ライフサイエンスコーパス: stain

1 expressing Kv3.1b were very rare and weakly stained.

2 assessed for necrosis with hematoxylin-eosin staining.

3 nfections without organisms detected by Gram staining.

4 hen compared to optimized immunofluorescence staining.

5 esolution without the need for sectioning or staining.

6 neutrophils and macrophages by histological staining.

7 erase chain reaction and immunohistochemical staining.

8 t microscopy after Maurits, Scarlet and Blue staining.

9 42 staining, annexin V/PI staining, and JC-1 staining.

10 milar human-based score on hematoxylin-eosin staining.

11 ether (18)F-FDG uptake correlates with GLUT1 staining.

12 probe coupled with cardiac-specific antibody staining.

13 ina was examined using Hematoxylin and eosin staining.

14 diffusely for PD-L2 and showed sparse PD-L1 staining.

15 ools, was examined by intracellular cytokine staining.

16 on, Western blotting, and immunofluorescence staining.

17 arts for 2,3,5-triphenyltetrazolium chloride staining.

18 P-biotin nick end labeling assay and Hoechst staining.

19 transferase-mediated dUTP nick-end labeling staining.

20 tion of synapses from conventionally en-bloc stained 3D electron microscopy image stacks.

21 the root hairs by 3,3-diaminobenzidine (DAB) stain 72h after bacterial inoculation.

22 were derived from carotid endarterectomy and stained against P2X7.

23 Immunofluorescence staining against AstA, AT, and TK in the brain revealed

24 The immuno-staining analysis also showed that topoisomerase II is t

25 en determined via Annexin V/Propidium iodide stain and flow cytometry.

26 ath was measured by Hoechst/propidium iodide staining and activation of caspase-3.

27 Congo red staining and apple green birefringence demonstrated vitr

28 transcription, as shown by propidium iodide staining and BrUTP incorporation.

29 emonstrated less senescence by X-beta-Gal SA staining and by lower expression of p16.

30 by senescence-associated beta-Galactosidase staining and by Western blot analysis of p16.

31 gh alanine scanning, immunofluorescence cell staining and co-immunoprecipitation, we define a critica

32 a acquired from different sources, different staining and cutting protocols and different scanners.

33 d mononuclear cells (PBMCs) by intracellular staining and dual-secretion assay.

34 Analysis of Masson trichrome staining and fibrotic marker protein and mRNA expression

35 as determined by indirect immunofluorescence staining and flow-cytometric analysis.

36 Microtome sectioning, differential staining and fluorescence microscopy were used to visual

37 va of the right eye for periodic acid-Schiff staining and from the left eye for MUC5AC mucin immunost

38 s and PSMA expression in immunohistochemical staining and generate a cutoff value for differentiation

39 yuridine (BrdU) assay, propidium iodide (PI) staining and growth curves, and blocks cell migration ba

40 Heart tissue was evaluated with vital staining and histologic examination.

41 Alizarin red staining and immunohistochemistry of GFP and osteocalcin

42 Consistently, immunohistochemical staining and in vitro binding assays showed that apoE co

43 d by morphometric quantitation of Sirius Red staining and increased mRNA levels of profibrotic genes,

44 iver was established by immunohistochemistry staining and mass spectrometric analysis.

45 By combining fluorescent staining and microspectroscopy with software-based spect

46 caused by microneedle penetration following staining and optical imaging.

47 ere reexamined by periodic acid-Schiff (PAS) staining and PCR to identify undiagnosed amoebic appendi

48 non-mineralised tissue can be enhanced using staining and phase contrast techniques.

49 rein, we utilized immunohistochemistry (IHC) staining and public microarray data analysis showing tha

50 Furthermore, phalloidin staining and reactive oxygen species estimation of Wnt5a

51 l fibrosis, as determined by Picrosirius Red staining and Second Harmonic Generation (SHG) Microscopy

52 phism (rs13266634) have decreased proinsulin staining and susceptibility to T2DM.

53 EETs and S aureus by using immunofluorescent staining and the PNA-Fish assay, respectively.

54 resent study, we employed immunofluorescence staining and Western blot analysis to assess the express

55 re than 300 tumors using immunohistochemical staining and western blot.

