ライフサイエンスコーパス: SPR

1 emonstrated using surface plasmon resonance (SPR).

2 rug-target residence time was determined via SPR.

3 nding properties using NMR, SAXS, cryoEM and SPR.

4 erihelion passage during Northern hemisphere spring.

5 ble region potentially acting as a molecular spring.

6 ave breaking events during boreal winter and spring.

7 ed in canopies of orchard trees during early spring.

8 e-scale climate patterns during the previous spring.

9 has finite mass and is attached to a linear spring.

10 ified SST and SLP patterns from the previous spring.

11 nt of cold-sensitive floral organs until the spring.

12 onse to winter cold to initiate flowering in spring.

13 and then dramatically increased by 83.4% in spring.

14 s promoted by increasing temperatures during spring.

15 at low postvernalisation temperatures in the spring.

16 are major cues determining flowering time in spring.

17 A) pattern--is predictable from the previous spring.

18 dynamics during the transition from fall to spring.

19 ients with symptom debut in the winter/early spring.

20 primarily driven by enhanced C uptake during spring (129%, P = 0.001) and fall (124%, P = 0.001), res

21 During spring 2015, we flew fixed-wing UAS equipped with therma

22 ubtype, A(H3N2), was detected in Illinois in spring 2015.

23 ntal stages and two seasons (autumn 2015 and spring 2016) on the commercial and functional quality (c

24 As of spring 2017, the International Reference Laboratory of M

25 esulted in smaller colonies in the following spring (24% declines).

26 In years with anomalously high spring air temperatures, elderberry fruited several week

27 ony-forming units/capsule) or placebo during spring allergy season for 8 wk.

28 cession postpones flower induction until the spring, allowing plants to avoid winter injuries of flow

29 es and proteins, which are not detectable by SPR alone.

30 X-ray crystallography, HDX-MS and SPR analysis confirmed that the CDR regions of VHH6 inte

31 Notably, SPR analysis indicated that constitution of WTA determin

32 e of immune-reactive biochips and during the SPR analysis.

33 peptides were screened in hydrolysates using SPR and a correlation was established between affinity c

34 at our NanoBioAnalytical platform, combining SPR and AFM, is a suitable method for a sensitive, repro

35 ity molecular target, which was confirmed by SPR and crystallography.

36 shed between affinity constant determined in SPR and metal chelation capacity determined from UV-visi

37 n simplifies the conventional combination of SPR and QCM and has the potential to be miniaturized for

38 sis techniques: the biosensing capability of SPR and the chemical identification power of high resolu

39 nsor, determined here using a combination of SPR and X-ray photoelectron spectroscopy (XPS) measureme

40 In most species, mean spring and autumn migration dates changed little.

41 Spring and autumn migration phenologies were not consist

42 advancement, temporal stability and delay in spring and autumn migration phenologies, altering specie

43 he degree to which the full distributions of spring and autumn migration timing of 13 species of long

44 During spring and autumn migration, species are projected to en

45 considered seasonally paired events spanning spring and autumn or tested the key assumption that sing

46 large westerly detours in Africa on both the spring and autumn routes.

47 During warmer spring and autumn, GSstart is advanced and GSend delayed

48 overwintering grazers, releasing algae from spring and early summer grazing.

49 1st century, modeled GPP mainly increases in spring and fall due to reduced temperature limitation, b

50 over the past century, and report trends in spring and fall frost timing that could stem from hemisp

51 2.5 mum collected in Athens, Georgia, in the spring and fall of 2016, including samples from nearby w

52 s occur and smaller contributions during the spring and fall when prescribed and agricultural fires r

53 eric circulations that account for 25-48% of spring and fall-frost timing.

54 jected to increase in the southern plains in spring and in the central plains in summer, whereas curr

55 neck events and/or selective sweeps within a spring and low migration between springs shape these pop

56 ovements, while their movements north in the spring and south in fall were frequently aided by ice mo

57 decreases are particularly pronounced in the spring and summer in the Gulf of Maine and Georges Bank.

58 collected more frequently during biological spring and summer; specimens of threatened species colle

59 an annual crop, cultivated in the winter and spring and susceptible to several pathogens, especially

60 mpact of emissions, especially for annual or spring and winter precipitation.

