is incorporated with various microfluidic functio
245  capabilities, although their use as droplet sorters is poorly defined and underutilized.
246 ised on geneticin-supplemented food, the sex-sorter line establishes 100% positive selection for fema
247  CD90.2 antibody and Magnetic Activated Cell Sorter (MACS) technique, we successfully purified Thy-1
248 (+)-enriched cells were purified on the cell sorter (mean purity, 97.7% +/- 2.4%; n = 7), and examine
249  Hi-D (11-color) fluorescence-activated cell sorter method in which we covalently couple a fluorescen
250  microfabricated fluorescence-activated cell sorter (microFACS) for sorting various biological entiti
251       This micro fluorescence-activated cell sorter (microFACS) uses an infrared laser to laterally d
252 e examined using fluorescence-activated cell sorter, mixed lymphocyte reaction, enzyme-linked immunos
253 multitarget dielectrophoresis activated cell sorter (MT-DACS) chip.
254 tem, the multitarget magnetic activated cell sorter (MT-MACS), which makes use of microfluidics techn
255 rast, commercial fluorescence-activated cell sorters offer superior speed, sensitivity, and multiplex
256 populations by a fluorescence-activated cell sorter, placed in culture, and then reanalyzed by flow c
257 eome analysis of fluorescence-activated cell sorter-purified beta-cells, tissue-comparative Western b
258 maHV68 genome in fluorescence-activated cell sorter-purified cell populations.
259  interactions based on transcriptome data of sorter-purified niche cells and hematopoietic stem and p
260 eveloped by us, the quadrupole magnetic flow sorter (QMS).
261 nnular channel geometry of the magnetic cell sorter require that a new strategy be developed for opti
262 icroscopy and by fluorescence-activated cell-sorter scanner.
263 od that uses the fluorescence-activated cell sorter selection of low Hoescht 33342/low Rhodamine 123
264  The data reveal that dielectrophoretic cell sorters should have the ability to discriminate between,
265 ry, selecting by fluorescence-activated cell sorter single cells displaying low PAI promoter activity
266 atter and side-angle light scatter in a cell sorter, singly infected RBCs can be isolated and automat
267 ng this assay to fluorescence-activated cell sorter-sorted cell populations, we found that the Lin(-)
268 egulated between fluorescence-activated cell sorter-sorted clonal B cells from the 3 disease groups.
269 tion analysis of fluorescence-activated cell sorter-sorted CTCs also unraveled different cytogenetic
270  was analyzed by fluorescence-activated cell sorter staining, Western blotting with the monoclonal an
271 ound anti-Gal by fluorescence-activated cell sorter, suggesting that these three GTs are alpha 1,3 GT
272 ined in vitro by fluorescence-activated cell sorter, T-cell proliferation assays, enzyme-linked immun
273                                By using flow sorters, T(SCM) cells can thereby be isolated efficientl
274 ing quantitative fluorescence-activated cell sorter technology, we found that DC-SIGN is highly expre
275 show that older children were more effective sorters than younger children and used efficient sorting
276     We demonstrate a high-speed microfluidic sorter that can isolate and immobilize Caenorhabditis el
277 in a two-stage, continuous-flow microfluidic sorter that separates antibody-binding target cells capt
278                 We demonstrate a three-input sorter that uses several AND gates and OR gates, as well
279 ontrast to previous absorbance-based droplet sorters that relied on single-wavelength absorbance in t
280  including BLAT, the Table Browser, the Gene Sorter, the Proteome Browser, VisiGene and Genome Graphs
281 r employs a highly miniaturized microfluidic sorter to deterministically select single cells of inter
282  Appropriate gates are constructed on a cell sorter to exclude dead cells and lineage (CD45(+)Ter-119
283 e assayed using a fluorescent-activated cell sorter to identify DiI-labeled reconstituted AMs, unlabe
284                        We have used the cell sorter to isolate mutant cells with constitutively high
285             It may also serve as a molecular sorter to preserve and reclaim normal albumin while allo
286 the malaria parasite; the method uses a cell sorter to rapidly isolate Plasmodium falciparum-infected
287 responsive enhanced GFP reporter, and a flow sorter to recover dominant modulators of reporter expres
288 , sorted using a fluorescence-activated cell sorter, to polarize IL-21(+)CXCL13(+) (IL-21-positive an
289 developed an integrated microfabricated cell sorter using multilayer soft lithography.
290  was analyzed by fluorescence-activated cell sorter, using one of the following antibodies: anti-OX3,
291 troduce the UV-vis spectra-activated droplet sorter (UVADS) for high-throughput label-free chemical i
292 as quantified by fluorescence-activated cell sorter, varied inversely with disease progression.
293 l populations, a fluorescence-activated cell sorter was used to detect, sort, and enrich fibroblast p
294 ter counter with a dc-dielectrophoretic cell sorter, we demonstrate simultaneous on-chip cell separat
295                    Using a Drosophila embryo sorter, we isolated enough homozygous twist mutant embry
296 r, using a device referred to as an OAM mode sorter, we show that OAM modes can be (de)multiplexed ov
297 fic migration directions in the constriction sorter were induced for long SWNTs (>=1000 nm) with nega
298 ial microfluidic (trapezoidal cross-section) sorter with enhanced separation resolution and demonstra
299 s and target enrichment with the 3D particle sorter within a few minutes, downstream analyses were ab

 
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