ライフサイエンスコーパス: enzyme-linked

1 The approach (referred to as enzyme-linked aptamer kissing complex assay (ELAKCA)) re

2 We report herein a novel sandwich-type enzyme-linked assay for the "signal-on" colorimetric det

3 g the electrochemical readout of up to eight enzyme-linked assays (ELAs), simultaneously.

4 mance to commercially produced antibodies in enzyme-linked competitive assays.

5 boratories, in particular the class based on Enzyme Linked Fluorescent Assays (ELFA) takes advantage

6 nd alphavbeta3 affinities were determined in enzyme linked immune sorbent assay on immobilized integr

7 e focus on transferring a complete IFN-gamma enzyme-linked immune-sorbent assay (ELISA) onto a commer

8 C), purified and the quality was assessed by enzyme linked immuno sorbet assay.

9 which is faster, and as sensitive as current enzyme-linked immuno-assays for cTnI.

10 correlation between patient serum assays and enzyme-linked immuno-sorbent assays (ELISA).

11 avidity assay by modifying the Ortho 3.0 HCV enzyme-linked immunoassay and tested 997 serum or plasma

12 uorescent microbead-based immunoassay and/or enzyme-linked immunoassay platform to characterize the a

13 ar MUC5AC concentration was quantified using enzyme-linked immunoassay, and conjunctival goblet cell

14 e changes validated by mass spectrometry and enzyme-linked immunoassay.

15 transcription polymerase chain reaction, and enzyme-linked immunoassay.

16 ese devices have been used to perform simple enzyme linked immunoassays on paper.

17 Results are validated by enzyme-linked immunoassays of the sera in a certified la

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 Enzyme-linked immunosorbent assay (ELISA) demonstrates m

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

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

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

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

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

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

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

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

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

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

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

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

51 Enzyme-linked immunosorbent assay (ELISA) measurements o

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

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

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

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

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

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

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

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

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

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

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

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

64 90%) was found in 5 tests only: polyspecific enzyme-linked immunosorbent assay (ELISA) with intermedi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 By enzyme-linked immunosorbent assay and immunofluorescence

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 We used enzyme-linked immunosorbent assay to measure endogenous

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

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

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

145 Enzyme-linked immunosorbent assay was used to determine

146 Enzyme-linked immunosorbent assay was used to measure ch

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

255 6, and TNF-alpha levels were estimated using enzyme-linked immunosorbent assays in GCF and serum samp

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

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

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

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

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

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

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

263 Comparative enzyme-linked immunosorbent assays with monoclonal antib

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

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

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

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

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

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

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

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

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

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

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

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

276 d, Ag-specific interleukin-4 (IL-4) T-helper enzyme-linked immunosorbent spot (ELISpot) assays of the

277 vitro assays of interferon gamma production (enzyme-linked immunosorbent spot [ELISPOT] assays) by sp

278 gan Response Test (kSORT), and the IFN-gamma enzyme-linked immunosorbent spot assay (ELISPOT) assay w

279 ter transplant using the Quantiferon-CMV, an enzyme-linked immunosorbent spot assay (ELISpot), and in

280 2Delta30 and used them in a gamma interferon enzyme-linked immunosorbent spot assay to interrogate CD

281 ewly established guinea pig gamma interferon enzyme-linked immunosorbent spot assay.

282 tricted epitope using interferon (IFN)-gamma enzyme-linked immunospot (ELISPOT) and intracellular cyt

283 tive allo-HCT recipients with a CMV-specific enzyme-linked immunospot (ELISPOT) assay and for CMV inf

284 rs with the same peptide pools in a cultured enzyme-linked immunospot (ELISPOT) assay.

285 ysaccharide cellular immunity, measured with enzyme-linked immunospot (ELISPOT) interferon gamma rele

286 r tissues and analyzed by flow cytometry and enzyme-linked ImmunoSpot (ELISpot).

287 sorbent assay (gpELISA) and interferon-gamma enzyme-linked immunospot (IFN-gamma ELISPOT), blood samp

288 nd assessed HBV-specific T-cell responses by enzyme-linked immunospot and cytometric bead array.

289 ain SCC-derived antigens using the IFN-gamma enzyme-linked immunospot assay and intratumor (IT) and c

290 validation cohort were measured by IFN-gamma enzyme-linked immunospot assay or intracellular cytokine

291 Viral loads, CD4(+) T-cell counts, and enzyme-linked immunospot assay-determined anti-HIV-1 CD8

292 us peptides via interferon-gamma (IFN-gamma) enzyme-linked immunospot assay.

293 Interferon gamma (IFN-gamma) enzyme-linked immunospot assays were performed before an

294 s, trans-vivo delayed-type hypersensitivity, enzyme-linked immunospot assays, the use of antigen rece

295 ukin 2, 4, 5, and 6 were counted by means of enzyme-linked immunospot, and SFC counts were compared b

296 Enzyme-linked immunospots, cytotoxicity assays as well a

297 re active 6PGDH mutants were examined via an enzyme-linked TNBT-PMS colorimetric assay.

298 in specific lipid classes and pathways, and enzymes linked to them display signatures of greater sta

299 y, and results were compared to those of the enzyme-linked virus-inducible system (ELVIS) as the refe

300 upregulation of heme oxygenase 1 (HO-1), an enzyme linked with suppression of inflammatory responses