61 riptional responses in crowns of field-grown spring and winter wheat (Triticum aestivum) genotypes an

62 p, seasonal shifts in community formed cool (spring and winter) and warm (summer and autumn) subgroup

63 f two ecotypes of S. pruinosus, red-fleshed (SpR) and orange-fleshed (SpO), and two of S. stellatus,

64 crobalance (QCM), surface plasmon resonance (SPR) and X-ray photoelectron spectroscopy (XPS).

65 microscopy (AFM), surface plasmon resonance (SPR), and molecular simulations were used to investigate

66 accelerating the pre-melting process in the spring, and in turn triggered the positive sea-ice albed

67 hip to become four times as sensitive to the SPR angle shift and to have the lowest antibody detectio

68 With respect to the shifts of the SPR angles of the chips, the affinity immunoassay intera

69 Up to present, SPR application in stem cell biology and biomedical scie

70 We demonstrate sPREs as a practical, widely applicable, robust, and ver

71 eus hemionus), 31% surfed plant phenology in spring as well as a theoretically perfect surfer, and 98

72 eptide-spot array screening, competition and SPR assays, high-resolution crystallography, and mutatio

73 tion systems like Surface Plasmon Resonance (SPR) assays, Impedance-based method, Quartz Crystal Micr

74 he characteristic surface plasmon resonance (SPR) band of Tyr-Au NPs was red-shifted to 596 and 616nm

75 A natural mutation in Ppd-H1 prevalent in spring barley delayed floral development and reduced the

76 pha-tocopherol and beta-tocotrienol, whereas spring barley varieties differed from wheat and tritorde

77 heoretical and experimental realization of a SPR based fiber optic nicotine sensor having coatings of

78 id cost-effective surface plasmon resonance (SPR) based method for measuring the Rexocytosis for popu

79 films for use in surface plasmon resonance (SPR)-based immunoaffinity biosensors.

80 ochemical, fluorescence-based, nanomonitors, SPR-based, and field-effect transistor biosensors for ea

81 s were administered during 10th grade in the spring (baseline) and 11th grade in the fall (6-month fo

82 , and show unique surface plasmon resonance (SPR) behaviors.

83 Overall, our work extends the application of SPR beyond the realm of 1:1 stoichiometric ligand-recept

84 The established point-of-care (POC) FO-SPR bioassay was also used to measure IFX in 100-fold di

85 In addition, the nonlinear HCR based SPR biosensing methodology is extended to the detection

86 e and enzyme-free surface plasmon resonance (SPR) biosensing strategy has been developed for highly s

87 clusion, this paper demonstrates that our FO-SPR biosensor can be used as a true POC diagnostic tool

88 or POC, this is the first report of using an SPR biosensor for measuring DBS samples.

89 The VP1 detection in the portable SPR biosensor had a detection limit of approximately 4.8

90 a fiber-optic surface plasmon resonance (FO-SPR) biosensor for detection of IFX spiked in 100-fold d

91 have presented a surface plasmon resonance (SPR) biosensor technique for the detection of anti-PEG a

92 determined using surface plasmon resonance (SPR) biosensor technology are 262 +/- 4 nM for iMVP/INT,

93 GO-peptide-based surface plasmon resonance (SPR) biosensor.

94 Surface plasmon resonance (SPR)-biosensor experiments show that the drug can displa

95 eports the operation principles for reusable SPR biosensors utilizing nanoscale-specific electrostati

96 Surface plasmon resonance (SPR) biosensors are most commonly applied for real-time

97 The timing of the annual phytoplankton spring bloom is likely to be altered in response to clim

98 t that, if pinpointing the start date of the spring bloom is the priority, the highest possible tempo

99 tlantic is characterized by diatom-dominated spring blooms that results in significant transfer of ca

100 e inferred sBC* shows that Asian outflows in spring bring much more BC aerosols to the mid-Pacific th

101 Braincases then partially regrew in spring by 9.3%.

102 onstrating that a surface plasmon resonance (SPR) can be excited in this case.

