ライフサイエンスコーパス: ELISA

1 ELISA analyses showed that inhalation of hydrogen-oxygen

2 ELISA and bio-layer interferometry measurements demonstr

3 ELISA assay revealed the PEG-GCSF had the longest plasma

4 ELISA using polyclonal anti-HCP antibodies as reagents f

5 ELISA was used to assess the production of IgE, type 2 c

6 d named Top 3-ID-DIA was benchmarked against ELISA and a gold-standard selected reaction monitoring a

7 ination of MC-LR was cross validated against ELISA.

8 fferences between the proposed method and an ELISA method in AFP and CA125 measurements of serum samp

9 eron gamma (IFNG), which is quantified by an ELISA.

10 by 10, was used successfully to construct an ELISA-based assay where 2 and 10 serve as the capture an

11 We developed an ELISA and multiplex assay to model the cross-linking of

12 SELEX protocol, and their application in an ELISA assay for sensitive diagnosis of Zika NS1 protein.

13 ties of two monoclonal antibodies used in an ELISA for the quantification of the major birch pollen a

14 When used in an ELISA format, the aptamer displays both high precision (

15 AT1R-Ab was measured on an ELISA platform.

16 Running an ELISA involves adding sample (e.g. blood) and water, mov

17 in blood, tissue, and cell cultures using an ELISA.

18 le agreement with the those obtained with an ELISA assay as reference method.

19 ion and neuron loss versus myelin alone, and ELISA experiments revealed that myelin serine proteases

20 escence staining, Western blot analysis, and ELISA.

21 of the DNA/AuNPs for colorimetric assays and ELISA feasibility; additionally, SPR imaging analysis of

22 Dot blot and ELISA assays demonstrate the inhibition of the putative

23 expression was confirmed by Western blot and ELISA, and OPN was purified using Ni affinity chromatogr

24 ontent were quantified by flow cytometry and ELISA, respectively.

25 ls were analyzed by using flow cytometry and ELISA.

26 nd control subjects using flow cytometry and ELISA.

27 lin (BGG) was assessed by immunoblotting and ELISA, respectively.

28 Immunoprecipitation and ELISA-style binding assays confirmed a direct interactio

29 e secretion was measured using multiplex and ELISA.

30 Real-time PCR and ELISA analyses showed that ER stress induced a pro-infla

31 re assessed by using quantitative RT-PCR and ELISA and a multiplex kit for IL-35 and IL-12, respectiv

32 PCR and ELISA could in principle be used for this purpose.

33 Quantitative RT-PCR and ELISA were used to determine transcript and secreted cyt

34 ne levels by performing quantitative PCR and ELISA.

35 Gene array, real-time PCR, and ELISA analyses showed that treatment of endothelial cell

36 ression changes were verified by RT-qPCR and ELISA.

37 METHODS AND Mass spectrometry and ELISA assays detected significant accumulation of LXA4 i

38 EIA determined leukotriene B4, and ELISAs quantified TNF, IL-12 and IL-10 in the gingival t

39 cteristic curves to show that serum antibody ELISA, copro-antigen ELISA and faecal egg counting can b

40 how that serum antibody ELISA, copro-antigen ELISA and faecal egg counting can be useful in distingui

41 ed to Toxocara excretory - secretory antigen ELISA (TES - ELISA).

42 were defined by using chemotaxis, apoptosis, ELISA, Luminex, quantitative RT-PCR, and flow cytometric

43 sed by an enzyme-linked immunosorbent assay (ELISA) against the glycoprotein of the ZEBOV-Kikwit stra

44 say, (ii) enzyme-linked immunosorbent assay (ELISA) and (iii) in-vivo co-expression and screening in

45 hrough an enzyme-linked immunosorbent assay (ELISA) and a histo-blood group antigen (HBGA) blocking a

46 ercial GM enzyme-linked immunosorbent assay (ELISA) and a PCR assay based on amplification of the pan

47 antibody enzyme-linked immunosorbent assay (ELISA) and fluke egg counts.

48 those of enzyme-linked immunosorbent assay (ELISA) and other immunoassay methods.

