ライフサイエンスコーパス: scintillation

1 eads to light emission in a process known as scintillation.

2 s with brighter, faster, and more controlled scintillation.

3 adioluminescence, Cerenkov luminescence, and scintillation.

4 Column effluents were quantified by liquid scintillation.

5 iquid scintillation counting (LSC) or liquid scintillation analysis (LSA) method, though widely used

6 eactor bioshield using combustion and liquid scintillation analysis has identified two forms of (3)H,

7 is solution were counted in a Packard liquid scintillation analyzer; the mean radioactivity in becque

8 support this conclusion, while highlighting scintillation as a useful tool in our understanding of F

9 Scintillation based X-ray detection has received great a

10 Scintillation-based fiber dosimeters are a powerful tool

11 bind and excite the streptavidin-conjugated scintillation beads.

12 tion, but while the subject was experiencing scintillations, BOLD signal followed the retinotopic pro

13 tical axis in front of a stationary clinical scintillation camera equipped with a pinhole collimator.

14 ction of a dual-head variable-angle-geometry scintillation camera equipped with thicker crystals (5/8

15 Scintillation camera images contain a large amount of Po

16 A-IgG were co-injected into six subjects and scintillation camera images were acquired at 6 and 18 hr

17 ritumomab tiuxetan and assessed using planar scintillation camera imaging at 5 time points and CT-org

18 ed patient data available from a combined CT-scintillation camera imaging system.

19 ssessed by the imaging of animals on a gamma-scintillation camera using quantitative region-of-intere

20 total 67Cu photopeak counts detected with a scintillation camera were attributable to 64Cu.

21 ement techniques involving imaging by planar scintillation camera, SPECT and PET for the calculation

22 anted kidneys were obtained with a dual-head scintillation camera.

23 d radiation dose (TSARD) was determined from scintillation-camera conjugate views, and the tumor volu

24 Scintillation-camera imaging showed that tumor xenograft

25 ively fast and can be used to produce liquid scintillation cocktails e.g., via benzene synthesis.

26 es with good sensitivity, without the use of scintillation cocktails.

27 instead of detection of activity by a liquid scintillation counter (LSC), the compounds can be quanti

28 e spent all at once, plus an ancient Packard scintillation counter that had a series of rapidly flash

29 shed, and the radioactivity is measured in a scintillation counter.

30 ange of protons on glycine, which requires a scintillation counter.

31 canning of the TLC plate or by counting in a scintillation counter.

32 eceptor-bound radioactivity is detected in a scintillation counter.

33 ss [32P]PPi and then measuring [32P]ATP in a scintillation counter.

34 the supernatant, which is then counted in a scintillation counter; a linear increase in the release

35 Events are selected by requiring hits on scintillation counters mounted in the forward region of

36 Samples are counted for (35)S using liquid scintillation counting (LSC) and for (22)Na via y spectr

37 r elution, (99)Tc is detected using a liquid scintillation counting (LSC) detector.

38 specific elapsed time intervals using liquid scintillation counting (LSC) for nanomolar concentration

39 The liquid scintillation counting (LSC) or liquid scintillation ana

40 of SO4 can be analyzed using current liquid scintillation counting (LSC) techniques.

41 has been directly compared to that of liquid scintillation counting (LSC).

42 ccelerator mass spectrometry (AMS) or liquid scintillation counting (LSC).

43 and offline radiometric detection by liquid scintillation counting (LSC).

44 and ocular tissues were quantified by liquid scintillation counting (LSC).

45 r, both as FeSO4, was measured by whole-body scintillation counting 13 d after oral administration.

46 ed with X-ray film and quantitated by liquid scintillation counting after extraction from the gels.

47 into the proteins, was quantitated by liquid scintillation counting after gel solubilization by H2O2.

48 Labelled peptides were detected by on-line scintillation counting after immunoprecipitation and HPL

49 bel into the fusion proteins was measured by scintillation counting after sodium dodecyl sulfate-poly

50 at five time points in tissue extracts using scintillation counting and 13C nuclear magnetic resonanc

51 olabeled chemical in conjunction with liquid scintillation counting and accelerator mass spectrometry

52 in food samples using ultra low-level liquid scintillation counting and alpha-particle spectrometry.

