ライフサイエンスコーパス: be assayed

1 lation in order that the correct populations are assayed.

2 y, and migration of eosinophils on periostin was assayed.

3 of this pathway in human autoimmune uveitis was assayed.

4 m different plant parts of Allium fistulosum were assayed.

5 ell as circulating measures of inflammation, were assayed.

6 responses of phytoplankton functional groups were assayed.

7 /PSA, SAX/PSA, Envi-Carb-II /SAX/PSA and C18 were assayed.

8 regulatory networks and biological functions were assayed.

9 ing mixes, extracts, and molecular allergens were assayed.

10 observed when combined antioxidant compounds were assayed.

11 John's Wort, sage, marjoram and thyme were assayed.

12 eurotrophic factors, and vascular parameters were assayed.

13 e and phenylethanolamine-N-methyltransferase were assayed.

14 nd the type of sorbent or extraction solvent were assayed.

15 eramidase protein and enzyme activity levels were assayed.

16 ctin, d-dimer, FVIII, and C-reactive protein were assayed.

17 outgrowth assays from resting CD4(+) T cells were assayed.

18 sized, and their in vitro binding affinities were assayed.

19 hydrolysates and fractions <10kDa and <3kDa were assayed.

20 W264.7 cells co-cultured with MC3T3-E1 cells were assayed.

21 n peripheral blood mononuclear cells (PBMCs) were assayed.

22 and Foxp3 methylation in MLN CD4(+) T cells were assayed.

23 metabolism, and markers of thyroid function were assayed.

24 vective drying (CDP) and ohmic heating (OHP) were assayed.

25 ents, UL34 bound to all predicted sites that were assayed (7 of 14).

26 HRMEC proliferation and tube formation were assayed according to standard protocols.

27 eritable loci will increase as the methylome is assayed across a broader range of cell types and the

28 Roux limb glucose consumption was assayed after surgery by positron emission and compu

29 ctivity of this new class of macrocycles has been assayed and analyzed.

30 erminal modifications of the native ProTx II was assayed and resulted in the identification of protox

31 Manual and in situ derivatization was assayed and the chromatographic response was higher

32 Localization of DSCAM was assayed and the protein was localized near to cone s

33 Further metabolism of the tested compounds was assayed and their transport modulated in an attempt

34 ad, IgG, and initial neutralization response were assayed and correlated with clinical and VAS inform

35 Trx and NADPH oxidase activities were assayed and NADPH oxidase isoforms, Nox2 and Nox4,

36 ay configurations, competitive and sandwich, were assayed and their performance for IgE determination

37 ks after finishing therapy, plasma Ab levels were assayed, and bone marrow was harvested.

38 Channel activity was assayed as ionic currents under patch clamp and as o

39 mycotoxin concentration in the raw materials were assayed as factors.

40 5 candidate 12-HETER1 promoter cis elements were assayed as luciferase reporter fusions in Chinese h

41 ry alpha-amylase and cortisol concentrations were assayed as neuroendocrine markers of stress respons

42 apause by a photoperiodic (short-day) signal were assayed as they traversed the diapause developmenta

43 okines by peripheral blood mononuclear cells was assayed, as were regulatory T-cell numbers and funct

44 he pathophysiology of THAP1 mutations should be assayed at multiple ages and neuronal types and suppo

45 cal advances have enabled DNA methylation to be assayed at single-cell resolution.

46 DPP-IV activity was assayed at 37 and 60 degrees C because cHSA solution

47 and 'Ser-129 phosphorylated alpha-synuclein' were assayed at 4-6 monthly intervals from a cohort of 1

48 Serum CRP levels were assayed at a central laboratory, and single-nucleot

49 ples from 27 pulmonary tuberculosis patients were assayed at diagnosis and during treatment.

50 as bentonite (B) and potassium caseinate (C) were assayed at different concentrations.

51 The products were assayed at increasingly low concentration, with the

52 a-smooth muscle actin-positive blood vessels were assayed at postoperative day 7 by colony formation

53 suppressed, chronically infected individuals were assayed at two time points separated by a 4- to 6-m

54 Furthermore, it can be assayed by DTI, potentially offering a quick, noninva

55 e range of proteins and interactors that can be assayed by hybrid-based approaches.