103 d through pi-stacking on the graphene coated SPR chip and the FAP analyte in serum.

104 O-COOH chip, an Au/GO chip and a traditional SPR chip are 35.5m degrees , 9.128m degrees and 8.816m d

105 ggest the potential of this GO-peptide-based SPR chip detection method in clinical application.

106 o construct a highly sensitive and selective SPR chip for folate biomarker sensing in serum.

107 enzoic acid (4-MBA) modified gold (4-MBA/Au) SPR chip was developed first time for the detection of B

108 nsitivity of 16 times that of a conventional SPR chip.

109 ed by up to 1.2 times that of a conventional SPR chip.

110 olic acid protein (FAP) using graphene-based SPR chips.

111 86I (Kd(app) = 0.2-0.5 mum, as determined by SPR) compared with the lowest-affinity double-alanine pe

112 k was related to season, with higher risk in spring conceptions and lower risk in autumn conceptions,

113 Simulated spring conditions promoted allocation of carbohydrates f

114 ind that over time and in response to warmer spring conditions, short-distance migrants have advanced

115 the external electric field and reducing the spring constant of a cantilever.

116 e to large tensions governed by an effective spring constant that scales with radius as R(-0.25).

117 on sensitivity and subsequently cantilever's spring constant were the main sources of error.

118 the correct deflection sensitivity based on spring constants determined with a vibrometer.

119 ice (Ksp-Cre PKD1 (flox/flox)) and rats (Han:SPRD Cy/+), demonstrating obvious tubular cell morpholog

120 d and applied a novel mathematical model for SPR data treatment that enables determination of kinetic

121 ate influenced access to littoral regions in spring (data from telemetry), which in turn influenced e

122 However, individual spring departure and arrival dates were not related to w

123 lity, the observed between-year variation of spring departure dates was still sufficient for the adva

124 Spring departure timing exhibited high repeatability at

125 was still sufficient for the advancement of spring departure timing.

126 Pelican spring departures and arrivals advanced steadily from 20

127 reat Plains, less dusty days are expected in spring due to increased precipitation and reduced barene

128 man spectroscopy, surface plasmon resonance (SPR), electrochemiluminescence and colorimetric readouts

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

130 A modern spring elite variety, "Paragon," was used as common refe

131 face snowmelt runoff destabilize smaller hot spring environments with smaller populations and result

132 Following Titan's 2009 northern spring equinox, peak solar heating moved to the northern

133 s interpretation, co-immunoprecipitation and SPR experiments indicated that EBI3 binds IL-6.

134 Simulations and SPR experiments suggested that an Fn conformational chan

135 ral life-history strategies, including early spring flight season and brood parasitism, which may ind

136 on of high-value foraging habitat, including spring floral resources, within 250-1,000 m of the natal

137 seasonal variation in C. hirsuta, such that spring flowering plants developed more petals than those

138 Conditions associated with spring flowering, including cool ambient temperature, sh

139 o SN and DNE, and recessive ppd mutants on a spring-flowering hr mutant background show early, photop

140 e a generation of surface plasmon resonance (SPR) for plasmonic sensing.

141 that measured by surface plasmon resonance (SPR) for the same binding reaction.

142 hydrolysate using Surface Plasmon Resonance (SPR) for their antioxidant properties.

143 ibutions of soluble plant protein during the Spring freshet.

144 HR increased for 12 weeks in spring, from minimal hibernation levels (mean 20-25 beat

145 n important mycotoxin, was captured using an SPR gold chip containing an antifouling layer and monocl

146 migration manifests in response to waves of spring green-up (i.e. green-wave surfing).

147 s of change in phenological interval between spring green-up and migratory arrival for 48 breeding pa

148 Up to now, SPR has been poorly exploited for tau detection by immun

149 FO-SPR has enabled sensitive sensing capabilities in biomed

150 gration times have advanced over time and as spring has become warmer.

151 ss and atmospheric water vapor in winter and spring have caused an extraordinary downward longwave ra

152 We conclude that during the spring, honey bees need access to native hedgerows and w

153 ed floral development in the background of a spring HvVRN1 allele with a deletion in the regulatory i

154 be used with most surface plasmon resonance (SPR) imaging instruments.

