ライフサイエンスコーパス: enzyme-linked immunosorbent assay

1 relation to its antigenicity (determined by Enzyme-linked Immunosorbent Assay).

2 assay); 3) inflammatory cytokine synthesis (enzyme-linked immunosorbent assay).

3 y T cells were analyzed by flow cytometry or enzyme-linked immunosorbent assay.

4 ssed in saliva of healthy donors (n = 21) by enzyme-linked immunosorbent assay.

5 ow cytometry, cytokine multiplex assays, and enzyme-linked immunosorbent assay.

6 in the NETs, we established a CitH3 specific enzyme-linked immunosorbent assay.

7 by microcomputed tomography, histology, and enzyme-linked immunosorbent assay.

8 idated a subset of identified antigens using enzyme-linked immunosorbent assay.

9 ospinal fluid using a commercially available enzyme-linked immunosorbent assay.

10 ion molecules were evaluated by fluorometric enzyme-linked immunosorbent assay.

11 ucible protein 10 (IP-10) were quantified by enzyme-linked immunosorbent assay.

12 for production of inflammatory mediators by enzyme-linked immunosorbent assay.

13 nd chemokines using a 17-plex Luminex kit or enzyme-linked immunosorbent assay.

14 amily (IL1alpha, IL1beta, IL1ra, and IL6) by enzyme-linked immunosorbent assay.

15 s were assayed by a single antibody sandwich enzyme-linked immunosorbent assay.

16 -like particle-based immunoglobulin G direct enzyme-linked immunosorbent assay.

17 G) levels by an L1 virus-like particle-based enzyme-linked immunosorbent assay.

18 es of rat liver, kidney, and aorta, using an enzyme-linked immunosorbent assay.

19 unoglobulin A (IgA) level was measured by an enzyme-linked immunosorbent assay.

20 contents were determined by western blot and enzyme-linked immunosorbent assay.

21 interleukin 22 in serum from 28 patients by enzyme-linked immunosorbent assay.

22 MS mass spectrometry, 2D-gel analysis and by enzyme-linked immunosorbent assay.

23 MMP-8, and MMP-13 levels were measured using enzyme-linked immunosorbent assay.

24 immunocapture mass spectrometry and sandwich enzyme-linked immunosorbent assay.

25 and -BP-2b pilus proteins were determined by enzyme-linked immunosorbent assay.

26 mentous hemagglutinin (FHA) were assessed by enzyme-linked immunosorbent assay.

27 a antibody using whole-cell and glycoprotein enzyme-linked immunosorbent assay.

28 ies to all 3 MMR antigens were measured with enzyme-linked immunosorbent assay.

29 ase (GPX) levels in serum were measured with enzyme-linked immunosorbent assay.

30 using an anti-Psl monoclonal antibody (mAb) enzyme-linked immunosorbent assay.

31 and plasma levels of TGM-2 were analyzed by enzyme-linked immunosorbent assay.

32 verting enzyme and lysozyme were analyzed by enzyme-linked immunosorbent assay.

33 Levels of biomarkers were measured by enzyme-linked immunosorbent assay.

34 and PPP using a proteome profiler array and enzyme-linked immunosorbent assay.

35 )-alpha and interleukin (IL)-1beta levels by enzyme-linked immunosorbent assay.

36 -derived neurotrophic factor was assessed by enzyme-linked immunosorbent assay.

37 r retrospective testing for illicit drugs by enzyme-linked immunosorbent assay.

38 vels were assessed in peripheral blood by an enzyme-linked immunosorbent assay.

39 Inflammatory cytokines were measured by enzyme-linked immunosorbent assay.

40 Tear serotonin levels were measured using enzyme-linked immunosorbent assay.

41 e inhibitor of metalloproteinase (TIMP)-1 by enzyme-linked immunosorbent assay.

42 with immunoglobulin (Ig) G dye test and IgM enzyme-linked immunosorbent assay.

43 by a group A-specific immunoglobulin G (IgG) enzyme-linked immunosorbent assay.

44 F73 assay and VWF antigen (VWF:Ag) levels by enzyme-linked immunosorbent assay.

45 atients, NGF protein levels were measured by enzyme-linked immunosorbent assay.