49 AR by the enzyme-linked immunosorbent assay (ELISA) assay.

50 ed by the enzyme-linked immunosorbent assay (ELISA) conventional method (p-value of < 0.05) showed th

51 ext of an enzyme-linked immunosorbent assay (ELISA) for HBeAg quantification, which we compared with

52 sandwich enzyme-linked immunosorbent assay (ELISA) for PEG by tethering an anti-PEG antibody (AGP3)

53 g a novel enzyme-linked immunosorbent assay (ELISA) format as a screening assay, we found that a hydr

54 d through enzyme linked immunosorbent assay (ELISA) in saliva samples of oral cancer patients.

55 sponse in enzyme-linked immunosorbent assay (ELISA) in terms of sensitivity and reproducibility and w

56 Enzyme-linked immunosorbent assay (ELISA) is one of the most important technologies for bio

57 Enzyme-linked immunosorbent assay (ELISA) measurements of the supernatants of the sorted hy

58 Enzyme-linked immunosorbent assay (ELISA) performed on supernatant fluids of LPS challenged

59 using an enzyme-linked immunosorbent assay (ELISA) technique with a regression value of 0.9951.

60 llowed by enzyme-linked immunosorbent assay (ELISA) validation.

61 rofluidic enzyme-linked immunosorbent assay (ELISA) was developed as a screening system for rapid det

62 ntitative Enzyme-Linked ImmunoSorbent Assay (ELISA) was formatted to assess relative immunoreactivity

63 the rapid enzyme-linked immunosorbent assay (ELISA) was more variable and dependent on the polymorphi

64 tary body enzyme-linked immunosorbent assay (ELISA) was used to investigate serum anti-CT immunoglobu

65 ection by enzyme-linked immunosorbent assay (ELISA), and cBIN1 level decreased in humans with heart f

66 multiplex enzyme-linked immunosorbent assay (ELISA), and the microbiota by 16S ribosomal ribonucleic

67 ecificity enzyme-linked immunosorbent assay (ELISA), and the second-tier tests are higher-specificity

68 Enzyme-linked immunosorbent assay (ELISA), flow cytometry, and Western blot are common bioa

69 validated enzyme-linked immunosorbent assay (ELISA), resulting in excellent Pearson correlation and i

70 Using enzyme-linked immunosorbent assay (ELISA), we obtain seropositivity of 77%.

71 using an enzyme-linked immunosorbent assay (ELISA)-type binding assay.

72 tter than enzyme-linked immunosorbent assay (ELISA).

73 okines by enzyme-linked immunosorbent assay (ELISA).

74 one-step enzyme-linked immunosorbent assay (ELISA).

75 e-analyte enzyme-linked immunosorbent assay (ELISA).

76 asured by enzyme-linked immunosorbent assay (ELISA).

77 ting, and enzyme-linked immunosorbent assay (ELISA).

78 gcBIOMICS enzyme-linked immunosorbent assay (ELISA).

79 onduct an enzyme-linked immunosorbent assay (ELISA).

80 been the enzyme-linked immunosorbent assay (ELISA); however, newer technologies are emerging with in

81 histochemistry, the Luminex Multiplex assay, ELISA, PCR, and immunoblotting and linked to the presenc

82 s, including fluorescence, enzymatic assays (ELISA), and quantitative real-time PCR.

83 include enzyme-linked immunosorbent assays (ELISA) and direct tissue blot immunoassays (DTBIA).

84 ified by enzyme-linked immunosorbent assays (ELISA) or theoretically calculated in 12 brain regions,

85 tion and enzyme-linked immunosorbent assays (ELISA) which tested serological HBV markers were applied

86 such as enzyme-linked immunosorbent assays (ELISA), Western blot, high performance liquid chromatogr

87 both in enzyme-linked immunosorbent assays (ELISA).

88 Enzyme-linked immunosorbent assays (ELISAs) based on ZIKV and DENV nonstructural protein 1 (

89 ifferent enzyme-linked immunosorbent assays (ELISAs) for gluten detection each have specific characte

90 lassical enzyme-linked immunosorbent assays (ELISAs) in the quantification of HIV-1 Gag p24 productio

91 petition enzyme-linked immunosorbent assays (ELISAs) showed that antisera from immunized mice inhibit

92 HLA antibodies detected in the ECXM and AT1R ELISA and microvascular injury observed in antibody medi

93 e and point-of-care device for the automated ELISA.

94 ing the results using commercially available ELISA kit for CXCL5 detection.

95 were analyzed using multianalyte bead-based ELISA assays.

96 CS analysis and a newly developed cell-based ELISA.

97 are comparable to standard laboratory-based ELISA in whole blood.

