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

1 ry, real-time polymerase chain reaction, and enzyme-linked immunosorbent assay.

2 and 180 were assessed via flow cytometry and enzyme-linked immunosorbent assay.

3 sed by hemagglutination inhibition assay and enzyme-linked immunosorbent assay.

4 i-vaccine antibody titers were quantified by enzyme-linked immunosorbent assay.

5 glutination assay and a Competitive Indirect Enzyme-linked immunosorbent assay.

6 ns of PvMSP3alpha, were measured by means of enzyme-linked immunosorbent assay.

7 parum circumsporozoite protein (PfCSP) using enzyme-linked immunosorbent assay.

8 ts hospitalized with CAP were measured using enzyme-linked immunosorbent assay.

9 arvested to evaluate cytokine profiles using Enzyme-Linked Immunosorbent Assay.

10 oglobulin M (IgM) and immunoglobulin G (IgG) enzyme-linked immunosorbent assay.

11 s measured using a virus-like particle-based enzyme-linked immunosorbent assay.

12 ogens was determined in an in vitro model by enzyme-linked immunosorbent assay.

13 ated dUTP nick-end labeling and DNA fragment enzyme-linked immunosorbent assay.

14 PS-specific antibodies were determined using enzyme-linked immunosorbent assay.

15 D, PAD2, and MMP-8 levels were determined by enzyme-linked immunosorbent assay.

16 nd the HRP2 concentration was measured by an enzyme-linked immunosorbent assay.

17 nalyzed for anti-PEG-ASP immunoglobulin G by enzyme-linked immunosorbent assay.

18 ere analyzed using multiplex immunoassay and enzyme-linked immunosorbent assay.

19 oproteinase-2 (MMP-2) were measured using an enzyme-linked immunosorbent assay.

20 VEGF, and TNF-alpha levels were measured by enzyme-linked immunosorbent assay.

21 ntibodies by Crithidia luciliae staining and enzyme-linked immunosorbent assay.

22 Melatonin levels were determined by enzyme-linked immunosorbent assay.

23 Serum PRO-C3 was assessed by competitive, enzyme-linked immunosorbent assay.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 IL-1beta, and calprotectin were analyzed by enzyme-linked immunosorbent assay.

40 mens with a 62-cytokine multiplex bead-based enzyme-linked immunosorbent assay.

41 ied using a broadly reactive, genus-specific enzyme-linked immunosorbent assay.

42 ibody titer >=10 AU/mL using a drug-tolerant enzyme-linked immunosorbent assay.

43 istochemistry, western-blotting, and also by enzyme-linked immunosorbent assay.

44 The PC- and gB-specific ABs were assessed by enzyme-linked immunosorbent assay.

45 S-CoV-2 spike protein were detected by using enzyme-linked immunosorbent assay.

46 soluble FAS ligand (sFASL) were measured by enzyme-linked immunosorbent assay.

47 asured in cell culture supernatants using an enzyme-linked immunosorbent assay.

48 IgG antibodies and PGI and PGII levels using enzyme linked immunosorbent assays.

49 response to rATG was analyzed via multiplex enzyme-linked immunosorbent assays.

50 popolysaccharide (Pg-LPS) stimulation, using enzyme-linked immunosorbent assays.

51 1) were serially measured using quantitative enzyme-linked immunosorbent assays.

52 evicular fluid (GCF) of all participants via enzyme-linked immunosorbent assays.

53 aging, immunoblot, and functional assays and enzyme-linked immunosorbent assays.

54 tactin (PRN) were evaluated using commercial enzyme-linked immunosorbent assays.

55 ed by techniques based on flow cytometry and enzyme-linked immunosorbent assays.