46 n-inducing ligand (APRIL) were determined by enzyme-linked immunosorbent assay.

47 tin were evaluated at all time points, using enzyme-linked immunosorbent assay.

48 subclass response was characterized using an enzyme-linked immunosorbent assay.

49 mples) when combined with the IgG anti-BP180 enzyme-linked immunosorbent assay.

50 eafter, for up to 18 months, for analysis by enzyme-linked immunosorbent assay.

51 logically and TNF protein levels measured by enzyme-linked immunosorbent assay.

52 and MMP-2/TIMP-2 complex were assessed using enzyme-linked immunosorbent assay.

53 Serum Klotho level was measured by enzyme-linked immunosorbent assay.

54 atase (BALP) serum levels were determined by enzyme-linked immunosorbent assay.

55 Serum JCV antibody status was determined by enzyme-linked immunosorbent assay.

56 rrow, and lymph fluid were measured using an enzyme-linked immunosorbent assay.

57 with or without reactions were conducted via enzyme-linked immunosorbent assay.

58 VEGF-A protein expression was determined by enzyme-linked immunosorbent assay.

59 Sulfonylurea receptor- 1 was quantified by enzyme-linked immunosorbent assay.

60 were measured in patient synovial fluids by enzyme-linked immunosorbent assay.

61 and interleukin 6 (IL-6) were measured with enzyme-linked immunosorbent assay.

62 burgdorferi or autoantigens were measured by enzyme-linked immunosorbent assay.

63 rum was tested with the use of anti-ZIKV IgM enzyme-linked immunosorbent assay.

64 Salivary levels of analytes were analyzed by enzyme-linked immunosorbent assay.

65 antigen levels were measured with the Wantai enzyme-linked immunosorbent assay.

66 s were drawn to determine Abeta levels using enzyme-linked immunosorbent assay.

67 e chain reaction and an IgM antibody-capture enzyme-linked immunosorbent assay.

68 l disease, were not elevated by quantitative enzyme-linked immunosorbent assay.

69 ith acetaminophen-induced liver injury using enzyme-linked immunosorbent assays.

70 saliva, and serum by immunofluorometric and enzyme-linked immunosorbent assays.

71 F-1, MIF, MIG, and MMP-8 were measured using enzyme-linked immunosorbent assays.

72 employed for medical diagnostics, such as in enzyme-linked immunosorbent assays.

73 L)-1beta/IL-1 receptor antagonist (ra) using enzyme-linked immunosorbent assays.

74 gG) measured by qualitative and quantitative enzyme-linked immunosorbent assays.

75 genous antibody levels were assessed using 2 enzyme-linked immunosorbent assays.

76 nic cytokine level via proteome profiler and enzyme-linked immunosorbent assays.

77 following serum levels were determined using enzyme-linked immunosorbent assay: 1) IL-1beta; 2) IL-6;

78 s had positive antiplatelet factor 4/heparin enzyme-linked immunosorbent assay; 10 patients were iden

79 n (LOD) than observed with the gold standard enzyme-linked immunosorbent assay - a decrease from 23pg

80 Peptides were tested in enzyme-linked immunosorbent assays against celiac diseas

81 erase chain reaction [PCR]) and serological (enzyme-linked immunosorbent assay) analyses were perform

82 protein 1 (DKK-1), and beta-catenin; and by enzyme-linked immunosorbent assay analysis of myeloperox

83 ations in multiple tissues were estimated by enzyme-linked immunosorbent assay analysis.

84 n two markedly different platforms, being an enzyme-linked immunosorbent assay and a surface plasmon

85 r Borrelia burgdorferi (IgG as determined by enzyme-linked immunosorbent assay and confirmed by immun

86 opsies were assayed for urinary CXCL10 using enzyme-linked immunosorbent assay and corrected with uri

87 t of TF in tumor homogenates was measured by enzyme-linked immunosorbent assay and correlated with th

88 ne responses to immunization, as assessed by enzyme-linked immunosorbent assay and enzyme-linked immu

89 We now demonstrate by competitive enzyme-linked immunosorbent assay and hydrogen-deuterium

90 ession of signaling molecules was studied by enzyme-linked immunosorbent assay and immunoblotting.