56 large amounts in fruits and vegetables, have been assayed by LC-MS/MS and derivatization chemistry us

57 Ascorbate was assayed by 2,6-dichlorophenolindophenol titration, a

58 The level of ROS generated was assayed by dihydroethidium.

59 lasma B lymphocyte stimulating factor (BLyS) was assayed by ELISA.

60 Endothelial progenitor cells (EPCs) was assayed by flow cytometer.

61 TF expression was assayed by functional and immunological assays.

62 Sb migration was assayed by HG-AFS for total determination and HPLC-I

63 Sb migration was assayed by ICP-MS and HG-AFS.

64 HPV16 E6 protein expression was assayed by immunohistochemistry in FCDIIB specimens

65 Ki-67 expression was assayed by immunohistochemistry.

66 Cell death was assayed by LDH and MTT methods.

67 easuring intracellular pH, and CFTR activity was assayed by measuring Cl(-) current.

68 Slc26a6 activity was assayed by measuring intracellular pH, and CFTR acti

69 the presence of B. burgdorferi DNA and mRNA was assayed by PCR and by real-time reverse transcriptio

70 HPV16 E6 DNA was assayed by polymerase chain reaction (PCR) and in si

71 Donor DNA was assayed by pyrosequencing for SP-D polymorphisms of

72 ified for each maternal-infant pair, and MMc was assayed by quantitative polymerase chain reaction.

73 CR) and in situ hybridization; HPV16 E6 mRNA was assayed by reverse transcriptase PCR.

74 Oxidative stress was assayed by single cell imaging of dihydroethidium.

75 e antioxidant capacity of the herbs extracts was assayed by spectrophotometric methods by using three

76 /loading of peptides in PLGA particles/films was assayed by two-phase extraction and amino acid analy

77 lications of the Au@MnO@SiO2 Janus particles were assayed by a cell viability analysis by coincubatin

78 Soluble Abeta oligomers were assayed by a single antibody sandwich enzyme-linked

79 Combinations of domain-coated beads were assayed by Bio-Plex technology as a high-throughput

80 Centromere size and location were assayed by chromatin immunoprecipitation for the hi

81 iadin antibodies of both IgG and IgA classes were assayed by ELISA in 44 non-celiac gluten sensitivit

82 lation of cocultured peripheral CD4+ T cells were assayed by ELISA.

83 Pre- and postinfection sera were assayed by enzyme-linked immunosorbent assay with N

84 Dynamics were assayed by fluorescence anisotropy of the fluoresce

85 Various types and lengths of mismatches were assayed by fluorimetry, and in many instances, our

86 Extracts were assayed by GC-FID, GC-MS, and LC-MS for the identif

87 and 16 pesticides whereas Cd, As, Pb and Hg were assayed by ICP-MS.

88 IRT3 and cleaved caspase-9 (CC-9) expression were assayed by immunoblotting with or without SIRT3 enf

89 Analyses of DC were assayed by liquid chromatography - tandem mass spec

90 Plasma specimens were assayed by liquid chromatography tandem mass spectr

91 Cytokines were assayed by means of ELISA.

92 esistant (HOMA-IR > 7, n = 9) obese subjects were assayed by microarray (Illumina HumanHT-12).

93 in vivo- and in vitro-cultured pollen tubes were assayed by microarray analyses, revealing over 500

94 dlings when apyrase expression is suppressed were assayed by microarray and quantitative real-time-PC

95 All mtDNAs were assayed by PCR-RFLP analysis and control region seq

96 Isolates were assayed by polymerase chain reaction for genes enco

97 ton samples (63-200 and > 200 mum fractions) were assayed by polymerase chain reaction for the preval

98 Saos-2 osteoblasts on new and treated disks were assayed by propidium iodide/DNA stain assay and con

99 a target gene, angiopoietin-like-4 (angptl4) were assayed by qRT-PCR.

100 Channel mRNAs were assayed by quantitative polymerase chain reaction.

101 nges in the expression of Stat5 target genes were assayed by quantitative real-time PCR assay.

102 genes in the TGF-beta signaling pathway and were assayed by quantitative RT-PCR for their associatio

103 Saliva swabs were assayed by real-time polymerase chain reaction for

104 TGF-beta inhibitor, and CTGF protein levels were assayed by Western blot analysis.

105 Three different temperature regimes were assayed (controlled, semi-controlled and non-contro

106 n groups of macromolecule-bound antioxidants were assayed: dietary fiber (DF), protein and lipid-boun

107 n an open-ended approach wherein an endpoint is assayed during or after the biological event of inter

108 Three measures of t-SP were assayed during reinstatement: dendritic spine morph

109 Barcoded proteins are assayed en masse in aqueous solution and subsequentl

110 trations of insulin, peptide YY, and ghrelin were assayed every 30 minutes.

