ライフサイエンスコーパス: FACS

1 FACS analysis and CD40L binding studies revealed unchang

2 FACS analysis of mouse spleen cells revealed proinflamma

3 FACS analysis revealed that IL-10 production was associa

4 FACS analysis showed that transferrin-mediated targeting

5 FACS analysis was performed on PBMCs and intrahepatic ly

6 FACS and electron microscopy analyses showed that GKY25

7 FACS has high inter-observer variability and subjectivit

8 FACS identified prominent NPS receptor expression in PVN

9 FACS measurements reveal the ability to discriminate emp

10 FACS sorting from Hoxb7/enhanced green fluorescent prote

11 FACS sorting showed that these CD16(hi) eosinophils were

12 FACS-sorted adult human ductal cells clonally expanded a

13 FACS-sorted and enriched KIR2DS2(+) NK cell subpopulatio

14 FACS-sorted endothelial cells isolated from regenerating

15 A FACS-based shRNA screen identified several MMS genes as

16 A FACS-based sorting of the library beads allowed recovery

17 h standard molecular biology equipment and a FACS machine.

18 We also describe a FACS-based method that is used subsequently to obtain hi

19 We employed a FACS-based screen for Nlrp3-dependent cell death, using

20 Here, we establish a FACS-based HaloTag-LC3 autophagosome completion assay to

21 We have used a FACS-based genome-wide screening system to identify tran

22 aptamers are then further optimized using a FACS-based directed evolution approach.

23 a semi-rational engineering approach using a FACS-based screening/counterscreening strategy to genera

24 We used a "FACS-array" approach to identify 18 genes for transmembr

25 Therefore, our integrated acoustofluidic FACS device is demonstrated to achieve two-way cell sort

26 Our acoustofluidic FACS device uses the "microfluidic drifting" technique t

27 Applying detailed serology, advanced FACS analysis, and systems biology, we discovered that a

28 n addition, the use of reporter genes allows FACS-purification and tracking of cells that have had mu

29 tracellular lipids with BODIPY(505/515), and FACS-based isolation of top 0.5% lipid-rich E. gracilis

30 ets were confirmed via lumi-aggregometry and FACS analysis for P-selectin and LAMP-1 exposure.

31 oved multiple displacement amplification and FACS, to obtain genomic sequences and cell size informat

32 were independently enumerated using ARCA and FACS within 24 hours of blood sample collection, and p<0

33 was determined by RT-PCR, Western blot, and FACS, and enzymatic activity by HPLC.

34 PAD4 activity was increased by diabetes, and FACS detection of histone citrullination, together with

35 Confocal images and FACS demonstrated a strong association and co-localizati

36 pancreatic islets by immunofluorescence and FACS.

37 cells, Mac-2/Galectin-3 immunostaining, and FACS (fluorescence-activated cell sorting) analysis (CD4

38 and mouse lung tissues, immunostaining, and FACS analysis to identify transcriptional and signaling

39 hromatin state maps, custom microarrays, and FACS purification of the subventricular zone lineage, we

40 ts such as laser-capture microdissection and FACS, Retro-TRAP is a high-throughput methodology that r

41 Immunofluorescence microscopy and FACS analysis were used to determine levels of alphavbet

42 switching to IgE were analyzed by RT-PCR and FACS.

43 e epithelia can be isolated by pipetting and FACS sorting into a population of corneal epithelial-lik

44 Ultrastructural, proteomic and FACS analyses of Atg16L-positive vesicles reveal that 30

45 on laser microdissected tubular segments and FACS-sorted renal immune cells and identified the S3 pro

46 Immunofluorescent staining and FACS analysis show that AAA lesion neutrophils express F

47 nversion via three consecutive targeting and FACS events.

48 proliferation assay, caspase activity assay, FACS and Western blot.

49 ochemistry, paracellular permeability assay, FACS, cytokine assay, and immunofluorescence microscopy,

50 re, using immunostaining and Tf-flux assays, FACS analysis, and fluorescence imaging, we report local

51 rs (hOPCs) directly, we used CD140a/O4-based FACS of human forebrain and microarray to hOPC-specific

52 oides pteronyssinus (Der p) allergen, before FACS phenotyping and co-culture with allogeneic CD4+ T c

53 to our knowledge, of BONCAT-FISH and BONCAT-FACS within an environmental context, we probe the trans

54 fluorescence-activated cell sorting (BONCAT-FACS) for subsequent genetic analyses.