91 By enzyme-linked immunosorbent assay and immunofluorescence

92 e compared findings of 2 orthogonal methods, enzyme-linked immunosorbent assay and mass spectrometry,

93 and underwent antiplatelet factor 4/heparin enzyme-linked immunosorbent assay and serotonin release

94 markers of oxidative stress were measured by enzyme-linked immunosorbent assay and spectrophotometric

95 Levels of MIC1 were measured by enzyme-linked immunosorbent assay and then were categori

96 Cortactin antibodies were measured by enzyme-linked immunosorbent assay and Western blot; AChR

97 led diagnostic testing for these diseases by enzyme-linked immunosorbent assays and dissection of var

98 KV, dengue virus, and chikungunya virus; IgM enzyme-linked immunosorbent assays and plaque-reduction

99 were measured at baseline using quantitative enzyme-linked immunosorbent assays and used to stratify

100 Anti-CMV IgG was measured by enzyme-linked immunosorbent assay, and CMV DNA by polyme

101 suPAR was measured by enzyme-linked immunosorbent assay, and events of comorbi

102 -specific antibody levels were analyzed with enzyme-linked immunosorbent assay, and frequency of memo

103 mRNA extraction, real-time quantitative PCR, enzyme-linked immunosorbent assay, and immunohistochemic

104 Gene expression analysis, enzyme-linked immunosorbent assay, and immunohistochemis

105 raphy tandem mass spectrometry, confirmed by enzyme-linked immunosorbent assay, and localized by conf

106 phritic urine by dipstick and albuminuria by enzyme-linked immunosorbent assay, and monocyte depletio

107 histology, immunohistochemical, immunoblot, enzyme-linked immunosorbent assay, and quantitative poly

108 ients had 4Ts, antiplatelet factor 4/heparin enzyme-linked immunosorbent assay, and serotonin release

109 Visfatin levels were analyzed by enzyme-linked immunosorbent assay, and the bacterial num

110 llagen III N-terminal propeptide (PIIINP) by enzyme-linked immunosorbent assay, and urinary lipoarabi

111 reaction, immunoblot, immunohistochemistry, enzyme-linked immunosorbent assays, and metabolite assay

112 ion were assessed for Ab responses to AM via enzyme-linked immunosorbent assays, and to AM OS epitope

113 amyloid-beta42 using a Meso Scale Discovery enzyme linked immunosorbent assay; and (iii) cerebrospin

114 eagents with good results in the competitive enzyme-linked immunosorbent assay are often unable to pr

115 larization with a glass chip-based multiplex enzyme-linked immunosorbent assay array and in vitro imm

116 kin-17A, and interleukin-10 were measured by enzyme-linked immunosorbent assay at each time point and

117 and interleukin (IL)-1beta were evaluated by enzyme-linked immunosorbent assay at week 17.

118 molecule 1 [VCAM-1]) were measured by using enzyme-linked immunosorbent assays at 1 day, 2 weeks, an

119 asis of involvement in relevant pathways and enzyme-linked immunosorbent assay availability.

120 ) antibody, glycoprotein B-, C-, and D-based enzyme-linked immunosorbent assays (B-, C-, and D-ELISAs

121 The hybrid library was screened by enzyme-linked immunosorbent assay-based kinase inhibitio

122 Measles antibody titers were measured by enzyme-linked immunosorbent assay before and after each

123 ndirect immunofluorescent assays [IFA] and 2 enzyme-linked immunosorbent assays-both HHV8 lytic and l

124 t detectable anti-GM1 IgM antibody titers in enzyme-linked immunosorbent assay, but not with sera fro

125 Low-detergent extracts tested by 82E1 enzyme-linked immunosorbent assay confirmed the presence

126 tomography and (i) multi-laboratory INNOTEST enzyme linked immunosorbent assay derived cerebrospinal

127 entified 34 PCV3-positive cases (12.5%), and enzyme-linked immunosorbent assay detection of anti-PCV3

128 to derive polyclonal antibodies for RDT and enzyme-linked immunosorbent assay development.