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

57 Enzyme-linked immunosorbent assays against whole bacteri

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

59 IKV antibodies using a ZIKV immunoglobulin G enzyme-linked immunosorbent assay and a virus neutraliza

60 Several methods like enzyme-linked immunosorbent assay and affinity chromatog

61 l outgrowth was measured by the standard p24 enzyme-linked immunosorbent assay and an ultrasensitive

62 We measured levels of S100A8-A9 by enzyme-linked immunosorbent assay and analyzed fecal mic

63 and 7 were assayed for IL-1beta and IL-10 by enzyme-linked immunosorbent assay and compared using the

64 urnetii immunoreactive proteins validated by enzyme-linked immunosorbent assay and demonstrate the ef

65 mage, neurofilament light chain (NfL), using enzyme-linked immunosorbent assay and electrochemilumine

66 yze a semi-homogeneous bead-based electronic enzyme-linked immunosorbent assay and find that experime

67 mouse serum, we developed a highly sensitive enzyme-linked immunosorbent assay and found that HN3-ABD

68 We measured levels of IFNL by enzyme-linked immunosorbent assay and immunohistochemist

69 vels were further confirmed by Western blot, enzyme-linked immunosorbent assay and immunohistochemist

70 re screened by MERS-CoV nucleocapsid protein enzyme-linked immunosorbent assay and indirect immunoflu

71 repair, and growth factors with immunoassay (enzyme-linked immunosorbent assay and Luminex).

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

73 Enzyme-linked immunosorbent assay and microsphere-based

74 e also measured fecal pancreatic elastase by enzyme-linked immunosorbent assay and performed quantita

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

76 ction antibody titer (measured by inhibition enzyme-linked immunosorbent assay) and dengue severity,

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

78 10 was measured in serum samples by means of enzyme-linked immunosorbent assay, and coronary atherosc

79 IBS-D had increased levels of PGE2, based on enzyme-linked immunosorbent assay, and COX2 messenger RN

80 mmaRI binding via surface plasmon resonance, enzyme-linked immunosorbent assay, and flow cytometry.

81 factors were analyzed using immunostaining, enzyme-linked immunosorbent assay, and heparanase procoa

82 on factors were analyzed via immunostaining, enzyme-linked immunosorbent assay, and heparanase procoa

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

84 um samples were analyzed by gliadin antibody enzyme-linked immunosorbent assay, and intestinal tissue

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

86 DBS sample CRP measurements were made by enzyme-linked immunosorbent assay, and venepuncture samp

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

88 as performed with the use of protein arrays, enzyme-linked immunosorbent assays, and Western blot ana

89 Prospective determination of enzyme-linked immunosorbent assay anti-RBD IgG titer fac

90 sponses were higher with higher dose (day 29 enzyme-linked immunosorbent assay anti-S-2P antibody geo

91 Enzyme-linked immunosorbent assays are currently the mos

92 PE-PilA was found to bind vitronectin by enzyme-linked immunosorbent assay, as isolated PE does.

93 mmunoglobulin G titers were quantified using enzyme-linked immunosorbent assay at 4.5 years.

94 ng highly sensitive double antibody sandwich enzyme-linked immunosorbent assay at baseline and 2 week

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

96 NiV antibodies using a comparative indirect enzyme-linked immunosorbent assay based on the recombina

97 itory capacity were also explored through an enzyme-linked immunosorbent assay-based measurement of n

98 oglobulin G titers were measured by means of enzyme-linked immunosorbent assay before and 1 month aft

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

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

101 raphy, gas chromatography-mass spectrometry, enzyme-linked immunosorbent assay, capillary electrophor

102 T cell effector functions were determined by enzyme-linked immunosorbent assay, carboxyfluorescein su

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

104 Enzyme-linked immunosorbent assays determined highly sig

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

106 ercial COVID-19 antibody tests, including an enzyme linked immunosorbent assay (ELISA) and a Luminex-

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

108 dvance over the state of the art method, the enzyme linked immunosorbent assay (ELISA) used in clinic

109 fection stage rely on Gram stains, cultures, Enzyme linked immunosorbent assay (ELISA), polymerase ch

110 y, we established and used multiple indirect Enzyme Linked Immunosorbent Assay (ELISA)-based serologi