98 present a conceptually novel reaction-based ELISA principle (ReactELISA) for quantitation of the car

99 d is often accomplished using antibody-based ELISAs.

100 uggest that the developed MAb based dot blot ELISA is a simple, rapid performed in less than 8 h, ine

101 ded for the evaluation of MAb-based dot blot ELISA.

102 assays including amyloid kinetics, dot blot, ELISA, and TEM show that 5 effectively inhibits both Abe

103 We used qRT-PCR, Western blotting, ELISA, and ChIP (chromatin immunoprecipitation) to chara

104 By ELISA, two analytes (ST2 and Spondin-1) best described l

105 the production of cytokines was analyzed by ELISA or intracellular staining and flow cytometry, and

106 cts were measured using SDS-PAGE gels and by ELISA whereas Amadori products were assessed by the fruc

107 try, and soluble mediators and antibodies by ELISA; the percentage of migratory CD1a(+) dermal DCs wa

108 tyrosine and 4-hydrpxnonenal both assayed by ELISA, insulin secretion quantified using ELISA or radio

109 IgG responses in C57BL/6 mice as assayed by ELISA.

110 that received 3 million PFU, as assessed by ELISA and by pseudovirion neutralization assay.

111 mmatory cells and cytokines were assessed by ELISA.

112 th and without meat allergy were assessed by ELISA.

113 osis factor-alpha (TNFalpha) was assessed by ELISA.

114 icosteroids in both cohorts were compared by ELISA, immunoblot, immunohistochemistry and real-time PC

115 nding of IgE and IgG to BGG was confirmed by ELISA and completely abolished after pre-incubation with

116 This was confirmed by ELISA-based analysis of the TREM2-TYROBP interaction.

117 ITMS/MS, but could not always be detected by ELISA.

118 blood serum as well as for its detection by ELISA, Western blot, flow cytometry, and confocal micros

119 onable relationship between CM determined by ELISA and HPLC-ESI-ITMS/MS and therefore supports the im

120 tokine/protein signatures were determined by ELISA, cytometric bead array, or quantitative PCR.

121 /- 30.6 ng/mL] (P = 0.014), as determined by ELISA.

122 IgE binding was determined by ELISA.

123 ifferent human neurodegenerative diseases by ELISA, immunohistochemistry and immunoblots.

124 IgG4 were established by ELISA in 2 cohorts: parents born 1945-1972 (n = 171) and

125 the IL1RL1 distal promoter were examined by ELISA and PCR sequencing in UC patients receiving cortic

126 4 serum samples were tested for both GPC3 by ELISA, and AFP by immunometric assay.

127 parum was determined in 4,112 individuals by ELISA using eluted dried blood from filter paper.

128 city in sensitized mice were investigated by ELISA, rat basophil leukemia assay, T-cell proliferation

129 Moreover, we measured cortisol levels by ELISA and found that mevastatin inhibited cortisol synth

130 e determined serum IgA and gd-IgA1 levels by ELISA in a sample of 148 healthy female twins, including

131 d histamine production in response to LPS by ELISA.

132 IL-17F protein was also measured by ELISA in bronchial/nasal lysates and by immunohistochemi

133 ' IgE for binding to Bet v 1 was measured by ELISA inhibition.

134 Circulating BMP-9 levels were measured by ELISA.

135 Serum levels were measured by ELISA.

136 -1) levels in culture media were measured by ELISA.

137 tants of PLA-specific cells were measured by ELISA.

138 While HCP are usually monitored by ELISA, mass spectrometry (MS)-based approaches are emerg

139 l flow cytometry and measured nephrinuria by ELISA.

140 lts highly correlated with those obtained by ELISA performed with monoclonal CML-antibody (beta=0.98,

141 f antibodies against the Ct antigen Pgp3, by ELISA.

142 ns properly, that were essentially proven by ELISA.

143 nd thromboxane B2 (TXB2 ) were quantified by ELISA, and PGF2alpha (FP) and thromboxane A2 (TP) recept

144 CCL-18 and CCL-20 levels were quantitated by ELISA in BALF and serum samples from 60 LTRs.

145 was measured in the culture supernatants by ELISA.