129 this work, we describe an electronics-based Enzyme-Linked ImmunoSorbent Assay (eELISA), using a Lab-

130 A novel immunoassay based on specific enzyme linked immunosorbent assay (ELISA) combined with

131 concentration of CYFRA-21-1 obtained through enzyme linked immunosorbent assay (ELISA) in saliva samp

132 Enzyme linked immunosorbent assay (ELISA) is one of the

133 athogen detection methods such as culturing, enzyme linked immunosorbent assay (ELISA) or polymerase

134 x of the protein fractions using competitive enzyme linked immunosorbent assay (ELISA) technique and

135 also confirmed by other spectral methods and enzyme linked immunosorbent assay (ELISA).

136 The observed results have been validated via enzyme linked immunosorbent assay (ELISA).

137 on systems, including gelatin zymography and enzyme linked immunosorbent assay (ELISA).

138 ipients had seroconversion as assessed by an enzyme-linked immunosorbent assay (ELISA) against the gl

139 (i) cellulose-coated microarray assay, (ii) enzyme-linked immunosorbent assay (ELISA) and (iii) in-v

140 Through an enzyme-linked immunosorbent assay (ELISA) and a histo-bl

141 ation twice weekly by use of a commercial GM enzyme-linked immunosorbent assay (ELISA) and a PCR assa

142 ity in rabbits and assessed the responses by enzyme-linked immunosorbent assay (ELISA) and competitio

143 rough an F. hepatica-specific serum antibody enzyme-linked immunosorbent assay (ELISA) and fluke egg

144 ranges are considerably wider than those of enzyme-linked immunosorbent assay (ELISA) and other immu

145 using alga-produced recombinant Pfs25 as the enzyme-linked immunosorbent assay (ELISA) antigen.

146 Immunoassays such as the enzyme-linked immunosorbent assay (ELISA) are commonly u

147 onal competitive immunoassay formats such as enzyme-linked immunosorbent assay (ELISA) are the specif

148 ested for antibodies to AT1R and ETAR by the enzyme-linked immunosorbent assay (ELISA) assay.

149 cy of the results with those obtained by the enzyme-linked immunosorbent assay (ELISA) conventional m

150 Enzyme-linked immunosorbent assay (ELISA) demonstrates m

151 Recently, an anti-HEV antigen (Ag)-specific enzyme-linked immunosorbent assay (ELISA) directed again

152 IFN-gamma release was measured by enzyme-linked immunosorbent assay (ELISA) following over

153 We used Fab/scFv in the context of an enzyme-linked immunosorbent assay (ELISA) for HBeAg quan

154 Here, we developed a sensitive sandwich enzyme-linked immunosorbent assay (ELISA) for PEG by tet

155 ns were analyzed via histologic analysis and enzyme-linked immunosorbent assay (ELISA) for quantifica

156 A sensitive, competitive enzyme-linked immunosorbent assay (ELISA) for the detect

157 lop a highly specific and sensitive sandwich enzyme-linked immunosorbent assay (ELISA) for the detect

158 d a high-throughput, objective peptide-based enzyme-linked immunosorbent assay (ELISA) for use alone

159 Using a novel enzyme-linked immunosorbent assay (ELISA) format as a sc

160 quality, whereas those for the Ortho HCV Ag enzyme-linked immunosorbent assay (ELISA) had the lowest

161 The enzyme-linked immunosorbent assay (ELISA) has been propo

162 ce VTPNDDTFDPFR, showed the best response in enzyme-linked immunosorbent assay (ELISA) in terms of se

163 Enzyme-linked immunosorbent assay (ELISA) is a valuable

164 Enzyme-linked immunosorbent assay (ELISA) is one of the

165 The application of antibodies in enzyme-linked immunosorbent assay (ELISA) is the basis o

166 Enzyme-linked immunosorbent assay (ELISA) measurements o

167 The enzyme-linked immunosorbent assay (ELISA) method consist

168 the developed OWLS immunosenor with HPLC and enzyme-linked immunosorbent assay (ELISA) methods for th

169 Enzyme-linked immunosorbent assay (ELISA) performed on s

170 An enzyme-linked immunosorbent assay (ELISA) quantified clo

171 hSBA, rSBA, and immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) results were c

172 cortisol sensor chip was validated using an enzyme-linked immunosorbent assay (ELISA) technique with

173 This study developed an enzyme-linked immunosorbent assay (ELISA) to detect anti

174 We developed an enzyme-linked immunosorbent assay (ELISA) to measure the

175 ents using a proteomics approach followed by enzyme-linked immunosorbent assay (ELISA) validation.