111 tions (PCR), lateral flow devices (LFID) and enzyme linked immunosorbent assays (ELISA) are being ada

112 etermine the diagnostic performance of a CRP enzyme-linked immunosorbent assay (ELISA) (Eurolyser) in

113 uantified the levels of tropomyosin by using enzyme-linked immunosorbent assay (ELISA) among raw and

114 In immunohistochemical and enzyme-linked immunosorbent assay (ELISA) analyses of ti

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

116 rformance of high complexity methods such as Enzyme-Linked Immunosorbent Assay (ELISA) and Chemilumin

117 Results of whole-bacterial-cell enzyme-linked immunosorbent assay (ELISA) and flow cytom

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

119 F-1alpha in GCF and serum were quantified by enzyme-linked immunosorbent assay (ELISA) and reported a

120 The second assay is enzyme-linked immunosorbent assay (ELISA) based and can

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

122 ecificity comparable or better than standard enzyme-linked immunosorbent assay (ELISA) directly from

123 anti-EBOV-specific IgM and IgG antibodies by enzyme-linked immunosorbent assay (ELISA) for 126 study

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

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

126 near million-fold improvement over standard enzyme-linked immunosorbent assay (ELISA) for protein de

127 ffusion (SRID), we report a new quantitative enzyme-linked immunosorbent assay (ELISA) for seasonal t

128 Then, we applied it in an ultrasensitive enzyme-linked immunosorbent assay (ELISA) for the detect

129 dapted a commercially available, serum-based enzyme-linked immunosorbent assay (ELISA) for use with s

130 ZEBOV-GP enzyme-linked immunosorbent assay (ELISA) geometric mean

131 Enzyme-linked immunosorbent assay (ELISA) is a widely us

132 Enzyme-linked immunosorbent assay (ELISA) is a widely us

133 The enzyme-linked immunosorbent assay (ELISA) is commonly us

134 Enzyme-linked immunosorbent assay (ELISA) is the gold st

135 ficult to quantify using currently available enzyme-linked immunosorbent assay (ELISA) kits and, ther

136 lower than those obtained with conventional enzyme-linked immunosorbent assay (ELISA) methodologies

137 osen for validation through a CXCL12 protein enzyme-linked immunosorbent assay (ELISA) on patient ser

138 We assessed cytokine production via enzyme-linked immunosorbent assay (ELISA) or V-Plex, and

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

140 Competitive enzyme-linked immunosorbent assay (ELISA) studies showed

141 Moreover, enzyme-linked immunosorbent assay (ELISA) tests were neg

142 formed using serological techniques like the enzyme-linked immunosorbent assay (ELISA) to detect anti

143 h focused on the pathway toward a recognized enzyme-linked immunosorbent assay (ELISA) to determine s

144 ative to the natural enzyme in a traditional enzyme-linked immunosorbent assay (ELISA) to establish a

145 of adding the Toxoplasma gondii IgA antibody enzyme-linked immunosorbent assay (ELISA) to the serolog

146 ses with IgG titers reaching several million enzyme-linked immunosorbent assay (ELISA) units.

147 etecting Plasmodium antigen in a fluorescent enzyme-linked immunosorbent assay (ELISA) using a fluore

148 We evaluated these antigens by enzyme-linked immunosorbent assay (ELISA) using sera fro

149 prototype biosensor was compared to standard enzyme-linked immunosorbent assay (ELISA) using unstimul

150 has sensitivity superior to that of the Zeus enzyme-linked immunosorbent assay (ELISA) VZV IgG assay

151 This enzyme-linked immunosorbent assay (ELISA) was based on s

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

153 A novel enzyme-linked immunosorbent assay (ELISA) was developed

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

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

156 umps, measles, and rubella determined by IgG enzyme-linked immunosorbent assay (ELISA) were 93, 93, a

157 um samples, as well as 44 serum samples from enzyme-linked immunosorbent assay (ELISA) West Nile- and

158 va of OSCC patients from healthy subjects by enzyme-linked immunosorbent assay (ELISA) with sensitivi