55 We conclude that BONCAT-FACS is effective for interrogating the active fraction

56 s showed no signs of impaired viability, but FACS revealed significantly reduced TH immunoreactivity

57 Cs, as detected in Myf5(nLacZ/+) mice and by FACS sorting, and this effect was inhibited by Ang II AT

58 nescence-associated cell-surface antigens by FACS analysis and a newly developed cell-based ELISA.

59 erent pneumococcal serotypes, as assessed by FACS and immunofluorescence analysis.

60 tobrush-derived CD4+ T cells was assessed by FACS.

61 treatment by PV sera, which was confirmed by FACS analysis.

62 These data were corroborated by FACS measurements showing a decrease of CD11b(+)/CD45(hi

63 ree tumors, aneuploid cells were detected by FACS.

64 Analysis of isolated tubular epithelia by FACS from bigenic SLC34a1-CreERt2; R26tdTomato proximal

65 ines OS-17, OS-33 and OS-31 was evaluated by FACS.

66 , we assessed differential RNA expression by FACS-purified adult astrocytes and, on that basis, evalu

67 o-labeled S. aureus bioparticles followed by FACS analysis.

68 Tek-tdTomato reporter mice to isolate GEC by FACS and performed transcriptome analysis on them from W

69 nflammation was quantified histologically by FACS and gene expression analysis.

70 CD44(+)CD24(lo)CD166(+) cells, isolated by FACS from mouse small intestine and colon, expressed hig

71 lR1(+) neural progenitors can be isolated by FACS or magnetic sorting (MAC) which give rise to dopami

72 -seq libraries, single cells are isolated by FACS sorting, lysed and digested by MNase.

73 , and memory tonsil B cells were isolated by FACS, and their capacities for IL-4 and anti-CD40 signal

74 eloped a protocol for hair cell isolation by FACS.

75 via high-throughput single-cell isolation by FACS.

76 Phosphorylated Stats were measured by FACS before and after stimulation with increasing doses

77 and mitochondrial potential was measured by FACS-based JC1 staining.

78 cellular cytokine production was measured by FACS.

79 detected on resting neutrophil membranes by FACS analysis, and expression levels significantly incre

80 isolation of pure nonactivated microglia by FACS.

81 of cytokine-producing cells was performed by FACS.

82 limbus and their subsequent purification by FACS.

83 es on regenerating support cells purified by FACS.

84 slet isolation, dispersion and separation by FACS for EGFP resulted in an 86% pure population of alph

85 take as single-stranded T-oligo, as shown by FACS analysis.

86 ei are isolated from specimens and sorted by FACS, cDNA libraries are constructed and RNA-seq is perf

87 d donor buffy coats, and ILCs were sorted by FACS.

88 )/eGFP and smMHC/Cre/eGFP mice and sorted by FACS.

89 editing coupled to a cell selection step by FACS to identify regulators of SQSTM1.

90 to isolate L-histidine-producing strains by FACS, showing that TR engineering towards a more focused

91 fic GFP fusion protein to isolate tetrads by FACS and (ii) molecular barcodes that are read during ge

92 cells for accumulation of acidic vesicles by FACS sorting.

93 Notably, single cell FACS technology was applied to further promote virus pur

94 Whole cell-FACS is more similar to nuclear-FACS than RiboTag, but c

95 matically comparing nuclear-FACS, whole cell-FACS, and RiboTag affinity purification from D1- and D2-

96 We proved via </= five-colour FACS that the manipulation of this in vitro model allowe

97 Subsequently, four-colour FACS verified the ability to determine the biochemical e

98 Importantly, our combined FACS and single-cell RNA sequencing (scRNA-seq) workflow

99 viability drops by 35-45% using a commercial FACS machine, while the cell viability only drops by 3-4

100 Competitive FACS increased the frequency of hapten-specific scFvs in

101 lay system and a newly developed competitive FACS procedure was employed to select rare hapten-specif

102 ncept, this study demonstrates that coupling FACS with WGA and microarrays is a promising tool to exp

103 be readily detected in 3D organoid cultures, FACS analysis and in vivo tumour models.

104 Current FACS software requires the user to define sorting gates

105 sil B cells were analyzed by flow cytometry (FACS) and cultured with IL-4 and anti-CD40 to induce CSR

106 sue barrier via multi-colour flow cytometry (FACS).

107 d monocytes was evaluated by flow cytometry (FACS).