56 ity, compatibility with common histochemical stains and suitability for analysis of decade-old materi

57 ate protists), including 'live' (Rose Bengal stained) and dead tests, in 5 cores (0-1 cm layer, >150-

58 hocytes by double immunohistochemistry (PCNA-staining) and flow cytometry (BrdU incorporation) reveal

59 onjunction with immunohistochemistry, myelin staining, and a novel three-choice, reversal-learning ta

60 and silver methenamine, and picrosirius red staining, and CD31 and CD34 immunohistochemistry were ap

61 glycan deposition as assessed by Alcian blue staining, and gene expression of key anabolic proteins b

62 in reaction, dual-labeling immunofluorescent staining, and immunoassays.

63 assay, Hoechst 33342 staining, annexin V/PI staining, and JC-1 staining.

64 ndrial depolarisation was quantified by TMRE staining, and levels of DNA damage were compared in cell

65 electron microscopy (TEM) and Prussian Blue staining, and quantified using an iron specific colourim

66 mary epithelial proliferation, based on Ki67 staining, and suppressed tumor development.

67 drogenase (LDH) release assay, Hoechst 33342 staining, annexin V/PI staining, and JC-1 staining.

68 ELISA of cultured supernatants, and F-actin staining; apoptosis and efferocytosis by morphology and

69 ombined with a typical hematoxylin and eosin stain aspect defined a new HCA subgroup at a high risk o

70 olysis, cell viability, and AnnexinV-FITC/PI staining assays.

71 y of forensic evidence, including body fluid stains, at the scene of a crime.

72 icroscopic diagnosis of malaria using Giemsa-stained blood smears is the standard of care in resource

73 As determined by Sholl analysis of Golgi-stained brain sections, dendritic arbors of male hippoca

74 r stability, tear production, ocular surface staining, bulbar and limbal redness, tear volume, anteri

75 ified by cytology with hematoxylin and eosin staining but also provided molecular resolution through

76 d with 2-3 d for embryos or dissected tissue stains-but time is saved by eliminating the need for lar

77 al and counted pollen number per cm(2) after stained by Calberla solution and then classified main po

78 or two T. asahii strains, a clinical isolate stain CBS 2479 (T2) and an environmental isolate strain

79 The live/dead staining, cell proliferation assay and immunohistochemis

80 ic T cells, including intracellular cytokine staining, cell surface cytokine-capture assays, and stai

81 tly lower in PCA samples with fewer than 50% stained cells (n = 30; 2.81 +/- 2.35) than in samples wi

82 lular morphology, high percentage of annexin-stained cells and sub-G1 populations as well as nuclear

83 nning microscopy (CLSM) images (z-stacks) of stained cells and three types of scaffolds (i.e., spun c

84 (<2 years) had either low levels of the dual-stained cells or high levels of single-stained cells, an

85 ing intensity was mild, median percentage of stained cells was 20% +/- 14.24%, and median immunoreact

86 dual-stained cells or high levels of single-stained cells, and such patterns differentiated short fr

87 raphic atrophy (GA); and ultrastructural and staining characteristics of druse subtypes.

88 l transferase dUTP nick-end labeling (TUNEL) staining, circulating levels of alanine aminotransferase

89 pressed in the corticospinal tract and CHIT1 staining colocalised with markers of microglia (IBA1) an

90 Immunofluorescent staining confirmed that SFRP2 and FMO1 define cell types

91 athy was associated with increased caspase-3 staining, decreased CD3(+) T cells, and increased SIV-in

92 e capacity of fluorochrome-labeled avidin to stain degranulating cells.

93 Immunohistochemical staining demonstrated that Ebf3 and Meis2 showed a restr

94 ography, 2,3,5-triphenyltetrazolium chloride staining determined infarct size, and fluorescence-activ

95 Both tumors stained diffusely for PD-L2 and showed sparse PD-L1 stai

96 n situ, we identified a fluorescent dye that stains DNA with an osmiophilic polymer and selectively e

97 fter performing gammaH2AX immunofluorescence staining, DSBs were quantified with automated digital mi

98 , small-angle X-ray scattering, and negative-stain electron microscopy at neutral and acidic pH.

99 udy by dynamic light scattering and negative stain electron microscopy demonstrated that zinc ions in

100 ay diffraction data in solution and negative-stain electron microscopy images.

101 DeltaMBD-7B were characterized by a negative stain electron microscopy in the presence of ADP/MgCl2 S

102 ntext of P. falciparum CSP, we used negative-stain electron microscopy on a recombinant shortened CSP

103 h binding and inhibition assays and negative stain electron microscopy were performed.