159 sively among the following 4 patient groups: enzyme-linked immunosorbent assay (ELISA)+/serotonin-rel

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

161 identified IBV-M41 receptor was confirmed by enzyme-linked immunosorbent assay (ELISA), demonstrating

162 APP metabolite levels were determined by enzyme-linked immunosorbent assay (ELISA), for Human Abe

163 age matrix-related proteins were assessed by enzyme-linked immunosorbent assay (ELISA), histology, an

164 romatography-Mass Spectrometry (UPLC-MS) and Enzyme-Linked Immunosorbent Assay (ELISA), including hig

165 overall HCP levels are usually monitored by enzyme-linked immunosorbent assay (ELISA), liquid chroma

166 mania research diagnostics utilized included enzyme-linked immunosorbent assay (ELISA), rk39 test str

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

168 functional neutralizing antibodies), and the enzyme-linked immunosorbent assay (ELISA), which measure

169 Here, we developed a simple enzyme-linked immunosorbent assay (ELISA)-based assay th

170 inst serum samples, compared to conventional enzyme-linked immunosorbent assay (ELISA).

171 nd sera for SARS-CoV-2 antibodies testing by enzyme-linked immunosorbent assay (ELISA).

172 HBGA phenotype was determined by salivary enzyme-linked immunosorbent assay (ELISA).

173 to Pf circumsporozoite protein (PfCSP) using enzyme-linked immunosorbent assay (ELISA).

174 PCLS function was quantified by albumin enzyme-linked immunosorbent assay (ELISA).

175 d in NOD/ShiLtJ using metabololipidomics and enzyme-linked immunosorbent assay (ELISA).

176 use as serodiagnostic antigen in an indirect enzyme-linked immunosorbent assay (ELISA).

177 (42)) of P. vivax and P. falciparum using an enzyme-linked immunosorbent assay (ELISA).

178 Cytokine levels were assayed via multiplex enzyme-linked immunosorbent assay (ELISA).

179 imab-TNF complexes and ADAs were measured by enzyme-linked immunosorbent assay (ELISA).

180 cloprid concentrations were determined by an enzyme-linked immunosorbent assay (ELISA).

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

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

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

184 mAb-EspB-B7 and validated it by competitive enzyme-linked immunosorbent assay (ELISA).

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

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

187 ) participants (n=297), we measured apo M by Enzyme-Linked ImmunoSorbent Assay (ELISA).

188 tensin II) in the plasma were measured by an enzyme-linked immunosorbent assay (ELISA).

189 pecific antibodies were measured by means of enzyme-linked immunosorbent assay (ELISA).

190 covery method, which was further compared to enzyme-linked immunosorbent assay (ELISA).

191 a conventional detection method, such as an enzyme-linked immunosorbent assay (ELISA).

192 a3 (C6Malpha3) and employed in a competitive enzyme-linked immunosorbent assay (ELISA).

193 ed by a commercial SARS-CoV-2 total antibody enzyme-linked immunosorbent assay (ELISA, Wantai Biologi

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

195 Plasmonic enzyme-linked immunosorbent assays (ELISA) using the loc

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

197 ed Enpp1 and Impdh2, which were validated by enzyme-linked immunosorbent assays (ELISA).

198 tactin (PRN) were evaluated using commercial enzyme-linked immunosorbent assays (ELISA).

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

200 means of lateral-flow rapid test as well as enzyme-linked-immunosorbent-assay (ELISA).

201 ety; and IgG anti-spike protein response (in enzyme-linked immunosorbent assay [ELISA] units).