176 in conventional dengue NS1 capture using an enzyme-linked immunosorbent assay (ELISA) was applied to

177 In this study, a paper-based microfluidic enzyme-linked immunosorbent assay (ELISA) was developed

178 A quantitative Enzyme-Linked ImmunoSorbent Assay (ELISA) was formatted

179 although successful detection with the rapid enzyme-linked immunosorbent assay (ELISA) was more varia

180 Chlamydia trachomatis elementary body enzyme-linked immunosorbent assay (ELISA) was used to in

181 The computationally designed enzyme-linked immunosorbent assay (ELISA) was validated

182 90%) was found in 5 tests only: polyspecific enzyme-linked immunosorbent assay (ELISA) with intermedi

183 his performance came close to a conventional enzyme-linked immunosorbent assay (ELISA) without the ne

184 , osmotic shock increased cBIN1 detection by enzyme-linked immunosorbent assay (ELISA), and cBIN1 lev

185 valuated for reactivity to E-pore peptide by enzyme-linked immunosorbent assay (ELISA), and histology

186 ugh, available methods such as neuroimaging, enzyme-linked immunosorbent assay (ELISA), and polymeras

187 ed by flow cytometry, cytokines by multiplex enzyme-linked immunosorbent assay (ELISA), and the micro

188 The first-tier test is a low-specificity enzyme-linked immunosorbent assay (ELISA), and the secon

189 icroarray analysis, quantitative PCR (qPCR), enzyme-linked immunosorbent assay (ELISA), and Western b

190 performed by centralized laboratories using Enzyme-Linked ImmunoSorbent Assay (ELISA), faster on-sit

191 Enzyme-linked immunosorbent assay (ELISA), flow cytometr

192 developed human C-reactive protein sandwich enzyme-linked immunosorbent assay (ELISA), horseradish p

193 all-in-one dual-aptasensor and conventional enzyme-linked immunosorbent assay (ELISA), operated with

194 -SPR were compared to a clinically validated enzyme-linked immunosorbent assay (ELISA), resulting in

195 Using enzyme-linked immunosorbent assay (ELISA), we obtain ser

196 An enzyme-linked immunosorbent assay (ELISA)-like method ba

197 the modified antibody was confirmed using an enzyme-linked immunosorbent assay (ELISA)-type binding a

198 d and analyzed for NE using a single-analyte enzyme-linked immunosorbent assay (ELISA).

199 y neutralization assay (CCNA) and tgcBIOMICS enzyme-linked immunosorbent assay (ELISA).

200 shorter turnaround time compared to standard enzyme-linked immunosorbent assay (ELISA).

201 SVA VP1 recombinant protein (rVP1) indirect enzyme-linked immunosorbent assay (ELISA).

202 P) in human serum via a miniature bead-based enzyme-linked immunosorbent assay (ELISA).

203 anti-PrP(Sc) specific antibodies by indirect enzyme-linked immunosorbent assay (ELISA).

204 ytical device that can be used to conduct an enzyme-linked immunosorbent assay (ELISA).

205 quent detection of dengue enveloped virus in enzyme-linked immunosorbent assay (ELISA).

206 analyzed by flow cytometry, and cytokines by enzyme-linked immunosorbent assay (ELISA).

207 ative approach for an automated and one-step enzyme-linked immunosorbent assay (ELISA).

208 of antibodies to all viruses as measured by enzyme-linked immunosorbent assay (ELISA).

209 using quantitative PCR, immunoblotting, and enzyme-linked immunosorbent assay (ELISA).

210 ion sensitivity is as good as or better than enzyme-linked immunosorbent assay (ELISA).

211 for hemorrhagic fever detection has been the enzyme-linked immunosorbent assay (ELISA); however, newe

212 es used to detect pathogens in plant include enzyme-linked immunosorbent assays (ELISA) and direct ti

213 ever, a major weakness inherent to multiplex enzyme-linked immunosorbent assays (ELISA) is generation

214 sm or Alzheimer's disease were quantified by enzyme-linked immunosorbent assays (ELISA) or theoretica

215 which collected demographic information and enzyme-linked immunosorbent assays (ELISA) which tested

216 t anti-FLAG IgG antibodies in the subsequent enzyme-linked immunosorbent assays (ELISA), and yielded

217 Various existing techniques such as enzyme-linked immunosorbent assays (ELISA), Western blot

218 derived Lb8E and Lb6H, and evaluated both in enzyme-linked immunosorbent assays (ELISA).