155 ified coupling of surface plasmon resonance (SPR) immuno-biosensing with ambient ionization mass spec

156 Finally, the POC FO-SPR immunoassay was validated by using matching serum an

157 Surface plasmon resonance (SPR) immunosensor using 4-mercaptobenzoic acid (4-MBA) m

158 We present approaches for measuring sPREs in practically the entire range of magic angle spi

159 e (-1 to -5 degrees C) frost events in early spring in plants in situ.

160 wet during the growing season (e.g. in early spring in some cases).

161 (MTIV), that was isolated from an acidic hot spring in Yellowstone National Park, USA.

162 Surface Plasmon Resonance (SPR) in combination with different amplification strateg

163 nal parks in the southeast during winter and spring, in the Gulf of Mexico southwards of the Texas an

164 oxide (GO)-coated Surface Plasmon Resonance (SPR) interfaces.

165 Surface Plasmon Resonance (SPR) is a powerful technique for studying 1:1 stoichiome

166 a novel surface plasmon resonance technique (SPR) is developed and used, along with hepatocyte (with

167 Surface plasmon resonance (SPR) is the current standard tool used for label-free ki

168 laser trapping, we directly demonstrate the spring-like elasticity of curling protofilaments.

169 vation of MTs in working myocytes suggests a spring-like function, one that is surprisingly tunable b

170 protofilaments can work efficiently via this spring-like mechanism has been unclear.

171 ated to endurance (e.g., larger limb joints, spring-like plantar arch) in Homo was somewhat mosaic, w

172 se-3 (Caspase-LOV) by exploiting its natural spring-loaded activation mechanism through rational inse

173 by a four-pronged iridium gig that yields a "spring-loaded" norbornadiene-like structure with signifi

174 and application of a general strategy where spring-loaded, strained C-C and C-N bonds react with ami

175 lter Reed Army Institute of Research, Silver Spring, MD, USA, or of 5:1 at Saint Louis University, Sa

176 ommonly only measured variation occurring in spring, measured as the first or mean dates on which foc

177 nstants with literature values and analogous SPR measurements indicates that this approach is applica

178 Transmission SPR measurements of free prostate specific antigen (f-PS

179 perature gradient surface plasmon resonance (SPR) measurements to quantitatively evaluate how the sta

180 sotopes from the snowpack through the entire spring melt runoff period for two years.

181 SPR method can become a valuable addition to analytical

182 the potential of surface plasmon resonance (SPR) method coupled to atomic force microscopy (AFM) to

183 re wide reports of advances in the timing of spring migration of birds over time and in relation to r

184 cological causes of the advancement in avian spring migration phenology is still a challenge due to t

185 Spring migration phenology of birds has advanced under w

186 ssing slope estimates of the timing of avian spring migration regressed on (i) year and (ii) temperat

187 rage birds have significantly advanced their spring migration time by 2.1 days per decade and 1.2 day

188 On average, avian spring migration times have advanced over time and as sp

189 ri-urban, and increased precipitation during spring migration.

190 the wintering grounds would advance pelican spring migration.

191 tions, short-distance migrants have advanced spring migratory phenology by more than long-distance mi

192 et al. show how to map a spin ensemble to a spring model so analytic pulses can be designed using li

193 last 60 years both high-frequency summer and spring NAO, and low-frequency winter NAO components are

194 semi-diurnal gravimetric tides: the 14.8-day spring-neap cycle, the 13.7-day declination cycle and th

195 As actomyosin forces stretch the spring network, simulations predict the resulting tracti

196 t global mechanical properties of disordered spring networks can be tuned by selectively modifying on

197 First documented in the spring of 2010 affecting 24 328 hectares in the state of

198 inland China, with 134 cases reported in the spring of 2013, 306 in 2013-14, 219 in 2014-15, 114 in 2

199 cquired Lassa virus infection in Togo in the spring of 2016 was repatriated to the United States for

200 ransmission is likely to have started in the spring of 2016-several months before its initial detecti

201 which include the surface plasmon resonance (SPR) of Au nanoparticles, low overpotential of Pt nanopa