146 Validation by ELISA confirmed that compared with controls, cases had s

147 Whole-cell ELISA was used to establish the surface staining of CR-K

148 uman primates which survived EBOV challenge, ELISA, western blot, mass spectrometry and flow cytometr

149 ed every two weeks and analysed by CN54gp140 ELISA and antigen-specific B cells were measured by flow

150 d enhancement over conventional colorimetric ELISA.

151 ction ( 10 pg/mL) over standard colorimetric ELISA methods.

152 Commercial ELISA kits are known to give false-positive results for

153 nt with those obtained by using a commercial ELISA kit.

154 during extraction of OTA using a commercial ELISA protocol.

155 M measurements were determined by commercial ELISA (LISA TRACKER, Theradiag, France).

156 out ten times more sensitive than commercial ELISAs, and covers a dynamic range of three orders of ma

157 el of 279 human sera from the CDC, comparing ELISAs using these two recombinant antigens with the 2-t

158 we used to develop an NS1-based competition ELISA.

159 We describe a highly sensitive competition ELISA to measure integrin-binding of RGD-peptides in hig

160 mparison to the state-of-the-art competitive ELISA for their higher affinity towards target analytes.

161 te Diversity Set II and in vitro competitive ELISA we have identified three compounds (NSC201631, NSC

162 This assay adapts a conventional ELISA format with immobilized RalGDS-RBD as a bait to se

163 lts also correlated well with a conventional ELISA PRA assay, with a coefficient of determination of

164 eutical HCP profiling alongside conventional ELISA, because individual species can be identified and

165 ng) with good correlation with conventional ELISA method (Pearson's r = 0.987).

166 eric alphaSyn species in AD brains by custom ELISA, size-exclusion chromatography, and nondenaturing/

167 Activation was measured by flow cytometry, ELISA of cultured supernatants, and F-actin staining; ap

168 tion were evaluated by using flow cytometry, ELISA, and histology.

169 were determined by means of flow cytometry, ELISA, and multiplex immunoassay.

170 ys were assessed by means of flow cytometry, ELISA, Luminex, and immunohistochemistry.

171 ro diagnostic assays during the last decade, ELISAs have become a workhorse in routine clinical diagn

172 This work compares three different ELISA assays and HPLC-ESI-ITMS/MS for the analysis of CM

173 immunoassays were developed using different ELISA formats.

174 d more expensive, approaches such as digital ELISA.

175 IFNalpha attomolar concentrations by digital ELISA will enhance our understanding of IFN biology and

176 Using single-molecule array (Simoa) digital ELISA technology, we recorded attomolar concentrations o

177 t study, we report an ultrasensitive digital ELISA platform for quantification of the HIV-1 protein p

178 nterferon alpha protein levels using digital ELISA, enhanced interferon signaling by RNA-Seq analysis

179 Our FcgammaR dimer ELISA readily detected Abs in samples from two separate

180 rium-related protein, which was selected for ELISA validation.

181 new miniature mobile phone based system for ELISA (MELISA).

182 We analyzed longitudinal IFN-gamma, ELISA-antibody and fecal shedding experimental sensitivi

183 sion and illustrates that Th1/Th2 (IFN-gamma/ELISA antibodies) assays are important for infection det

184 amines the feasibility of harmonizing gluten ELISA assays by the introduction of: a common extraction

185 raphy, immunohistochemical staining, and HGF ELISA assays confirmed that elevated levels of HGF prote

186 hy and immunohistochemistry, and ex vivo HGF ELISA experiments were performed on murine xenografts of

187 IgE-western blot and IgE-ELISA were complemented by Skin Prick Testing (SPT) and

188 competitive assay or on an indirect EBOV IgG ELISA.

189 y titres were dose-related (p=0.0003 for IgG ELISA and p<0.0001 for the 60% plaque-reduction neutrali

190 e 2 x 10(7) PFU dose, the geometric mean IgG ELISA endpoint titre was 1624 (95% CI 1146-2302) and ser

191 Addition of DENV1-NS1 IgG ELISA can distinguish primary ZIKV infection; the ratio

192 o of absorbance of ZIKV-NS1 to DENV1-NS1 IgG ELISA can distinguish ZIKV with previous DENV and second

193 oglobulin M (IgM) and immunoglobulin G (IgG) ELISAs combined can detect ZIKV infection with a sensiti

194 detection of IgM antibodies with capture-IgM ELISA.