219 ) were measured using commercially available enzyme-linked immunosorbent assays (ELISA).

220 ding mass spectrometry (LB-MS) in support of enzyme-linked immunosorbent assays (ELISA).

221 We monitored the cytokine profile (using enzyme-linked immunosorbent assay [ELISA]), reactive oxy

222 common allergen detection methods, including enzyme-linked immunosorbent assays (ELISAs) and dip-stic

223 Combined with enzyme-linked immunosorbent assays (ELISAs) and fluoresc

224 Enzyme-linked immunosorbent assays (ELISAs) based on ZIK

225 The different enzyme-linked immunosorbent assays (ELISAs) for gluten d

226 be 1,000-fold more sensitive than classical enzyme-linked immunosorbent assays (ELISAs) in the quant

227 Competition enzyme-linked immunosorbent assays (ELISAs) showed that

228 nd reduce the time for diagnosis, four rapid enzyme-linked immunosorbent assays (ELISAs) were develop

229 R), for detection of DENV serotypes 1-4, and enzyme-linked immunosorbent assays (ELISAs), for detecti

230 erkinElmer Optiplate96 well plate for use in enzyme-linked immunosorbent assays (ELISAs).

231 iological activity and detection in standard enzyme-linked immunosorbent assays (ELISAs).

232 ltigravid women and then characterized using enzyme-linked immunosorbent assay, flow cytometry, and a

233 chemokines, and antibodies were measured by enzyme-linked immunosorbent assay, flow cytometry, or mu

234 ed noninferiority of HPV-16/18 antibodies by enzyme-linked immunosorbent assay for 2D (M0,6) versus 3

235 asma from healthy blood donors was tested by enzyme-linked immunosorbent assay for anti-HCMV immunogl

236 Sixty-five patients with BP underwent an enzyme-linked immunosorbent assay for IgE antibodies aga

237 and demonstrated a high correlation with an enzyme-linked immunosorbent assay for sample detection i

238 An IgM antibody-capture enzyme-linked immunosorbent assay for ZIKV was performed

239 GCF was analyzed via enzyme-linked immunosorbent assay for: 1) receptor activ

240 specific immune responses using glycoprotein enzyme-linked immunosorbent assay (gpELISA) and interfer

241 titers (measured by a VZV glycoprotein-based enzyme-linked immunosorbent assay [gpELISA]) and levels

242 Urinary calprotectin was assessed by enzyme-linked immunosorbent assay in 328 subjects includ

243 Concentration of CXCL13 was determined with enzyme-linked immunosorbent assay in all available patie

244 pithelial cells were investigated by PCR and enzyme-linked immunosorbent assay in an in vitro diabete

245 expression was analyzed using RT-qPCR and/or enzyme-linked immunosorbent assay in T-cell subsets and

246 6, and TNF-alpha levels were estimated using enzyme-linked immunosorbent assays in GCF and serum samp

247 cted to validate in 489 coke-oven workers by enzyme-linked immunosorbent assays in validation stage.

248 If antiplatelet factor 4/heparin enzyme-linked immunosorbent assay is used to consider im

249 faster IA, compared to a commercial sandwich enzyme-linked immunosorbent assay kit.

250 faster IA, compared to a commercial sandwich enzyme-linked immunosorbent assay kit.

251 Samples were tested by commercial enzyme-linked immunosorbent assay kits for immunoglobuli

252 reen using an anti-ZIKV IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) followed b

253 serologically, using an IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) for screen

254 velope (prM/E)-specific IgM antibody-capture enzyme-linked immunosorbent assay (MAC-ELISA).

255 teral flow rapid tests, IgM antibody capture enzyme-linked immunosorbent assays (MAC-ELISAs), and ind

256 the precise mass spectrometry method than by enzyme-linked immunosorbent assay (mean difference of SD

257 and TNF-alpha levels were analyzed using an enzyme-linked immunosorbent assay method.