202 SPR offers several advantages in terms of label free det

203 The SPR partition data obtained for the antibody fragment F6

204 phenologies differed strongly, with an early spring peak followed by decline in forests, and a more e

205 bacteria did not differ in Bd inhibition in spring peeper and toad populations, in which Bd was abse

206 yrus americanus), western toads (A. boreas), spring peepers (Pseudacris crucifer), Pacific treefrogs

207 nus), leopard frogs (Lithobates pipiens) and spring peepers (Pseudacris crucifer)] to examine how pri

208 Mortality following Bd exposure increased in spring peepers and American toads and was dependent upon

209 amphibian species: bullfrogs, Eastern newts, spring peepers and American toads.

210 of the relative abundance was inhibitory on spring peepers and toads, respectively.

211 a from 1983 to 2010 to estimate variation in spring phenology from 280 plant and insect species and t

212 nual variation in bird phenology relative to spring phenology, and related asynchrony to annual avian

213 ties of localized surface plasmon resonance (SPR) phenomenon to study non-covalent interactions not j

214 y between regional and temporal variation in spring polar bear fasting and food web productivity sugg

215 In early spring, pollen diet supplementation accelerated the indu

216 computational procedure to construct a bead-spring polymer model based on the EP matrix.

217 wth at the root collar was best explained by spring precipitation and summer temperature, whereas ste

218 essure, warmer water temperatures, and lower spring precipitation.

219 FO-SPR probes were homogeneously functionalized with ZIF-8

220 olvent paramagnetic relaxation enhancements (sPREs) proved to be a powerful method for probing protei

221 nstrate that (1)H and (15)N relaxation-based sPREs provide a powerful tool for characterizing intermo

222 amily lineages from the summer worker to the spring queen stage in the following year increases signi

223 We find a trend of advanced spring recovery of carbon uptake for this period, with a

224 tivity of the measured springtime GPP to the spring recovery to be in accordance with the correspondi

225 Using a stochastic, bead-spring representation of chromatin in budding yeast, we

226 rimetry (ITC) and surface plasmon resonance (SPR), respectively.

227 hitecture is a typical complex system, where SPR response is formed by the stochastic interactions wi

228 Real-time amplified SPR response is observed upon the introduction of nonlin

229 oin antibodies by surface plasmon resonance (SPR) revealed low nanomolar antiserum affinity for the k

230 en outputs throughout the year except during spring runoff, and also during autumn storms in the catc

231 For spring-sampled adults, THg concentrations declined by 13

232 We used this approach to analyze two hot spring samples from Yellowstone National Park and extrac

233 taken through the early stages of respective spring sea-ice melting at coastal sites in northeast Gre

234 of the Texas and Louisiana coastline during spring season and along the Mississippi River Delta duri

235 Data were collected during the spring semester (January to June) in each survey cycle b

236 The SPR sensor instrument was configured to run on low power

237 A Surface Plasmon Resonance (SPR) sensor chip consisting of four sensing arrays enabl

238 ed ultrasensitive surface plasmon resonance (SPR) sensor in a checkerboard nanostructure on plastic s

239 spectra are recorded simultaneously with the SPR sensorgram, and the detected Raman bands provide che

240 ein, the major advantage of GO-peptide-based SPR sensors was their reduced nonspecific adsorption and

241 The two established MOF-FO-SPR sensors were then subjected to sensing experiments w

242 SPR sensors with different average surface densities of

243 er optic based surface plasmon resonance (FO-SPR) sensors.

244 This SPR shift correlates remarkably well with biochemical es

245 Moreover, surface plasmon resonance (SPR) showed that longer chain of synthetic alpha(1-6)man

246 structures (metallic or not) may amplify the SPR signal and improve the limit of detection to the des

247 bioassay with the capability to increase the SPR signal of about 10(2) folds compared to direct detec

248 The SPR signal processing using integration area under the r

249 for the first time, the presence of a stable SPR signal recorded in soft matters.

250 es, causing a characteristic decrease in the SPR signal.

251 , resulting in a significant increase of the SPR signal.