111 ansposable elements from rice (Oryza sativa) are assayed for function in transgenic Arabidopsis thali

112 s only a few close relatives of sponges have been assayed for sterols.

113 lood was sampled postoperatively, and plasma was assayed for 25-OHD by liquid chromatography-tandem m

114 cripts were quantified by RT-PCR, and plasma was assayed for 3-OMG concentration.

115 removed to generate a 14-member library that was assayed for agonist activity at the mouse MC1R, MC3R

116 and the resulting sodium pertechnetate 99mTc was assayed for chemical, radiochemical, and radionuclid

117 (64)Cu-L19K-FDNB was assayed for covalent binding to VEGF in vitro.

118 Serum from infected ferrets was assayed for cross-reactivity to both seasonal and no

119 cHSA was assayed for DPP-IV activity using a specific DPP-IV

120 d from 75 type 2 diabetes regions, each gene was assayed for effects on multiple disease-relevant phe

121 Fetal plasma was assayed for insulin, testosterone and estradiol, pan

122 After imaging, the cartilage was assayed for its water, glycosaminoglycan, and collag

123 PfRH5-specific IgG was assayed for parasite growth-inhibitory activity.

124 Plasma was assayed for residual viremia (HIV-1 RNA) by qPCR.

125 The cell culture medium was assayed for the presence of the fluorescent signal u

126 household visits, children's drinking water was assayed for thermotolerant coliforms (TTC), an indic

127 The adduct (nDer p 2-Conj) was assayed for Toll-like receptor activation on transfe

128 All excised nodal packets (n = 36) were assayed for (99m)Tc activity, which established a l

129 105 asymptomatic healthy control individuals were assayed for 13 proteins relevant to cardiovascular

130 nts with surveillance or indication biopsies were assayed for 133 unique metabolites by quantitative

131 y treatment and before recurrence (n = 336), were assayed for 25(OH)D.

132 collected at 26 weeks' gestation or earlier were assayed for 25(OH)D.

133 Plasma obtained upon admission and over time were assayed for 26 inflammatory mediators and analyzed

134 ion With Initial Glargine Intervention trial were assayed for 284 biomarkers to identify those that c

135 Blood samples were assayed for 3-O-methylglucose to estimate glucose a

136 d and complemented and the resulting strains were assayed for acid survival.

137 The resulting compounds were assayed for antimicrobial activity against the ESKA

138 concentrates coming from aqueous treatments were assayed for antioxidant activity using the followin

139 s into hepatocytes whereby cell supernatants were assayed for ApoA-I.

140 of SPDEF were expressed in CRC cells; cells were assayed for beta-catenin activity and studied in im

141 Following standard pathology review, polyps were assayed for BRAF mutation (V600E) and tested for ML

142 lymphoblasts from 111 patients with BCP-ALL were assayed for CD22 expression and all were found to b

143 Cells were assayed for cell adhesion and cell motility and ana

144 ermeable filters treated for 5 days with GCs were assayed for changes in hydraulic conductivity.

145 intervention and at 4-month follow-up, which were assayed for circulating IL-6, a biomarker of system

146 These assemblies were assayed for contiguity, internal consistency, and a

147 Plasma and CSF collected pre-ART were assayed for cytokines and chemokines using a 17-ple

148 The cage hosts were assayed for dipeptide binding using competition ESI

149 participants with N348I at virologic failure were assayed for drug susceptibility.

150 om Escherichia coli or C. glutamicum mutants were assayed for efflux with different energy sources.

151 agnosed with prostate cancer, among whom 884 were assayed for ERG (426 ERG-positive).

152 Prerandomization sera were assayed for fatty acids among 641 men with incident

153 (n = 44) from low-income-households in Dhaka were assayed for fecal indicator bacteria (enterococci,

154 control subjects (n = 16 pairs, 32 samples) were assayed for genome-wide messenger RNA (mRNA) expres

155 Paired semen and blood samples were assayed for HCV RNA levels.

156 chool students who were born after July 1987 were assayed for hepatitis B surface antigen (HBsAg) and

157 Sera were assayed for IgE and gamma-tocotrienol levels.

158 trol subjects and patients with mastocytosis were assayed for IL-6, tryptase, and sIL-6R.