108 Our findings demonstrate FACS robustly detects perturbations of bacterial cell sh

109 r, studies here that couple high-dimensional FACS sorting with large-scale quantitative IgH deep-sequ

110 ChIP-seq on distinct subtypes of Drosophila FACS-purified NSCs and their differentiated progeny to d

111 , we used complementary approaches employing FACS coupled with quantitative RT-PCR, a validated GLP-1

112 Here we describe 'enhancer-FACS-seq' (eFS) for highly parallel identification of ac

113 These results were obtained by evaluating FACS-based side population (SP), autofluorescence (AF+)

114 On postmortem examination, FACS-based enumeration of intracranial tumor-infiltratin

115 First, FACS was successfully applied to a D. mccartyi isolate a

116 -9% cell loss compared to ~70% cell loss for FACS.

117 nd that anti-AOC3 antibodies can be used for FACS sorting of myofibroblasts obtained by nonenzymatic

118 igh-performance, portable, and user-friendly FACS instrument.

119 -ISL1 antibodies and chromatin extracts from FACS-purified SAN cells demonstrated that ISL1 directly

120 Gene profiling was generated from FACS-purified neurons leading to the identification of n

121 Furthermore, FACS may introduce bias but has not been benchmarked gen

122 e use of specific and expensive labels (e.g. FACS or MACS).

123 atopoietic cells with high purity through IE-FACS and profile them via aCGH analysis.

124 and fluorescence-activated cell sorting (IE/FACS), a technique previously used for isolating circula

125 Combining CD30 to SSEA4 and TRA-1-81 in FACS greatly enhanced specificity and efficiency of hiPS

126 miR-215 expression is depleted in FACS-enriched cancer stem cells compared with unsorted s

127 nflammatory cytokine IL-1beta was greater in FACS-isolated microglia than in brain-invading monocytes

128 col for the isolation of bona fide hiPSCs in FACS-based selection using an optimized combination of c

129 hown to bind this heparin-binding peptide in FACS analysis, and the interaction was shown to be with

130 using a combination of approaches, including FACS analysis, time-lapse imaging, immunofluorescence mi

131 including GM-CSF, detected by intracellular FACS and ELISA.

132 d dendritic cells (DCs) and freshly isolated FACS-purified ILCs, we demonstrate that IL-23 and IL-1 s

133 NA sequencing), its interactions with Keap1 (FACS), Keap1-Nrf2 interactions, and transcription of the

134 l-specific transcriptomics without laborious FACS-based cell sorting or biochemical isolation of the

135 Although methods like FACS and FISH-FC can characterize and isolate cells from

136 MDE-FACS allowed the identification of human butyrylcholines

137 The microscale FACS-Chip-LCMS workflow demonstrated high cellular enric

138 Overall the microscale FACS-Chip-LCMS workflow has shown effectiveness in effic

139 show dTn-Seq compatibility with microscopy, FACS and investigations of bacterial cell-to-cell and ba

140 strate is cleaved are isolated by multicolor FACS with fluorescently labeled antiepitope tag antibodi

141 ress this, the current study used multicolor FACS of disaggregated tumor to systematically characteri

142 ng a combination of biochemical, mutational, FACS, and single molecule super-resolution imaging appro

143 estive of a trend in ARMD using ARCA but not FACS.

144 Nuclear-FACS-seq generates the most differentially expressed gen

145 ese gaps by systematically comparing nuclear-FACS, whole cell-FACS, and RiboTag affinity purification

146 Whole cell-FACS is more similar to nuclear-FACS than RiboTag, but captures aspects of both.

147 duced CD38(+) hPGCLCs [ approximately 43% of FACS-sorted embryoid body (EB) cells] from primed-state

148 in efficiently preparing limited amounts of FACS enriched cells in an online manner for proteomic LC

149 RNA-Seq analyses of FACS-isolated wild-type and Six2(GFP(+)) CM cells reveal

150 RNA-sequencing (RNA-seq) analyses of FACS-purified cells from ISL1-deficient SANs revealed th

151 Single-cell gene expression analyses of FACS-sorted macrophages revealed that these subpopulatio

152 Global transcriptomic analysis of FACS-isolated adipocytes confirmed the presence of disti

153 We carried out a transcriptomic analysis of FACS-isolated cells from DeltaSox2-eGFP, Neurog1-eGFP BA

154 RNA-sequencing analysis of FACS-purified Abcc8(-/-) beta-cells confirmed an increas

155 Transcriptome analysis of FACS-purified choroid plexus epithelial cells also predi

156 Analysis of FACS-purified MDSCs recovered from S. aureus biofilms re

157 We used microChIP and qPCR assays of FACS-purified cells to track changes in the epigenetic s

158 this study, we have compared the behavior of FACS-sorted CD56(dim)CD57(-)KIR(-)NKG2A(+) (NKG2A(+)) an