202 Three enzyme-linked immunosorbent assays (ELISAs) (Hemagen, Or

203 sitivities and specificities of 4 commercial enzyme-linked immunosorbent assays (ELISAs) and 2 rapid

204 able SARS-CoV-2 detection tests and in-house enzyme-linked immunosorbent assays (ELISAs) and correlat

205 bound to heparin and chondroitin sulfate in enzyme-linked immunosorbent assays (ELISAs) and depended

206 We reported previously that enzyme-linked immunosorbent assays (ELISAs) based on the

207 Enzyme-linked immunosorbent assays (ELISAs) for BP180 an

208 GST pulldown and indirect enzyme-linked immunosorbent assays (ELISAs) further conf

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

210 niae serum antibody detection via commercial enzyme-linked immunosorbent assays (ELISAs) is widely us

211 activities to a panel of class 5 adhesins in enzyme-linked immunosorbent assays (ELISAs) revealed sev

212 and compared to three commercially available enzyme-linked immunosorbent assays (ELISAs) targeting th

213 IgG1 or IgG enzyme-linked immunosorbent assays (ELISAs) with rK39 or

214 Instead, using immunoblotting and enzyme-linked immunosorbent assays (ELISAs), we found th

215 raction with soluble dimeric FcgammaRIIIa in enzyme-linked immunosorbent assays (ELISAs).

216 obtained using quantitative, single-plexed, enzyme-linked immunosorbent assays (ELISAs).

217 of autoimmune diseases routinely detected by enzyme-linked immunosorbent assays (ELISAs).

218 phic factor (GDNF) were analysed by specific enzyme-linked immunosorbent assays (ELISAs).

219 he full use of double nanobodies in sandwich enzyme-linked immunosorbent assays (ELISAs).

220 lis somatic antigens ("crude antigen") using enzyme-linked immunosorbent assays (ELISAs).

221 ralization, and immunoglobulin A (IgA) and G enzyme-linked immunosorbent assays (ELISAs); NPW specime

222 Using an indirect enzyme-linked immunosorbent assay for all 5 muscarinic r

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

224 Serum samples were also screened by means of enzyme-linked immunosorbent assay for antibodies reactiv

225 nase assay performed for cell damage, and an enzyme-linked immunosorbent assay for cytokine expressio

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

227 ents with a total of 197 specimens tested by enzyme-linked immunosorbent assay for IgM, IgG, and IgA

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

229 Here, we describe a serological enzyme-linked immunosorbent assay for the screening and

230 , PCR, or culture or positive results by two enzyme-linked immunosorbent assays for cases presenting

231 fluopyram were developed in two alternative enzyme-linked immunosorbent assay formats, using homolog

232 ry examination phase were processed using an enzyme-linked immunosorbent assay from a single batch.

233 Its performance is comparable to enzyme-linked immunosorbent assay from the studies on cl

234 brane antigen (FAMA) assays and glycoprotein enzyme-linked immunosorbent assays (gpELISAs) were used

235 rse transcription-PCR (rRT-PCR), IgM capture enzyme-linked immunosorbent assays (IgM-ELISAs), and inh

236 fluorescence-activated cell sorting (FACS), enzyme-linked immunosorbent assay, immunofluorescence (I

237 s-reactivity to VAR2CSA was characterized by enzyme-linked immunosorbent assay, immunofluorescence as

238 rse-transcription polymerase chain reaction, enzyme-linked immunosorbent assay, immunofluorescence, a

239 Using enzyme-linked immunosorbent assay, immunohistochemistry,

240 GAP-43 was measured using an enzyme-linked immunosorbent assay in 105 MS patients (73

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

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

243 IgA, and IgG) to these antigens by means of enzyme-linked immunosorbent assay in patients with suspe

244 roup box 1 protein levels were analyzed with enzyme-linked immunosorbent assay in repeated samples.

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

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

247 Using these antibodies, a sandwich enzyme-linked immunosorbent assay (LAM-ELISA) was develo

248 Using enzyme-linked immunosorbent assays, levels of antibody r

249 plied the CID system to a sensitive sandwich enzyme-linked immunosorbent assay-like assay of cannabid

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

251 dard immunoglobulin M (IgM) antibody-capture enzyme-linked immunosorbent assay (MAC-ELISA).