53 times after injection and subjected to gamma-scintillation counting and autoradiography (ARG).

54 , P<0.05 in spleen), corroborated by ex vivo scintillation counting and autoradiography.

55 1.3+/-0.03; P<0.05), corroborated by ex vivo scintillation counting and autoradiography.

56 By combining liquid scintillation counting and ex vivo dual-isotope radio-im

57 (1, 3, 7, 14, and 35 days) were analyzed by scintillation counting and HPLC to characterize the phar

58 on by mixed, undefined cultures using liquid scintillation counting and liquid chromatography with ra

59 both control and ARF rats, as detected using scintillation counting and whole-body ARG (10.56 +/- 1.0

60 ed by quantitative autoradiography and gamma-scintillation counting at 24 h after CED, 47.4% of the i

61 n from vinegar used in preparation of liquid scintillation counting cocktails for measurements of low

62 Autoradiography and scintillation counting confirmed the in vivo findings.

63 Ex vivo gamma-scintillation counting corrected for sham-operated nonsp

64 radiolabeled receptor-antibody complexes and scintillation counting enabled quantitation of the subty

65 tric approach using industry-standard liquid scintillation counting equipment that can both identify

66 wet chemistry digestion technique and liquid scintillation counting for (14)C activity measurements.

67 zed with this overall approach and by liquid scintillation counting for comparison.

68 ed using (11)C-erlotinib imaging and ex vivo scintillation counting in knockout and WT mice.

69 Whole-gut lavage and whole-body scintillation counting methods were applied to determine

70 intigraphically and measured distribution by scintillation counting of dissected tissues.

71 Material balance was measured by liquid scintillation counting of the starting samples, by LC/ra

72 , and the supernatant was measured by liquid scintillation counting prior to injection on the HPLC to

73 with a flow scintillator analyzer and liquid scintillation counting techniques allows to differentiat

74 The routine application of liquid scintillation counting to (41)Ca determination has been

75 as empirically determined by HPLC and liquid scintillation counting to be 24.4 Ci/mmol, approximately

76 tometrically, and cathepsin D (CD) by liquid scintillation counting using [14C] hemoglobin as substra

77 merit similar to those obtained with liquid scintillation counting were achieved by exploiting a sim

78 amples with 3H activities measured by liquid scintillation counting were utilized to develop and vali

79 uantified using both MALDI-TOF-MS and liquid scintillation counting with (3)H-TPP.

80 se vial were calibrated using 4pibeta liquid scintillation counting with 3H-standard efficiency traci

81 h replaces the traditional radiolabeling and scintillation counting with fluorescent staining and dig

82 opriate region of the gel followed by liquid scintillation counting yields an isotope ratio which ref

83 in-agarose beads) and quantitative analysis (scintillation counting) of only the biotinylated glycope

84 as isolated, purified and analyzed by liquid scintillation counting, (2)H- or (13)C NMR or selective

85 ioisotope incubations coupled with NanoSIMS, scintillation counting, and isotope ratio mass spectrome

86 d couples solid phase extraction with liquid scintillation counting, and scintillating anion exchange

87 The radioactivity was measured by scintillation counting, and the absolute disintegrations

88 values, measured experimentally using liquid scintillation counting, fit very well the expected value

89 aphy-mass spectrometry, (13)C- and (1)H-NMR, scintillation counting, HPLC, gas chromatography-flame i

90 Scintillation counting, in particular, provides a signal

91 nstituted enzyme mixture, followed by liquid scintillation counting, indicated that [14C]-8-MOP bindi

92 isolated and analyzed by NMR spectroscopy or scintillation counting, respectively.

93 eins on a glass fiber filter for analysis by scintillation counting, was designed to be fast and accu

94 concentrations in the whole brain by liquid scintillation counting.

95 ing levels of [3H]thymidine incorporation by scintillation counting.