104 ve the structure of this complex by negative stain electron microscopy, demonstrating that two copies

105 The complex was visualized by negative-stain electron microscopy, which revealed an architectur

106 MS), native mass spectrometry, and negative-staining electron microscopy to comprehensively characte

107 ed by immunohistochemistry and the number of stained elements were quantified.

108 polyacrylamide gel shift assay and negative-stain EM, we found that the prefusion conformational sta

109 culture, transfection, fixation, heavy-metal staining, embedding in resin, and EM imaging.

110 The method also works well for staining embryos, even late-stage embryos with cuticles,

111 atterns appear complementary, preferentially staining extramodular LCIC zones.

112 e and by the lack of antibodies suitable for staining FFPE tissue, primarily due to the inaccessibili

113 abel free monitoring methods without need to stain, fix, lyse, or fluorescent-tags are desirable in b

114 or Abeta and complement proteins but did not stain for conventional amyloid dyes, such as Thioflavin

115 tion of the target lesions, and tissues were stained for CD31 and KDR by IHC.

116 rinary bladder removed, then fresh-fixed and stained for immunoreactivity to calcitonin-gene-related-

117 numerated for acellular capillaries and were stained for oxidative damage markers using nitrotyrosine

118 2 in the stromal compartment as well as high staining for CXCR4 and CXCR7 in the epithelial compartme

119 bined with mass spectrometry and verified by staining for direct protein-protein interaction, we find

120 GCA-positive group, 3 patients had positive staining for herpes zoster antigen.

121 messenger RNA (mRNA) expression and positive staining for IL-6.

122 itu RNA hybridization combined with antibody staining for the HIV Gag protein.

123 on a red-blue-purple striped glass from the stained glass windows of the Sainte-Chapelle in Paris, F

124 tochemistry, GluR2-immunocytochemistry, Timm stain, glial fibrillary acidic protein-immunocytochemist

125 ers and 24 of 26 stained with Miller elastic stain had decreased elastic fibers.

126 ugh mutation load and PD-L1 immune cell (IC) staining have been associated with response, they lack s

127 lbumin) extravasation, and hematoxylin-eosin staining helped detect only scattered extravasation of r

128 The fluorescence staining identified the same particles as those found by

129 tribution of PLAG1 in the testis using X-gal staining; (ii) transcriptomic consequences of PLAG1 defi

130 re prominent in subsequent immunofluorescent staining images but not with classical hematoxylin and e

131 Double-staining immunohistochemistry showed CXCL9 co-localized

132 d and lesional morphea skin, and used double-staining immunohistochemistry to determine the cutaneous

133 alyzed by histology, immunoblots, phalloidin staining, immunohistochemistry, electron microscopy, and

134 ial growth factor (VEGF) level was highly co-stained in endothelial cells but not in macrophages in L

135 sing fSTREAM we assessed human breast tumors stained in vivo with fluorescent bevacizumab at microdos

136 correctly identified mislocalized or absent staining in 100% of the discovery cohort.

137 ithout intestinal disease, and levels of CD3 staining in all LSI animals strongly correlated with the

138 Immunohistochemical staining in an aromatase reporter mouse revealed that ma

139 t kidneys exhibited distinctly increased APA staining in areas of intact glomerular capillary loops.

140 ty activity in cell line A-431 and low green staining in cells.

141 odendrocyte density and myelin basic protein staining in CNS lesions.

142 Significantly lower Iba-1 and Perls' iron staining in DP1(-/-) and laropiprant-treated WT groups w

143 Overexpression of miR-10b increased Ki-67 staining in human organ-cultured corneas and proliferati

144 ted defects in autophagic flux and lysosomal staining in human samples of type 2 diabetes.

145 ance (R2 = 0.76-0.99) when using chromogenic staining in isogenic cell lines.

146 % were positive for KLF5 (defined as nuclear staining in more than 5% of tumor cells).

147 man tumor biopsies showed significant fibrin staining in nearly all tumor types evaluated.

148 ip to calcitonin gene-related peptide (CGRP) staining in the dorsal horn.

149 conditioning, we observed increased beta-gal staining in the nucleus accumbens (NAC) shell and dorsal

150 greater than 5% positive immunohistochemical staining in the respective cell populations.