159 Following multiple iterations of FACS, cells and progeny virions were shown to display hi

160 ws clonal expansion and self-organization of FACS-sorted bronchioalveolar stem cells (BASCs) upon co-

161 Phenotyping by RT-PCR of FACS-sorted CD45RO(hi) T cells secreting IL-10 in respon

162 ridization, and most importantly ATAC-Seq of FACS-isolated nuclei, to show that cardiac ECs actively

163 16S rDNA pyrotag sequencing of FACS-sorted cells indicated that PUT- and SPD-transformi

164 Transcriptomes of FACS-purified alpha-, beta-, and delta-cells using bulk

165 Cellular transfer of FACS-purified MCs from allogeneic donors into recipients

166 In this study, FAIRE-seq on FACS-purified midline cells was performed and the midlin

167 The results from the online FACS-Chip-LCMS workflow starting from 5000 enriched cell

168 To assess the performance of the online FACS-Chip-LCMS workflow, 5000 fluorescent labeled cells

169 ed by aggregometry, thromboxane B2 assay, or FACS.

170 use and human prostate cells (either bulk or FACS-sorted single luminal and basal cells), metastatic

171 , combining sampling by limiting dilution or FACS, with imaging and high throughput at competitive co

172 ein is done by immunoassays such as ELISA or FACS that are susceptible to the sequence variation and

173 Corroborating this hypothesis, our FACS, in vitro, and in vivo data demonstrate that entire

174 ted MV, immunoblotting, quantitative RT-PCR, FACS analysis, and enzymatic assays, we show that miR221

175 A dual polychromatic FACS-based biomarker-labeling system based on the IL4-eG

176 s S phase in an unperturbed cell population; FACS is used to isolate replicating and non-replicating

177 Here we present FACS studies of peripheral blood mononuclear cells colle

178 fic intracellular immunolabelling protocols, FACS separation of interphase and mitotic cells, includi

179 Here, we describe a rapid FACS purification strategy to simultaneously isolate pri

180 Second, FACS enrichment of cells expressing nucleases linked to

181 alyses of fluorescent-activated cell sorted (FACS) DRG neurons confirmed that this 3'-UTR-extended va

182 ata from fluorescence-activated cell sorted (FACS) SCs and macrophages from wild-type and mutant nerv

183 Fluorescence-activated cell sorter (FACS) analysis of cell permeability showed the efficienc

184 sured by fluorescence-activated cell sorter (FACS) analysis.

185 SAs) and fluorescence-activated cell sorter (FACS) binding analyses, our results show that extended L

186 se (ALT), fluorescent-activated cell sorter (FACS), analysis of liver infiltration and inflammation,

187 scence- and magnetic-activated cell sorting (FACS and MACS, respectively), to more specialized approa

188 Fluorescence-activated cell sorting (FACS) allows for rapid enumeration of metabolically acti

189 Fluorescence-activated cell sorting (FACS) analysis indicated significant increases in number

190 d using fluorescence-activated cell sorting (FACS) analysis of inflammatory marker expression (PECAM-

191 Fluorescence activated cell sorting (FACS) analysis revealed that re-expression of miR-23b in

192 lot and fluorescence activated cell sorting (FACS) analysis revealed that silencing of Scrib reduced

193 CR) and fluorescence-activated cell sorting (FACS) analysis were used to investigate lymphocyte frequ

194 ermore, fluorescence-activated cell sorting (FACS) and confocal microscopy assays demonstrate that st

195 Fluorescence-activated cell sorting (FACS) and confocal microscopy showed that the designed a

196 s using fluorescence activated cell sorting (FACS) and control cellular functions with light sensitiv

197 nd used fluorescence-activated cell sorting (FACS) and fiber-optic array scanning technology (FAST) t

198 We use fluorescence-activated cell sorting (FACS) and genomic sequencing to assign taxonomy to BONCA

199 ilizing fluorescence-activated cell sorting (FACS) and high-throughput microscopy to identify L. mono

200 Fluorescence-activated cell sorting (FACS) and histopathology studies showed that the observe

201 ds like fluorescence-activated cell sorting (FACS) and magnetic-activated cell sorting (MACS) are und

202 such as Fluorescence Activated Cell Sorting (FACS) and multiplex immunofluorescence.