195 ELISA, and the Euroimmun anti-Zika Virus IgM ELISA.

196 articles was demonstrated in an immunoassay (ELISA) format in buffer and complex media (milk or blood

197 their sIgE reactivity assessed by ImmunoCAP, ELISA, cross-inhibition, and basophil activation test (B

198 Using western blotting, immunofluorescence, ELISA and qRT-PCR, we investigated the production of tra

199 acillin-BSA adduct was used as an antigen in ELISA antibody binding studies.

200 However, the strongest IgE binding in ELISA was noted against APE.

201 or reporter protein fusions are evaluated in ELISA, flow cytometry, and Western blot experiments and

202 the biotinylated nanobody A2.3 performed in ELISA with excellent recovery and high sensitivity, IC50

203 peanuts perturbed allergen quantification in ELISAs, probably via exposure of additional epitopes.

204 IgE binding was tested in inhibition ELISAs and basophil activation tests.

205 Incorporating PVPP into ELISA protocols allows for the continued use of rapid im

206 pture enzyme-linked immunosorbent assay (MAC-ELISA) followed by supplemental testing of specimens wit

207 pture enzyme-linked immunosorbent assay (MAC-ELISA) for screening, followed by a confirmatory plaque

208 ) Zika MAC-ELISA, the InBios ZIKV Detect MAC-ELISA, and the Euroimmun anti-Zika Virus IgM ELISA.

209 isease Control and Prevention (CDC) Zika MAC-ELISA, the InBios ZIKV Detect MAC-ELISA, and the Euroimm

210 n ZIKV ELISA to either the CDC or InBios MAC-ELISAs resulted in positive agreement, negative agreemen

211 sequently quantified the EVs via a microchip ELISA.

212 Multiplex ELISA measured BAL cytokines.

213 nes the simplicity and cost-effectiveness of ELISA with the sensitivity and speed of modern approache

214 and therefore supports the implementation of ELISA in food CML/AGEs screening.

215 inity for specific SAEs, assayed by means of ELISA and surface plasmon resonance, were recloned as Ig

216 PCR in the liver and spleen and by means of ELISA in plasma.

217 ed for basement membrane binding by means of ELISA.

218 ed IL-1beta levels were measured by means of ELISA.

219 ll be helpful for appropriate calibration of ELISAs.

220 th Stx2 binding to the Gb3 receptor based on ELISA results, underlining the POS anti-STEC properties.

221 EIA alone or in combination with CCNA and/or ELISA as the reference method, the accuracy of CT was me

222 eported with other previous immunosensors or ELISA kits.

223 Compared to PCR- or ELISA-based methods, this assay enables separate quantit

224 ology, immunohistochemistry, immunoblots, or ELISAs (to measure cytokines).

225 However, the DbpA/C6-OspC ELISA was markedly better (80% versus 63%) than the 2-ti

226 , immunohistochemistry, quantitative RT-PCR, ELISA, and flow cytometry.

227 The library was panned and screened by phage ELISA using trimeric recombinant proteins to identify vi

228 ed and screened for peptide binding by phage ELISA.

229 In solid phase ELISA-based ligand binding assays, purified pentameric H

230 inflammatory factors were measured by qPCR, ELISA, and Western blotting.

231 Quantitative ELISA showed no evidence of decreasing AmCYAN1 and PMI p

232 method of the Bet v 1-specific quantitative ELISA adopted by the European Pharmacopoeia.

233 Using R-Biopharm R5 ELISA, we quantified gluten in gluten-free oatmeal servi

234 y publications have highlighted that routine ELISA methods do not give rise to equivalent gluten cont

235 volume of reagents, and time required to run ELISA for food sample testing.

236 Sandwich ELISA assays revealed significantly reduced soluble Abet

237 Based on a sandwich ELISA and the specific recognition of antibody to E. col

238 iable-length tethers for cell-based sandwich ELISA, therefore, provides a sensitive, high-capacity me

239 harvested after light exposure for sandwich ELISA-based assays to quantify 10 pro-angiogenic cytokin

240 is a versatile tool for generating sandwich ELISA-grade and bispecific reagents.

241 R-Biopharm R5 sandwich ELISA R7001 is used for analysis of all the first15-g po

242 In analyses of 500 sera, ELISA using rLb6H detected all 219 ATL samples (sensitiv

243 thm for ZIKV serodiagnosis based on 3 simple ELISAs is proposed to distinguish primary ZIKV, ZIKV wit

244 ects were used in an IgE-anti-IL-24-specific ELISA to investigate the association of IgE-anti-IL-24 a

245 lasma levels were determined with a specific ELISA.