96 ed conjugate present is determined by liquid scintillation counting.

97 try and validated by whole-body potassium-40 scintillation counting.

98 sing radiolabeled substrate, extraction, and scintillation counting.

99 rophoretic separation and autoradiography or scintillation counting.

100 H-thymidine into nuclear DNA as monitored by scintillation counting.

101 ed by quantitative autoradiography and gamma-scintillation counting.

102 and radiolabel incorporation was assayed by scintillation counting.

103 remained at specified times was measured by scintillation counting.

104 ransported protein was quantitated by liquid scintillation counting.

105 substrate and the radioactivity measured by scintillation counting.

106 portions of lenses were determined by liquid scintillation counting.

107 aper and the radioactivity was determined by scintillation counting.

108 ts were quantified by metabolic labeling and scintillation counting.

109 radiometric measurement of trapped 14CO2 by scintillation counting.

110 labeled products and their identification by scintillation counting.

111 cid precipitation of the protein followed by scintillation counting.

112 ed by quantitative autoradiography, TLC, and scintillation counting.

113 n each sample is less than that required for scintillation counting.

114 unoprecipitation by HPLC with on-line liquid scintillation counting.

115 ody scintigraphy, autoradiography, and gamma scintillation counting.

116 hy, the 3H activity was determined by liquid scintillation counting.

117 tography (HPLC) with detection by continuous scintillation counting.

118 abeled DNA to the bead-immobilized enzyme by scintillation counting.

119 raphy and quantified in protocorms by liquid scintillation counting.

120 pproach with radiolabel detection via liquid scintillation counting.

121 ctivity concentration was measured by liquid scintillation counting.

122 ion of I2 with subsequent analysis by liquid scintillation counting.

123 intravenous administration and up to 48 h by scintillation counting.

124 yer chromatography, and quantified by liquid scintillation counting.

125 cally added (65)Zn and subsequent whole-body scintillation counting.

126 sotope retention was monitored by whole-body scintillation counting.

127 nce liquid chromatography and quantitated by scintillation counting.

128 ioactivity of each fraction is determined by scintillation counting.

129 ers and decorated with SiO(2) containing the scintillation-coupled photosensitizer methylene blue and

130 sists of an 8 x 8 array of 2 x 2 x 10-mm LSO scintillation crystals that are coupled to a 64-channel

131 Highly efficient scintillation crystals with short decay times are indisp

132 rotocol uses solid-phase microextraction and scintillation detection as analytical tools to quantify

133 developed for simultaneous concentration and scintillation detection of technetium-99 in water.

134 free column volume), which is placed into a scintillation detection system to obtain pulse height sp

135 Using a NaI(Tl) scintillation detector designed to operate in electrical

136 Additionally, GaN-based scintillation detector with a (6)LiF neutron conversion

137 This work investigated thermal neutron scintillation detectors composed of GaN thin films with

138 Organic scintillation detectors output pulses that are proportio

139 of a new generation of cryogenic, efficient scintillation detectors with nanosecond response time, m

140 ble with pulse-height in intrinsic GaN-based scintillation detectors.

141 Much higher alpha-scintillation efficiency has been obtained for the (241)

142 oit the difference between the Cherenkov and scintillation emission spectra and use dichroic filters

143 llators that accounts for the key aspects of scintillation: energy loss by high-energy particles, and

144 ging performance and provide a route towards scintillation enhancements without compromising resoluti

145 do not exhibit afterglow and maintain stable scintillation even under high X-ray doses (>10(9 )Gy).

146 Among other realistic simulations of scintillation events in clinical positron-emission tomog

147 mal coating conditions were determined, both scintillation fiber and resin functions were retained, p

148 ed compounds, than conventional SPA beads or scintillation fluid (emitting at 400 to 480 nm region).

149 blished by the addition of a phase partition scintillation fluid (PPSF).

150 The PPSF serves as a scintillation fluid, a phase partition agent, and a carr

151 effects of lensing from these cloudlets and scintillation from plasma screens in the Milky Way inter

152 coronary arteries on in vivo imaging using a scintillation gamma camera.