151 RK-10 shows staining in the tumor regions of FFPE tissues where the

152 iated with an increased alkaline phosphatase staining in the XLH cultures.

153 al iron deposits; this was proven with Perls staining in two patients.

154 cytochrome c, and cleaved caspase-3 positive staining indicated that increased apoptosis involved a m

155 Histochemical GUS staining indicated that OsbHLH068 and AtbHLH112 share a

156 ical generator, was able to increase filipin staining indicating a link between ROS production and in

157 lesion exhibited increased filamentous actin staining, indicating active cell movement.

158 ze and a reduction in positive Fluoro-Jade B stained injured neurons and microglial activation.

159 gher BMP-2 release, and the majority of them stained intensely for alkaline phosphatase activity.

160 estinal segments studied revealed comparable staining intensities.

161 le amino acid substitution revealed that the staining intensity by anti-Valpha24 Abs depends on wheth

162 usting for age, sex, and BCC location, PD-L1 staining intensity in tumor cells increased with the num

163 In PN sections (n = 31), median staining intensity was mild, median percentage of staine

164 tumour cells with membrane staining of >/=1+ staining intensity), and evaluable disease, who had not

165 try (>/= 25% of tumor cells with at least 2+ staining intensity).

166 stricted CASZ1 staining or low nuclear CASZ1 staining is found in tumor samples from patients with po

167 lex instrumentation and expertise while only staining isolated areas.

168 tissue area was assessed in Masson trichrome stained kidney tissues.

169 uronan (XGA) epitope, and they become darkly stained large vesicles (LVs) after release from the Golg

170 d with human-derived peptides differentially stained leukocytes, suggesting peptide-dependent engagem

171 above resulting in a single 2D image of the stained manifold across which contrast is optimized and

172 t as follows: (i) extracting and mapping the stained manifold in each stack into a single 2D projecti

173 we compared lipid-, protein-, and RNA-based staining methods and developed a robust EV staining stra

174 Tissue microarray and microfluidics staining methods have emerged as powerful high throughpu

175 for histochemical studies (Masson trichrome stain), molecular markers of fibrosis (collagen and tran

176 Naive and activated T cells stained negative for C5aR2, whereas B cells from differe

177 e system positive inclusions (FTLD-UPS) that stained negatively for tau, TDP-43, and FUS.

178 Since Cajal's first drawings of Golgi stained neurons, generations of researchers have been fa

179 ely, and tartrate-resistant acid phosphatase staining notably was absent in the subarticular regions

180 umours (>/=25% of tumour cells with membrane staining of >/=1+ staining intensity), and evaluable dis

181 arboring CTNNB1 mutations have heterogeneous staining of beta-catenin and variable expression of gona

182 Cells with dual staining of both markers tended to be in well-to-moderat

183 Patients with higher dual-staining of CA19-9 and sTRA had statistically longer tim

184 ased expression of CTSB, as well as stronger staining of cathepsin B in the stratum granulosum of aff

185 of cell membranes, it controls the apparent staining of cells.

186 damage, as measured by the CometChip and the staining of DNA double-strand break marker, gammaH2AX.

187 and transmission electron microscopy and by staining of filamentous actin.

188 icroscopy of glomeruli and immunofluorescent staining of glomerular epithelial cells (podocytes) indi

189 y immunohistochemical and immunofluorescence staining of hearts and aortas.

190 sequent immunohistochemistry and fluorescent staining of histological features.

191 eth cell deficiency was assessed by lysozyme staining of ileum tissues and lysozyme activity in fecal

192 Haematoxylin and eosin staining of infarcts showed well demarcated zones of oed

193 errogans Histological periodic acid-Schiff D staining of infected kidney showed interstitial nephriti

194 d blood/tissue partitioning by intravascular staining of leukocytes, we showed that both inflammatory

195 Immunohistochemical staining of mice and human brain slices shows DAM with i

196 Immunohistological staining of occludin, Ki-67, NF-kappaB-p65, and terminal

197 Our exhaustive staining of paddlefish chromosomes combined with cytogen

198 Immunohistochemical staining of patient samples revealed that a significant

199 The cell imaging study revealed the staining of the cell and multicolor emission in the pres

200 i-DNAJB9 antibody showed strong and specific staining of the glomerular tufts in a distribution that