246 on molecular and cellular levels using SPR, ELISA, and flow cytometry.

247 -quality monoclonal antibodies in a standard ELISA detection assay.

248 ell with the values obtained from a standard ELISA.

249 of the biosensor were compared with standard ELISA and multiplex DVD-array high-throughput screening

250 a excretory - secretory antigen ELISA (TES - ELISA).

251 TF ELISA, soluble P-selectin, d-dimer, FVIII, and C-reactiv

252 o washes, includes fewer hands-on steps than ELISA, while also achieving superior sensitivity.

253 oach was found to be 1,000 folds higher than ELISAs (10(2)cellsmL(-1)).

254 The ELISA is the mainstay for sensitive and quantitative det

255 The ELISA responses showed high variability depending on the

256 erved limited cross-immune reactivity by the ELISA but little reactivity by the HBGA blocking assay b

257 m is a viable diagnostic replacement for the ELISA for viral hemorrhagic fevers.

258 Compared to the ELISA method, our system requires less analysis time (</

259 Using the ELISA results, statistical analyses using nonparametric

260 he obtained results correlated well with the ELISA used in the clinic for assaying glucose-stimulated

261 red the performance characteristics of three ELISAs for the detection of IgM class antibodies to ZIKV

262 ration of study targets was assessed through ELISA and the ratio of serum TGF-beta1/ENG (T/E) was eva

263 uPAR levels were determined in serum through ELISA in UK (cases n = 129; controls n = 39) and Dutch (

264 se antigens could be used in a simple 1-tier ELISA that is faster to perform, easier to interpret, an

265 ts and superior sensitivity when compared to ELISA based techniques.

266 lable kits have been observed with regard to ELISA and PCR methods.

267 mpare the MagPix platform with a traditional ELISA for IgM and antigen detection of infections from L

268 tection platforms range from the widely used ELISA to more sophisticated, and more expensive, approac

269 Using ELISA, we confirmed the presence of various amounts of c

270 Sera were assessed for autoantibodies using ELISA assays.

271 or anti-FB and anti-C3b autoantibodies using ELISA.

272 (+) T-cell cocultures were analyzed by using ELISA and flow cytometry.

273 Cytokine production was measured by using ELISA, and real-time quantitative PCR was performed to d

274 nd cellular analysis were performed by using ELISA, ELISpot, and flow cytometry.

275 ing flexiVent; inflammatory indices by using ELISA, histology, and real-time PCR; and type 2 innate l

276 By using ELISA, mean +/- SD levels of IgE-anti-IL-24 were 0.52 +/

277 and leukotriene E4 levels was done by using ELISA.

278 nd the level of PTX3 was determined by using ELISA.

279 D-specific IgE levels were analyzed by using ELISA.

280 by cultured B cells were quantified by using ELISA.

281 allergen specific IgE antibody levels using ELISA.

282 DKK-1 levels in plasma were measured using ELISA, and data analyzed with one-way ANOVA, logistic re

283 sera in patients with RA was measured using ELISA.

284 n levels of dust samples were measured using ELISA.

285 thylation level (%5-mC) was quantified using ELISA method.

286 by ELISA, insulin secretion quantified using ELISA or radioimmunoassay, and glucose uptake determined

287 Despite its utility, ELISA is time-consuming, resource-intensive, and infrast

288 by using quantitative PCR and apoptosis via ELISA.

289 ctivin A levels in the NAc were assessed via ELISA and immunohistochemistry (in neurons, astrocytes,

290 ubsequently verified their Ag reactivity via ELISA.

291 with low HGF levels in these tumors (ex vivo ELISA).

292 , validating to be an alternative to 96-well ELISA microplate for food safety monitoring.

293 This is in agreement with ELISA inhibition results showing that, although cross-re

294 analytical device (muPAD) was combined with ELISA and the intrinsic properties of paper allowed the

295 ere enriched in these areas, consistent with ELISA results.

296 e supernatants of activated macrophages with ELISA.

297 validated against the response measured with ELISA at a certified laboratory using serum from the sam

298 improved with respect to those obtained with ELISA kits.

299 nd EBOV, respectively, compared to that with ELISA.

300 n contrast, comparison of the Euroimmun ZIKV ELISA to either the CDC or InBios MAC-ELISAs resulted in