153 surements have been carried out using liquid scintillation, gamma, alpha and mass spectrometry.

154 Scintillation has widespread applications in medical ima

155 e reported including, notably, intense X-ray scintillation in Cs3TbSi4O10F2.

156 sium rare earth silicates exhibiting intense scintillation in several ranges of the visible spectrum

157 intillation measurements with XRIL, the fast scintillation in ZnO crystals was found to be strongly c

158 tor modes through a turbulent channel with a scintillation index of 1.09, and 4.02 bits per pulse usi

159 even stronger turbulence corresponding to a scintillation index of 1.54.

160 However, the presence of slower scintillation light and the inability of existing detect

161 The vacuum ultraviolet (VUV) scintillation light emitted by these Liquid argon (LAr)

162 charge-coupled-device camera to capture the scintillation light excited by an electron-emitting obje

163 ranging for autonomous driving, detection of scintillation light in ionizing radiation, as well as hi

164 The scintillation light is transmitted to position-sensitive

165 scintillator based detectors that detect the scintillation light on an individual photon basis via an

166 nyltoluene) matrices resulting in comparable scintillation light output and neutron capture as state-

167 pertechnetate detection by the absorption of scintillation light pulses (color quench).

168 An optical light guide transmits the scintillation light to the flat-panel multianode positio

169 The scintillation light yield of CsPbBr(3) at 7 K is assesse

170 MS), alpha spectrometry, Cerenkov and liquid scintillation (LS) counting.

171 tectors to distinguish between Cherenkov and scintillation make it difficult for BGO to achieve a goo

172 Overall, efficient, fast, and durable scintillation make quantum shells appealing in applicati

173 Scintillation materials convert high-energy radiation to

174 ng and argue that positive detections of FRB scintillation may constrain the properties of these cool

175 By combining scintillation measurements with XRIL, the fast scintilla

176 ission (tens of picoseconds) with respect to scintillation (nanosecond).

177 whose interpretation is severely impaired by scintillation noise.

178 es of these cool-gas cloudlets, with current scintillation observation weakly disfavoring the cloudle

179 y of temperature monitoring, using ultrafast scintillation of PbI(2) excited by X-ray pulses from a s

180 th Cerenkov radiation and the gamma and beta scintillation of radionuclides, as well as on their biol

181 hat we can enhance the ratio of Cherenkov to scintillation photons by a factor of 2.17 +/- 0.38 by em

182 ntillation proximity assay (SPA) beads and a scintillation plate counter.

183 (131)I in each body was measured at 2 d by a scintillation probe.

184 External scintillation probes with coincidence detection circuitr

185 Its X-ray scintillation properties are characterized with an excel

186 ponse in the order of ns confirmed promising scintillation properties for fast and high-resolution X-

187 In this work, we report on excellent scintillation properties of CsPbBr(3) crystals when cool

188 XRIL technique for the study of emission and scintillation properties of materials.

189 ra is strongly tied to both the physical and scintillation properties of the crystals.

190 The luminescence and scintillation properties of ZnO single crystals were stu

191 owth and their structural, optical and X-ray scintillation properties were investigated.

192 ) films that exhibit outstanding optical and scintillation properties, with a high photoluminescence

193 d coupling resulting in luminescent and fast scintillation properties.

194 time-resolved fluorescence energy transfer, scintillation proximity and high content analysis micros

195 rmat described is called an aaRS competitive scintillation proximity assay (cSPA).

196 Identified "hits" were then confirmed in a scintillation proximity assay (SPA) and a DEAE membrane-

197 neous proximity assays for tyrosine kinases, scintillation proximity assay (SPA) and homogeneous time

198 e obtained from the conventional assay using scintillation proximity assay (SPA) beads and a scintill

199 By using wheat germ agglutinin (WGA)-coated scintillation proximity assay (SPA) beads to capture 125

200 mer was immobilized onto streptavidin-coated scintillation proximity assay (SPA) beads, and after add

201 We describe the first validated scintillation proximity assay (SPA) binding method for q

202 Here we report the development of a coupled scintillation proximity assay (SPA) for 3 KDMs: KDM1A (L

203 A homogeneous scintillation proximity assay (SPA) for detection of RNA

204 hput, we have developed a novel, homogeneous scintillation proximity assay (SPA) for DGAT.