201 Immunohistochemical staining of the hippocampus detected nBMP2 in the nuclei

202 TJs of adjacent cells in immunofluorescence staining of the TJ molecules occludin and zonula occlude

203 In patients, immunohistochemical staining of tissue microarrays and mRNA expression analy

204 Selective detection and staining of toxic amyloid plaques, a potential biomarker

205 Immunofluorescence staining of ventral prostate tissue from obese HiMyc mic

206 ls to develop a reliable method for antibody staining of whole Drosophila larvae of any developmental

207 he method takes longer than typical antibody stains of dissected larval tissues-12 or 16 d, depending

208 Immunohistochemical staining on formalin-fixed BCCs from a dermatology clini

209 g was also validated with immunofluorescence staining on Foxp3(+)CD4(+) and PD-1(+)CD8(+) T cells.

210 in vivo was confirmed by immunofluorescence staining on multinucleated cells at the bone surface of

211 Furthermore, podoplanin staining on stromal cells was more diffuse, and CXCL12 s

212 t with classical hematoxylin and eosin (H&E) staining on the same tissue section.

213 owing Boolean Search String: "dye OR Lake OR Stain OR chromophore" AND "tox$ OR terato* OR carcino$ O

214 Without tissue staining or clearing, mPAM generates micrometer-resoluti

215 ub-micrometre level without the need for any staining or contrast agent.

216 erences were observed for phosphorylated tau staining or insoluble tau levels.

217 In contrast, cytoplasmic-restricted CASZ1 staining or low nuclear CASZ1 staining is found in tumor

218 with tear breakup time, corneal fluorescein staining, or ocular medications used by patients.

219 s with uveal melanoma with high nuclear BAP1 stain (P = 0.004).

220 tein 1, colocalize within a fingerprint-like staining pattern that correlates with ultrastructural mo

221 autoantibodies revealed a new sinusoidal C4d staining pattern when compared with HLA DSA (71% vs 3%;

222 As a conclusion, ACA displays a specific ANA staining pattern with a bimodal distribution, and ACA-po

223 combination with the MYC immunohistochemical staining patterns allows a more accurate prediction of p

224 gnificantly higher levels than the other ANA staining patterns in both RA and healthy population (p <

225 tructed fluorescent InsB10-23:DQ8 tetramers, stained peripheral blood lymphocytes directly ex vivo, a

226 xcision with comprehensive hematoxylin-eosin-stained permanent section margin control commonly known

227 se 4 separate PD-L1 antibodies on 2 separate staining platforms and have their own scoring systems, w

228 kin contains numerous epidermal patches that stain positive for p53 protein (p53 immunopositive patch

229 One-hundred fifty-one tumor specimens stained positive for podoplanin (33 high expression, 47

230 Diagnosis of MCC was confirmed by staining positive for cytokeratin 20 (CK20) and synaptop

231 barrier without harming the cell during the staining process.

232 ippocampal sections were processed for Nissl stain, Prox1-immunocytochemistry, GluR2-immunocytochemis

233 ) mice, a renal cystic model, ectopic p-Creb stained proximal tubule-derived cystic segments that los

234 panel, which are of major importance for the staining result.

235 on the retinal surface also showed positive stain results for type IV collagen.

236 with subsequently acquired immunofluorescent staining results.

237 Synaptophysin was used to stain retinoblastoma cells.

238 Congo red staining revealed brilliant red amyloid deposits confirm

239 3 cell types by means of immunofluorescence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis reve

240 e scored for TILs on hematoxylin-eosin (H&E)-stained sections, and immunohistochemical analysis was p

241 unted in tartrate-resistant acid phosphatase-stained sections.

242 Staining showed decreased fibrosis and improved angiogen

243 crescent formation, and nuclear phospho-p65 staining showed NF-kappaB activation within CD31-express

244 Ecocardiography and Masson staining showed that ZYZ-168 substantially improved card

245 The JC-1 staining shows the mitochondrial membrane potential is d

246 ferent biochemical conditions using negative stain single-particle EM.

247 CCT) and determined the failure rate of Gram stain smears (GSS) due to insufficient cellular material

248 Microscopic examination of acid-fast-stained sputum smears is the current standard of care in

249 onsidered pneumococcal if either sputum Gram stain, sputum culture, blood culture, or the immunochrom

250 d staining methods and developed a robust EV staining strategy, with the amine-reactive fluorescent l

251 IM1 antibodies on TRPC1-based SOCs and STIM1 staining suggest that channel activation may involve ins

252 ic of overlapping 3D stacks encompassing the stained surface.