159 enantiomers and racemate of each metabolite were assayed for inhibition of the heat-shock response,

160 The plasma samples were assayed for insulin, glucose-dependent insulinotrop

161 after lipopolysaccharide-induced lung injury were assayed for leptin.

162 Both maternal and cord serum samples were assayed for levels of IgG1 and IgG3 specific for MS

163 ay for Campylobacter Stool and blood samples were assayed for markers of intestinal permeability and

164 PBMC from uveitis patients were assayed for MC5r expression on monocytes and A2Ar o

165 livary samples from 118 predialysis patients were assayed for MMP-8 by immunofluorometric assay.

166 isolated with laser-capture microdissection, were assayed for mtDNA deletions, copy number, and prese

167 mutated auxin responsive elements (AuxREs), were assayed for nematode-dependent gene expression.

168 Both were assayed for OM using immunohistochemistry (IHC) for

169 Plasma samples were assayed for P-tau (using an antibody that specifica

170 cus at baseline and 4 weekly visits after MC were assayed for pro-inflammatory cytokines and HIV RNA.

171 nally, single viable epithelial cells (which were assayed for PTP activity immediately after collecti

172 Tissue samples from participants were assayed for PTX3 levels using enzyme-linked immunos

173 n enantiomers of monomeric DKP ester insulin were assayed for receptor binding and in diabetic rats,

174 A set of these pleiotropic mutants were assayed for reduced toxicity in Drosophila melanoga

175 s of differentially abundant phloem proteins were assayed for SAR competence.

176 throughput genetics, 5560 minigene molecules were assayed for splicing in human HEK293 cells.

177 cipants the peripheral blood and nasal cells were assayed for T-cell activation and transcriptomic pr

178 ts displaying yellowing and inedible fruits, were assayed for the presence of phytoplasma DNA.

179 d and littermates negative for the transgene were assayed for the presence of serum phosphorylated ne

180 were overexpressed in the Col background and were assayed for their ability to delay flowering.

181 CCT5 complexes were assayed for their ability to suppress aggregation o

182 synthesized molecules, as a racemic mixture, were assayed for their EcDXR inhibitory potency.

183 asmodium falciparum DHODH, all the compounds were assayed for their effect on P. falciparum growth.

184 enty-eight Y chromosomes of worldwide origin were assayed for their resistance to the X-linked sex-ra

185 nse against this toxin, the two CPB variants were assayed for their trypsin sensitivity.

186 The samples were assayed for total antioxidant capacity and SOD acti

187 obtained during 7-12 years of effective ART were assayed for total HIV-1 DNA and 2-long terminal rep

188 The blood samples were assayed for total mercury using inductively coupled

189 panese cultivars, Yabukita and Yutakamidori, were assayed for total polyphenols (TP) content, individ

190 nts with surveillance or indication biopsies were assayed for urinary CXCL10 using enzyme-linked immu

191 If antibodies developed, proximate samples were assayed for viral load by polymerase chain reaction

192 rospectively observed patients with melanoma were assayed for vitamin D and CRP.

193 de that occurred in Long Island, NY, in 2009 were assayed for XUV and PTA3 expression and compared wi

194 Interleukin-6 abundance could be assayed from concentrations as low as 50 pM (an order

195 RTL was assayed from blood or saliva samples.

196 Over 500 million CD4+ T cells were assayed from both participants in a humanized mouse

197 osterone, and cotinine (nicotine metabolite) were assayed from third trimester maternal sera.

198 mentalized in water-in-oil emulsion droplets are assayed, has emerged as a powerful format for direct

199 Peptides are assayed in a 96-well dot blot apparatus using membra

200 When several genes are assayed in parallel these effects can be estimated a

201 icates of 15 samples (i.e., 120 analyses) to be assayed in <120 min.

202 The biosensor cells can be assayed in a high throughput, noninvasive manner, wit

203 tly, both of these locomotion phenotypes can be assayed in an automated manner suitable for high-thro

204 d the transcriptomes of hundreds of cells to be assayed in an unbiased manner, opening up the possibi

205 Up to 2,000 cells can be assayed in one experiment at a rate of 6 s per cell.

206 atio) overcomes this limitation but has only been assayed in small cohorts.