205 Here, by adapting the scintillation proximity assay (SPA) for direct determina

206 We have developed a novel 96-well plate scintillation proximity assay (SPA) for measuring small

207 A simple, high-throughput scintillation proximity assay (SPA) for parathyroid horm

208 using biotinylated NAD, we have developed a scintillation proximity assay (SPA) for PARP.

209 Here we report a 96-well homogeneous scintillation proximity assay (SPA) for the study of Dna

210 usly identified, with a pIC(50) >= 5.0, in a scintillation proximity assay (SPA) HTS at a lower hit r

211 stone deacetylase assay that is based on the scintillation proximity assay (SPA) principle.

212 fatty acid amide hydrolase (FAAH) using the scintillation proximity assay (SPA) technology is descri

213 , and homogeneous binding assay based on the scintillation proximity assay (SPA) technology that prov

214 o previously reported procedures: the use of scintillation proximity assay (SPA) technology to measur

215 (RPA) with the quantification advantages of scintillation proximity assay (SPA) technology.

216 H2 domain with a phosphopeptide ligand using scintillation proximity assay (SPA) technology.

217 We have developed a quantitative scintillation proximity assay (SPA) that reproduces the

218 We have adapted and optimized a scintillation proximity assay (SPA) to replace the more

219 A scintillation proximity assay (SPA) using 33phosphorous

220 A scintillation proximity assay (SPA) was developed to det

221 tosaminyltransferase (GalNAc-transferase) by scintillation proximity assay (SPA) was developed.

222 We have developed a scintillation proximity assay (SPA) where use of biotiny

223 de triphosphatase activity was measured in a scintillation proximity assay (SPA)-based high-throughpu

224 metal ion affinity chromatography (IMAC) and scintillation proximity assay (SPA).

225 ter-binding format or by a novel homogeneous scintillation proximity assay (SPA).

226 es than on DNA-core-trimmed nucleosomes in a scintillation proximity assay (SPA).

227 In combination with the scintillation proximity assay (SPA[trade]), this allows

228 e use of AMP-PCP coupled with the use of the scintillation proximity assay allows this characterizati

229 high-throughput screening, are described: a scintillation proximity assay and a time-resolved fluore

230 cts by immobilization on streptavidin-coated scintillation proximity assay beads.

231 method described here is the first reported scintillation proximity assay for a peroxisome prolifera

232 A scintillation proximity assay for measurement of 3H-radi

233 A scintillation proximity assay for peroxisome proliferato

234 (50) values obtained by FP binding assay and scintillation proximity assay for the clinically used PP

235 assay for acetyl CoA carboxylase (ACC) in a scintillation proximity assay format suitable for high-t

236 To our knowledge this ACC/FAS coupled scintillation proximity assay is the only assay format t

237 PAR ligands obtained in FP binding assay and scintillation proximity assay or gel filtration binding

238 d the purified DII S1-S4 protein to create a scintillation proximity assay suitable for high-throughp

239 roduct is then directly quantified using the scintillation proximity assay technology: binding of the

240 distinct inhibitory profile, we developed a scintillation proximity assay that permits analysis of r

241 The screen uses a scintillation proximity assay to identify compounds that

242 The soluble receptor was used in a scintillation proximity assay to identify two chemical c

243 We now describe a scintillation proximity assay to measure soluble inosito

244 try of the targeting process, we developed a scintillation proximity assay to study the stepwise asso

245 format for the detection of inhibition is a scintillation proximity assay which is robust and reprod

246 Using the antibody-capture [(35)S]GTPgammaS scintillation proximity assay, we demonstrated for the f

247 ified biochemically with a cytosol-dependent scintillation proximity assay.

248 y were determined using this FP method and a scintillation proximity assay.