253 the samples of choice for point-of-care Gram stain testing to diagnose Neisseria gonorrhoeae infectio

254 slight yet statistically significantly lower staining than either 28-8 or E1L3N, but this significanc

255 n exhibited a more prominent immuno-positive staining that correlated with rRNA transcription, as sho

256 ined within the dextran droplets and locally stain the tissue below with a contrast similar to the on

257 PCR-HRM analysis of DNA extracts from Giemsa-stained thick blood smears or corresponding blood pellet

258 re we examine young and aged primate retinae stained to distinguish S from M/L-cones.

259 abeling (TUNEL) and phospho-histone H3 (PH3) staining to assess apoptosis and cell proliferation, res

260 re examined first by hematoxylin-eosin (H&E) staining to establish the diagnosis of GCA.

261 We used hematoxylin-eosin staining to examine cochlear histopathological changes.

262 roscopy and fluorescence detection (Nile Red staining) to interrogate Mycobacterium tuberculosis cell

263 Here we use thioflavin T staining, transmission electron microscopy, as well as i

264 mortem human brains (7-46 years of age) were stained using a Golgi-Kopsch impregnation.

265 ization and target proteins are concurrently stained using immunofluorescence.

266 Double immunofluorescence staining using antibodies against choline-acetyltransfer

267 n stromal cells was more diffuse, and CXCL12 staining was dramatically reduced in Il-17ra(-/-) mice p

268 Wild-type TTR staining was less prominent in TTR-FAP patients.

269 OSM staining was observed in NPs, showed colocalization with

270 integrity, aurophosphate (Black Gold) myelin staining was performed on mPFC sections.

271 ith nuclear polarization, but exclusive sTRA staining was present in small clusters of cells with poo

272 Positive staining was present within the nerve fiber layer, inner

273 nce of macrophages, CD68 immunohistochemical staining was used.

274 d with diabetes, in combination with insulin staining, was performed to assess beta-cell selectivity

275 Using triple immunofluorescence staining we tested whether there were alterations in the

276 Using immunofluorescence staining, we confirmed the expression of ecto-5'-nucleot

277 with more than 10% and 1% nuclear tumor cell staining were considered, respectively, AR- and ER-posit

278 but histologic findings at hematoxylin-eosin staining were normal.

279 Hematoxylin and eosin and Oil Red O staining were performed to determine steatosis.

280 J mice, histochemical and immunocytochemical stains were performed for acetylcholinesterase (AChE), n

281 with COPD was assessed by immunofluorescence staining, Western blot analysis, and ELISA.

282 ipheral blood mononuclear cells samples were stained with a 38-marker immunophenotyping cytometry by

283 Sections were stained with anti-PGP9.5, anti-TTR, and Congo red.

284 Tissue was additionally stained with antibodies against gamma-aminobutyric acid

285 cellent concordance when scoring tumor cells stained with any antibody but poor concordance for scori

286 ut poor concordance for scoring immune cells stained with any antibody.

287 ield across images of several serial section stained with different protein markers.

288 Paraffin-embedded NP sections were stained with fluorescence-labeled specific antibodies ag

289 n fixed with formalin, embedded in paraffin, stained with hematoxylin and eosin, and/or fresh frozen.

290 ed in skin biopsy specimens from all lesions stained with hematoxylin-eosin and immunohistochemical m

291 Brain sections were histologically stained with Luxol Fast Blue (LFB) for myelin quantifica

292 ally had coarse collagen fibers and 24 of 26 stained with Miller elastic stain had decreased elastic

293 Both PCA and PN were stained with monoclonal anti-PSMA antibody (clone 3E6, 1

294 Staining with an antibody against M2FA demonstrated that

295 Immunofluorescence staining with anti-alpha-tubulin antibodies and cell cyc

296 fic B cells were identified using dual-color staining with fluorescently labeled PLA.

297 However, we found that staining with MitoTracker Green, a commonly used dye to

298 ls and sub-G1 populations as well as nuclear staining with orange fluorescence of treated cancer cell

299 g, cell surface cytokine-capture assays, and staining with peptide:MHC class II multimers, all of the

300 Finally, human AAA samples had stronger staining with the antibodies against 3-HAA, IDO, and kyn