207 Solubilization has been assayed in the 4-50 degrees C range, and the result

208 tion in copy number (CNV) of specific HvCBFs was assayed in a panel of 41 barley genotypes using RT-q

209 is (Arabidopsis thaliana) stem wax secretion was assayed in a series of vesicle-trafficking mutants,

210 Mitochondrial H2O2 production was assayed in arterioles using mito peroxy yellow 1.

211 Concurrent serum cystatin C was assayed in banked serum samples.

212 Binding specificity was assayed in CD-1 and sEH knock-out mice and Papio anu

213 thylation at approximately 470,000 CpG sites was assayed in CD4(+) T cells using the Illumina Infiniu

214 Collagen content was assayed in cell culture supernatant.

215 BPA was assayed in first-trimester urine samples from 385 pa

216 -specific transcription factor binding sites was assayed in mice and in HepG2 cells.

217 In vitro, caspase activity was assayed in Per1/2-specific small interfering RNA-tra

218 Diagnostic performance was assayed in simple broth-enriched blood samples and s

219 acylation on the prion-like seeding of SOD1 was assayed in spinal cord extracts of transgenic mice e

220 rase activity with locomotor activity, which was assayed in the same flies with video recording.

221 Transport function of the mutants was assayed in transient transfectants by measurement of

222 essed in bacteria, and polyP kinase activity was assayed in vitro.

223 sinophil-lineage-committed progenitors (EoP) were assayed in 21 severe eosinophilic asthmatics, 19 mi

224 anganese, molybdenum, nickel, lead and zinc) were assayed in a cohort of 949 individuals using mass s

225 Serum levels of insulin, leptin, and ghrelin were assayed in all 104 fasting men with Barrett's esoph

226 transmitter mothers, and 47 infected infants were assayed in an HIV-1-inducible green fluorescent pro

227 ated rejection (AMR) + and 15 who were AMR-, were assayed in C1q-binding assays (C1q Screen; One Lamb

228 spot mutations in ESR1 and PIK3CA from ctDNA were assayed in clinical trial samples from ER+ metastat

229 Isolated proteins were assayed in ELISA and ELISA inhibition, basophil act

230 Factor XIII-A transcripts were assayed in human umbilical blood haemopoietic cell

231 e N3, N-Acetyl-L-Cysteine and Pluronic F-68) were assayed in order to improve production yields in a

232 The activities of the naphthyridinols were assayed in phosphatidylcholine unilamellar liposome

233 Biomarkers were assayed in plasma samples obtained from 341 subject

234 , GTPCH1 ubiquitination, and GTPCH1 activity were assayed in purified GTPCH1, endothelial cells, and

235 ycolytic flux and mitochondrial respiration, were assayed in real time for a panel of wild-type (wt)

236 Enantiomers of 2-methylbutyl acetate were assayed in red and white commercial wines from vari

237 Fifteen anionophores were assayed in single cells by monitoring anion transpo

238 Levels of MYOM3 fragments were assayed in therapeutic model systems: (1) restorati

239 Smooth-muscle cells from mouse tracheas were assayed in vitro for signaling pathways.

240 al trial patients with matched clinical data were assayed in vitro to determine murine macrophage upt

241 and replication capacities of these mutants were assayed in vitro.

242 Extractable MXE and XET activities were assayed in vitro.

243 d hits in the screen (first step) then could be assayed individually for inhibition of binding of liv

244 .45, respectively) and germline variants can be assayed noninvasively, our findings provide potential

245 commonly excluded from GWAS analyses despite being assayed on all current GWAS microarray platforms.

246 itionally, restriction endonuclease activity is assayed on simple substrates such as plasmids and syn

247 Phosphoglucomutase 1 enzyme activity was assayed on cell extracts.

248 ian cancer, fresh frozen tumor DNA (n = 485) was assayed on Illumina Infinium HumanMethylation450 Bea

249 Cytosine-phosphate-guanine (CpG) methylation was assayed on the HumanMethylation450k microarray, and

250 CpG methylation in isolated B lymphocytes was assayed on the Illumina HumanMethylation450 BeadChip

251 Cell proliferation was assayed over time, and migration was evaluated by Li

252 The method allows for more samples to be assayed per unit time, it uses less solvent than othe

253 Three different approaches were assayed: pre-incubation of bacteria and compounds b

254 idence for inference and therefore could not be assayed precisely by TREDPARSE.