249 rsible loss of ligand binding as assessed by scintillation proximity assay.

250 rs of human DNA topoisomerase I based on the scintillation proximity assay.

251 (3)H]troglitazone, a PPARgamma agonist, in a scintillation proximity assay.

252 We developed scintillation proximity assays (SPA) to discover compoun

253 Scintillation proximity assays designed to look at the b

254 ration calorimetry, equilibrium dialysis and scintillation proximity assays.

255 nding and peptide-myristoylation activity in scintillation proximity assays.

256 SH2 domains was monitored utilizing a novel scintillation proximity based assay.

257 anded nucleic acid complex on the surface of scintillation proximity beads derivatized with streptavi

258 d RNA can be captured on streptavidin-coated scintillation proximity beads.

259 A novel scintillation proximity competitive hybridization assay

260 cts radioactive S1P adhering to the plate by scintillation proximity counting.

261 A novel scintillation proximity high throughput assay (SPA) to i

262 d, the final product, is readily detected by scintillation proximity in a FlashPlate or Image FlashPl

263 ) 384-well format using a modified published scintillation proximity method.

264 upled device (CCD) camera and newly designed scintillation proximity microparticles.

265 Scintillation proximity offers an equilibrium method for

266 bined with site-directed mutagenesis and the scintillation proximity radioligand binding assay improv

267 cally by monitoring ligase-AMP formation via scintillation proximity technologies.

268 ing a ligand binding assay that incorporates scintillation proximity technology to circumvent many of

269 96-well membrane plate assay and a 384-well scintillation proximity-based assay developed herein.

270 Here, we describe a direct scintillation proximity-based radioligand-binding assay

271 The molecule exhibits activity in a scintillation-proximity assay for the inhibition of the

272 We have developed a cell-free and scintillation-proximity assay-based screen to search for

273 cant interference from beta particles in the scintillation pulse height spectra of Pu.

274 oactive decay of Tc-99 results in detectable scintillation pulses that are counted in coincidence.

275 Finally, HPLC scintillation quantification of (3)H-myo-inositol labele

276 damentally different approach: enhancing the scintillation rate and yield via the Purcell effect, uti

277 chroic filters to enhance the Cherenkov over scintillation ratio.

278 lead iodide exhibits a very fast and intense scintillation response due to excitons and donor-accepto

279 The scintillation response of poly(ethersulfone)-based membr

280 The scintillation results presented in this work independent

281 ent the measurement of two mutually coherent scintillation scales in the frequency spectrum of FRB 20

282 loying a NPs containing flexible film as the scintillation screen, the inside 3D electrical structure

283 The scintillation sensor could be successfully tested for Pu

284 resent study focuses on the development of a scintillation sensor specifically designed for the selec

285 aximizing the collection and coupling of the scintillation signal into the POF.

286 gas proportional counting (LLGPC) and liquid scintillation spectrometry (LSS).

287 n seawater by way of state-of-the-art liquid scintillation spectrometry.

288 sed and the radioactivity measured by liquid scintillation spectrometry.

289 sed and the radioactivity measured by liquid scintillation spectrometry.

290 gh pressure liquid chromatography (HPLC) and scintillation spectrometry.

291 3521 were assayed by both radiolabel (liquid scintillation spectroscopy) and CGE methods.

292 ivity (by [(14)C]-5-HT metabolism and liquid scintillation spectroscopy) were measured in human neuro

293 The burst scintillation suggests weak turbulence in the ionized in

294 Using a novel miniaturized light-scintillation technique, we quantified a strong retrogra

295 who had any of the following: D-dimer, CTPA, scintillation ventilation perfusion lung scanning or for

296 ed protein products are eluted directly into scintillation vials and counted.

297 mples the assay can be conducted entirely in scintillation vials and quantitated by addition of appro

298 The decay kinetics of the scintillations was measured over the 8-107 K temperature

299 rol (N = 10), identified both by imaging and scintillation well counting.

300 scintillator, demonstrating Purcell-enhanced scintillation with 50% enhancement in emission rate and