252 The SPR signals increased with the increase of the amount of

253 efore, physical abiotic features such as hot spring size and position in the landscape are important

254 Warmer temperatures have led to earlier spring snowmelt floods throughout northeastern Europe; d

255 ringtime sum of GPP related to the timing of spring snowmelt is quantified here for boreal evergreen

256 ntified unexpected haplotype sharing between spring-spawning oceanic herring and autumn-spawning popu

257 gut communities during the early winter and spring, specifically a high relative abundance of Synech

258 ll-characterized by pronounced difference in SPR spectral band position (shifting up to 50nm).

259 To address this problem, we use SPR spectroscopy correlated with surface enhanced Raman

260 Surface plasmon resonance (SPR) spectroscopy is an advanced tool to measure binding

261 ographic profile of betalains was similar in SpR, SpO, and SsR, where indicaxanthin, gomphrenin I, ph

262 ement of both the mechanical damping and the spring stiffness, facilitating low-power mechanical cool

263 f SSU rRNA and mcrA transcripts from one hot spring suggested that predominant Bathyarchaeota were al

264 n repeat domain of NOMPC resembles a helical spring, suggesting its role of linking mechanical displa

265 antial reduction of infected colonies in the spring, suggesting that virus-infected individuals had d

266 ovides a simple explanation for not only the spring-summer timing of historical pandemics, but also e

267 ociated with total arsenic or DMA during the spring/summer.

268 hanical systems, such as buckling transition spring switches, can have engineered, stable configurati

269 o solutions was directly monitored by the FO-SPR system.

270 connection between nonlinear spin and linear spring systems and show the surprising result that such

271 the direct and label-free detection with the SPR technique and neutralized chimeric probe DNA can be

272 Intuitively, interannual spring temperature variability (STV) should influence th

273 One consequence of rising spring temperatures is that the optimum timing of key li

274 ratures much more in the wMed (during winter/spring) than in the eMed (during summer).

275 eased in nongrowing season and peaked during spring thaw in each year.

276 nowfall inducing higher soil moisture during spring thaw.

277 variation were photoperiod and the onset of spring, the Julian date of accumulating degree-days >5 d

278 eehives were placed in a screen tent in late spring, thereby artificially suppressing brood-rearing a

279 Finally, we use sPREs to characterize protein-protein interfaces in the

280 t activity in the southern Great Plains from spring to fall in the late half of the twenty-first cent

281 were screened by surface plasmon resonance (SPR) to determine the binding dissociation constant (off

282 try of ecosystems, both during the winter-to-spring transition and throughout the rest of the year.

283 hyll-a was significantly correlated with the Spring Transition Index (STI) that sets biological produ

284 Grip strength was assessed using Smedley spring-type hand dynamometers, and walking speed was ass

285 s implemented for a quantitative analysis of SPR under plane-wave illumination and a finite-differenc

286 applications, which gives rise to the recent spring-up of ionic liquid-based functional materials.

287 nter conditions NA species required 84% more spring warming for bud break, EU ones 49% and EA ones on

288 g requirements in species from regions where spring warming varies greatly among years.

289 Using surface plasmon resonance (SPR), we found that IL-1RAcP also does not bind IL-36R w

290 With surface plasmon resonance (SPR), we present this diversified collection to collagen

291 Spring weather conditions in both countries have a major

292 local trends, with the inclusion of a latent spring weather covariate.

293 IFX concentrations determined with FO-SPR were compared to a clinically validated enzyme-linke

294 lso find that barley, sorghum, winter wheat, spring wheat and hay are more likely to be chosen as reg

295 ially expressed genes between the winter and spring wheat genetic backgrounds showed a striking patte

296 Many of the irrigated spring wheat regions in the world are also regions with

297 Higher content of total tocols was found in spring wheat varieties compared with winter varieties.

298 e coumarin absorbances in summer, winter and spring whereas mixtures without ethanol show no signific

299 t using immobilized probe 1 and probe 2 with SPR which showed the applicability of this methodology a

300 or change, due to surface plasmon resonance (SPR), which occurs in about 30min of total assay time wh

301 low in summer, but uncertainty is larger for spring with only half of the simulations suggesting a we