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

253 althy individuals was highly correlated with enzyme-linked immunosorbent assay measurements; moreover

254 mated in peri-implant crevicular fluid using enzyme-linked immunosorbent assay method and assessed wi

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

256 ere independently validated using Luminex or enzyme-linked immunosorbent assay methods.

257 G-Abs) were first detected by immunoblot and enzyme-linked immunosorbent assay nearly 30 years ago, b

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

259 objective was to evaluate the application of enzyme-linked immunosorbent assay optical density thresh

260 rm a sensitivity and specificity analysis of enzyme-linked immunosorbent assay optical density thresh

261 tudy was to evaluate the applicability of an enzyme-linked immunosorbent assay optical density thresh

262 e characterization of monoclonal antibodies (enzyme-linked immunosorbent assay, or "ELISA"), to small

263 These proteins were immobilized on enzyme-linked immunosorbent assay plates in their native

264 erotonin release assay, and immunoglobulin G enzyme-linked immunosorbent assay positive) and serotoni

265 olymerase chain reaction (messenger RNA) and enzyme-linked immunosorbent assay (protein).

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

267 n quantitative polymerase chain reaction and enzyme-linked immunosorbent assays, respectively.

268 Enzyme-linked immunosorbent assay revealed that the form

269 ice were analyzed using HEV antigen-specific enzyme-linked immunosorbent assay, reverse transcription

270 roduction was measured using flow cytometry, enzyme-linked immunosorbent assay, RNA in situ hybridiza

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

272 onal and monoclonal antibodies by inhibition enzyme-linked immunosorbent assay, surface plasmon reson

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

274 eceptor (CD206) and tumor necrosis factor by enzyme-linked immunosorbent assay (test cohort).

275 chain reaction (RT-PCR) and immunoglobulin M enzyme-linked immunosorbent assay testing to detect ZIKV

276 tients were tested with the immunoglobulin G enzyme-linked immunosorbent assay, the serotonin release

277 alizing antibody [PRNT80 titers, 40-640] and enzyme-linked immunosorbent assay titers) after the boos

278 We developed an enzyme-linked immunosorbent assay to measure anti-DENV N

279 We used an enzyme-linked immunosorbent assay to measure levels of s

280 healthy controls (CON, n = 14), we utilized enzyme-linked immunosorbent assay to measure NFL and pro

281 flow assays (LFAs) and two laboratory-based enzyme-linked immunosorbent assays to detect anti-SARS-C

282 By co-immunoprecipitation and enzyme-linked immunosorbent assay using recombinant prot

283 more, we analyzed galectin-9 serum levels by enzyme-linked immunosorbent assay using serum samples fr

284 We also performed enzyme-linked immunosorbent assays using a recombinant w

285 Capture enzyme-linked immunosorbent assays using specific rabbit

286 An in-house enzyme-linked immunosorbent assay utilizing recombinant

287 A VP2-peptide enzyme-linked immunosorbent assay (VP2-ELISA) was optimi

288 Enzyme-linked immunosorbent assay was used to assess lev

289 Enzyme-linked immunosorbent assay was used to determine

290 Enzyme-linked immunosorbent assay was used to determine

291 Enzyme-linked immunosorbent assay was used to determine

292 he presence of anti-Cas9 antibodies using an enzyme-linked immunosorbent assay, we detected antibodie

293 t antigens of Bexsero, and Western blots and enzyme-linked immunosorbent assays were used to assess t

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

295 rum anti-CFA/I total antibodies, detected by enzyme-linked immunosorbent assay, were the best predict

296 les, in various immunoassay formats, such as enzyme-linked immunosorbent assay, Western blot, and lat

297 Conventional techniques such as the enzyme-linked immunosorbent assay, Western Blot, and mas

298 rming a paper-based HIV-1 p24 capsid protein enzyme-linked immunosorbent assay, which achieved a reco

299 Comparative enzyme-linked immunosorbent assays with monoclonal antib

300 InBios ZIKV Detect 2.0 IgM antibody capture enzyme-linked immunosorbent assay (ZIKV 2.0 MAC-ELISA; I