255 in, and growth and differentiation factor-15 were assayed preoperatively and over the first week post

256 on with tetramethylammonium hydroxide (TMAH) was assayed prior to inductively coupled plasma mass spe

257 tome-wide m(6)A patterns in Arabidopsis have been assayed recently.

258 icroreactor, allowing multiple substrates to be assayed simultaneously.

259 t experiment, only limited number of samples were assayed, thus the classical 'large p, small n' prob

260 Three of the most used hydrolases were assayed to catalyze the process, and beta-glucosida

261 ion, gene expression, and protein expression were assayed to explore the effects of these inhibitors

262 chicken skin, porcine limb, and bovine liver were assayed to investigate the effect of anatomical het

263 holipid secretion and taurocholate transport were assayed to investigate the effect of selected drugs

264 This approach allows TREs to be assayed together with gene expression levels and othe

265 ssays by our device, a total of 1030 samples are assayed using three immunoassay methods to detect si

266 al model for toxicity and animal disease can be assayed using an electrochemical approach.

267 -translational regulatory mechanism that can be assayed using high-throughput mass spectrometry (MS).

268 pt levels from all nine csp genes have never been assayed using the same technique or in the same cel

269 Intracellular reactive species content was assayed using 2',7'-dichlorofluorescein diacetate dy

270 Salivary total alpha-synuclein was assayed using a highly sensitive Luminex assay and o

271 Function was assayed using dual cell two-electrode voltage clamp

272 Global gene expression was assayed using human microarray chips.

273 anic acids in the examined pumpkin cultivars was assayed using the method of high performance liquid

274 ermined using HPLC, and antioxidant activity was assayed using the TEAC system based on the 2,2'-azin

275 ids as standards for 16S rRNA gene estimates was assayed using these two prokaryotic systems, with th

276 anges in the gA monomer<-->dimer equilibrium were assayed using a gA channel-permeable fluorescence q

277 IL-6 levels were assayed using an enzyme linked immunosorbent assay

278 GCR and mercuric reductase activities were assayed using enzyme that was expressed in Escheric

279 Glucose transport and consumption were assayed using ex vivo jejunal loops.

280 ygen species levels and mitochondrial stress were assayed using fluorogenic probes, microscopy, and f

281 Functional differences in secreted VEGF were assayed using HUVEC migration.

282 linic patients who underwent cardiac surgery were assayed using Illumina Human HT-12 mRNA microarrays

283 baseline and after 12 months of peanut SLIT were assayed using ImmunoCAP for IgE and IgG4 against wh

284 , Wales, and Northern Ireland during 2014-15 were assayed using MATS and compared with 2007-08 data.

285 lume plasma samples (>20 ml) from 7 patients were assayed using Mega-iSCA, and HIV-1 RNA was quantifi

286 ve patch-test sites from non-atopic patients were assayed using quantitative PCR and immunohistochemi

287 g (20-24 years) and old (54-70 years) donors were assayed using ribonucleic acid sequencing (RNA-seq)

288 to ozone or short-fragment HA (sHA), and AHR was assayed via flexiVent.

289 rns were determined and functional diversity was assayed via measurements of potential enzyme activit

290 DNA from brain and blood tissue was assayed via the Illumina Infinium Methylation 450 K

291 ues were mutated to alanine, and kcat and Km were assayed whenever kinase and/or cyclase activity was

292 Survival of mammalian cells was assayed with good result.

293 ThDP was assayed with great sensitivity (3831mAM(-1)cm(-2)) o

294 rtichoke (Cynara scolymus L.) flower extract was assayed with the aim of replacing animal rennet in t

295 The anti-mutagenic properties was assayed with the following HCAs: 2-amino-3-methylimi

296 Primary tumors were assayed with a validated gene expression assay that

297 vors of B. tabaci infected by I. fumosorosea were assayed with I. fumosorosea.

298 All compounds were assayed with nNOS, their IC50, KI, and kinact value

299 the second year of antiretroviral treatment were assayed with three FDA-approved platforms: UltraSen

300 Splenocytes from VACV-WR-infected mice were assayed without prior expansion against the soluble