203 ows for fluorescence-activated cell sorting (FACS) and single-cell deposition and thereby eliminates

204 Fluorescence-activated cell sorting (FACS) and subsequent microarray analysis of sensory neur

205 Fluorescence-activated cell sorting (FACS) confirmed that donor- and host-specific levels of

206 gy with fluorescence-activated cell sorting (FACS) demonstrated that micropallet arrays offered enhan

207 fluidic fluorescence activated cell sorting (FACS) device that simultaneously performs on-demand, hig

208 without fluorescence-activated cell sorting (FACS) enrichment of haploid cells.

209 city of fluorescence activated cell sorting (FACS) for multicolor sorting to simultaneously screen fo

210 ties of fluorescence-activated cell sorting (FACS) from fluorescence intensity profiles of cells to m

211 ning by fluorescence activated cell sorting (FACS) is a common task in protein engineering and direct

212 ysis, a fluorescence-activated cell sorting (FACS) method was developed in this study to separate D.

213 tion by fluorescence-activated cell sorting (FACS) of c-kit(+) hematopoietic progenitor cells from mi

214 ed with fluorescence-activated cell sorting (FACS) of millions of aptamers expressed in Escherichia c

215 ants by fluorescence-activated cell sorting (FACS) of pooled mutants stained with the lipid-sensitive

216 ludes a fluorescence activated cell sorting (FACS) procedure that results in no perturbation of trans

217 fied by fluorescence-activated cell sorting (FACS) protocol resulting in >= 99% purity and >= 95% via

218 ered by fluorescence-activated cell sorting (FACS) reveals that the phylogenetic composition of the a

219 ed with fluorescence-activated cell sorting (FACS) to allow for efficient isolation of cell populatio

220 on, and fluorescence-activated cell sorting (FACS) to analyze intestinal epithelial cells isolated fr

221 ry with fluorescence-activated cell sorting (FACS) to enrich a transposon library for bacterial cells

222 hen use fluorescence-activated cell sorting (FACS) to individually measure the relative affinities of

223 use of fluorescence-activated cell sorting (FACS) to perform a high-throughput analysis of gut micro

224 mployed fluorescence-activated cell sorting (FACS) to sort for cells that are recognized by trimer cr

225 we used fluorescence-activated cell sorting (FACS) to sort the glial and vascular cells from the brai

226 fied by fluorescence-activated cell sorting (FACS) using endogenous expression of enhanced green fluo

227 mbining fluorescence-activated cell sorting (FACS) with annexin V staining.

228 ysis by fluorescence-activated cell sorting (FACS), a CRISPR-Cas9-mediated approach was used to attac

229 rted by fluorescence-activated cell sorting (FACS), and V(D)J transcripts are amplified by RT-PCR.

230 otting, fluorescence-activated cell sorting (FACS), enzyme-linked immunosorbent assay, immunofluoresc

231 grating fluorescence activated cell sorting (FACS), focused ultrasonication, microfluidics, immobiliz

232 ed with fluorescence-activated cell sorting (FACS), so that individual cells, including stem cells, c

233 nsitive fluorescence-activated cell sorting (FACS)-based assay, which allowed us to enumerate metasta

234 r and a fluorescence-activated cell sorting (FACS)-based transposon screen, we find that deletion of

235 ling of fluorescence-activated cell sorting (FACS)-purified murine PCs at various stages of their pos

236 Fluorescence-activated cell sorting (FACS)-purified Tbx18-expressing cells behaved as MSCs in

237 qPCR on Fluorescence Activated Cell Sorting (FACS)-sorted tnfa(+) and tnfa(-) macrophages showed that

238 ined by fluorescence activated cell sorting (FACS).

239 is with fluorescence-activated cell sorting (FACS).

240 fied by fluorescence activated cell sorting (FACS).

241 ssed by fluorescence-activated cell sorting (FACS).

242 ing via fluorescence-activated cell sorting (FACS).

243 mice by fluorescence-activated cell sorting (FACS).

244 CR, and fluorescence-activated cell sorting (FACS).

245 t deficiency by flow-activated cell sorting (FACS).

246 ssed by fluorescence-activated cell sorting (FACS).

247 ained by fluorescent activated cell sorting (FACS).

248 on with fluorescence-activated cell sorting (FACS).