258 ield validation in Panama and compared to an enzyme-linked immunosorbent assay/Multispot-based testin

259 We performed a cytokine enzyme-linked immunosorbent assay of serum samples from

260 s (81.8%) with antiplatelet factor 4/heparin enzyme-linked immunosorbent assay optical density greate

261 aging a higher antiplatelet factor 4/heparin enzyme-linked immunosorbent assay optical density thresh

262 ntly higher heparin-induced thrombocytopenia enzyme-linked immunosorbent assays optical density; had

263 both positive antiplatelet factor 4/heparin enzyme-linked immunosorbent assay (optical density, >/=

264 ches with various detection techniques (e.g. enzyme-linked immunosorbent assay or ELISA) on solid sta

265 milk samples of mothers were measured using enzyme-linked immunosorbent assays or a microneutralizat

266 his device shows great promise toward use in enzyme-linked immunosorbent assays or other analytical t

267 e no discernible inhibitory effects in model enzyme-linked immunosorbent assays or polymerase chain r

268 Compared to the enzyme-linked immunosorbent assay, our method is label-f

269 IL-6 levels were assayed using an enzyme linked immunosorbent assay preoperatively, and at

270 Enzyme immunoassay determined LTB4, and enzyme-linked immunosorbent assays quantified tumor necr

271 DMCL efficacy positively correlated with the enzyme-linked immunosorbent assay-reactive intensity of

272 vely coupled plasma mass spectrometry and an enzyme-linked immunosorbent assay, respectively.

273 and for serum protein levels by Luminex and enzyme-linked immunosorbent assays, respectively.

274 ding age, sex, antiplatelet factor 4/heparin enzyme-linked immunosorbent assay, serotonin release ass

275 ed herein based on biosensor experiments and enzyme-linked immunosorbent assays shows that the DnaB-D

276 Immunoblotting and enzyme-linked immunosorbent assay studies of the patient

277 asma samples collected in 211 patients using enzyme-linked immunosorbent assay (Tac/Sir = 104, Tac/Mt

278 eso Scale Discovery electrochemiluminescence enzyme linked immunosorbent assay technology, and a nove

279 Because ALP is widely used in enzyme-linked immunosorbent assays, the probe was couple

280 iters (approximately 20-fold from the median enzyme-linked immunosorbent assay titers of 30-300 to 30

281 We utilized fluorescence microscopy and enzyme-linked immunosorbent assay to analyze the distrib

282 We used microchannel enzyme-linked immunosorbent assay to evaluate the functi

283 We used enzyme-linked immunosorbent assay to measure endogenous

284 collected and analyzed histologically or by enzyme-linked immunosorbent assays to measure cytokine l

285 sitivity rates, defined by birth anti-PT >30 enzyme-linked immunosorbent assay units (EU)/mL to confe

286 LNA/DNA sequences showed improved binding in enzyme-linked immunosorbent assay using human samples of

287 al fluid for ZIKV using IgM antibody-capture enzyme-linked immunosorbent assay was performed in 24 of

288 Enzyme-linked immunosorbent assay was used to determine

289 Enzyme-linked immunosorbent assay was used to measure ch

290 A JCPyV VP1 enzyme-linked immunosorbent assay was used to measure pa

291 Using enzyme-linked immunosorbent assay, we analyzed serial se

292 Using a newly developed enzyme-linked immunosorbent assay, we evaluated circulat

293 Using enzyme-linked immunosorbent assay, we tested M65 and M30

294 , immunosuppression, and IgG aCL assessed by enzyme-linked immunosorbent assay were tested as potenti

295 reverse transcription-PCR and anti-DENV IgM enzyme-linked immunosorbent assay were used to verify RD

296 Plasma peptide YY and ghrelin (enzyme-linked immunosorbent assay) were measured once in

297 Serum VEGF protein levels were analyzed by enzyme-linked immunosorbent assay, whereas quantitative

298 survivors, 99 nonsurvivors) were analyzed by enzyme-linked immunosorbent assay with clinical data fro

299 Pre- and postinfection sera were assayed by enzyme-linked immunosorbent assay with N-terminal M pept

300 Comparative enzyme-linked immunosorbent assays with monoclonal antib