249 lated by fluorescent activated cell sorting (FACS).

250 rted by fluorescence activated cell sorting (FACS).

251 scence- and magnetic-activated cell sorting (FACS/MACS).

252 -based (fluorescence-activated cell sorting; FACS) strategy to detect and quantify pyroptosis in vivo

253 The Fasa Cohort Study (FACS) population (Fars Province, Iran) was used to colle

254 /CK(pos)/CD45(neg)/DAPI(pos)) and subsequent FACS sorting.

255 y, MACS processing was 4-6 times faster than FACS for single, low proportion samples but took similar

256 ate increased cell numbers in less time than FACS may prove valuable in both basic science and transl

257 trospective cohort analysis of data from the FACS (follow-up after colorectal cancer surgery) trial a

258 Subsequent application of the FACS and WGA protocols to two enrichment cultures contai

259 HDC expression within these FACS-separated cells was found to coincide with other ma

260 High-throughput FACS screening of cellular picoreactors has the potentia

261 Thus, FACS provides a method to isolate and enrich human sperm

262 e performed in any laboratory with access to FACS, robotic and high-throughput-sequencing facilities.

263 The probes were effectively applied to FACS analysis of microglial cells derived from a mouse m

264 rate ALPL+ vs. ALPL- cell splits compared to FACS when ALPL+ cells were present in larger proportions

265 t protein (eGFP) and cell surface markers to FACS-isolate DeltaSox2-eGFP(+) GBCs, Neurog1-eGFP(+) GBC

266 otoxic against GBM and K562, and, similar to FACS-sorted or gated KIR2DS2(-) NK cells, significantly

267 sed the objective, anatomically-based tools, FACS and DogFACS (Facial Action Coding Systems), to quan

268 nic mouse motor neurons isolated by a unique FACS technique.

269 We therefore used FACS sorting to show that, in mixed neuron glia co-cultu

270 nt cell populations within an organ, we used FACS to dissect GFP-marked cells from Arabidopsis roots

271 Using FACS and RT-PCR, we examined the phenotype of generated

272 Using FACS to stratify IPF MPCs based on CD44 expression, we d

273 Using FACS-assisted shRNA screens, we identified the cell-surf

274 Using FACS-isolated populations, we demonstrate that bronchioa

275 estingly, CD34(+)VEGR2(+) EPC analysis using FACS did not produce similar results (p = 0.94).

276 sed L-DOPA production in S. cerevisiae using FACS enrichment of an enzyme-coupled biosensor for L-DOP

277 ce of RIF, and bacilli were enumerated using FACS.

278 riants with reduced affinity for c-FMS using FACS.

279 ibodies was concomitantly investigated using FACS analysis, and the results indicated excellent cell

280 ociated Thy1-eYFP neurons are isolated using FACS.

281 In this study, using FACS-based isolation and microarray analysis, we identif

282 ting outcomes and reducing effort when using FACS.

283 rofiling, immunohistochemistry and annexin V FACS staining.

284 m a fusion mixture as single-cell clones via FACS.

285 We demonstrated via FACS that EpCAM is expressed by human spermatogonia but

286 generated LECs, which were then isolated via FACS-sorting with LYVE-1 and PODOPLANIN.

287 with human iPS cell culture and sorting via FACS will be of benefit for researchers performing this

288 We FACS-purified and transcriptionally profiled basal and l

289 Finally, we FACS isolate foetal HHyPs and confirm their hybrid proge

290 n which HCs express GFP driven by Pou4f3, we FACS purified a population of HCs to analyze and compare

291 nhanced binding over the parental clone were FACS-sorted and cloned.

292 Additionally, when FACS-isolated subpopulations of myeloid cells were trans

293 poxic murine model of PH in combination with FACS to quantify and isolate lung macrophages from two c

294 ow molecular enrichment can be combined with FACS to efficiently target ultra-rare cell types, such a

295 Combined with FACS, SPARK enabled 51 fold enrichment of PPI-positive o

296 c mice with GFP-expressing HCs, coupled with FACS sorting and tandem mass spectrometry, to define the

297 vitro differentiation system initiated with FACS-sorted adult ductal progenitor-like cells, and (v)

298 rs ( approximately 200) when integrated with FACS.

299 ination of droplet-generating machinery with FACS followed by next-generation sequencing and liquid c

300 (SHP2) domain-specific reporter, paired with FACS and RNA sequencing, we assayed the transcriptome of