ライフサイエンスコーパス: incubation time

1 the protocol is 2-4 h (including 45 min-3 h incubation time).

2 re sophisticated sample preparation and long incubation time.

3 (AEK) in 37 degrees C mixtures regardless of incubation time.

4 ld be substituted by an acquisition at fixed incubation time.

5 ciation of targeted liposomes increases with incubation time.

6 cing the quantity of ionic gold and required incubation time.

7 is rate-limiting step requires up to 12 h of incubation time.

8 asurement with 1 muL sample volume and 5 min incubation time.

9 ere recorded for cell media as a function of incubation time.

10 persistence and contour length depend on the incubation time.

11 te in the perinuclear region with increasing incubation time.

12 cubation step with a 6-fold reduction in the incubation time.

13 sylation protocols usually require a lengthy incubation time.

14 stronger heterocyclic forms with increasing incubation time.

15 Lack of Sho protein did not affect prion incubation time.

16 s with expression levels that correlate with incubation time.

17 vous system, starting already halfway in the incubation time.

18 ) prion inoculation, shows a 4% reduction in incubation time.

19 by modulating the initial concentration and incubation time.

20 mplify the detection method and decrease the incubation time.

21 sis, which correlated with the length of the incubation time.

22 urological dysfunction marked the end of the incubation time.

23 ndent on the concentration of 2-ClHA and the incubation time.

24 nd aptamer concentration, flow velocity, and incubation time.

25 ght of cleavage product formed after a fixed incubation time.

26 amount of cell lysate protein after a fixed incubation time.

27 -h incubation time (37 nM) than with a 5-min incubation time.

28 logical phenotype as reflected by a specific incubation time.

29 estion of BAEE at 20 degrees C after 16 h of incubation time.

30 ociated with soil depth, sampling method and incubation time.

31 s and including conjugation, sonication, and incubation time.

32 pH 7.0, temperature 25 degrees C and 6min of incubation time.

33 volatile compounds, regardless of dosage or incubation time.

34 similar to that of a conventional 1-hour ALA incubation time.

35 spholipid among HDL species as a function of incubation time.

36 ng while significantly reducing the required incubation time.

37 proof-of-concept study, but requiring longer incubation time.

38 ilayer cholesterol content, temperature, and incubation time.

39 changing the adenosine concentration and the incubation time.

40 be determined by the applied power and cell incubation time.

41 in trapping agent should be given the proper incubation time.

42 MMP-9 was not observed even after prolonged incubation times.

43 ansmission, changing host susceptibility and incubation times.

44 ncentration range of the analyte at specific incubation times.

45 ease in wild-type mice with relatively short incubation times.

46 ds generated less stable strains and shorter incubation times.

47 ss the effect the GSI plus Qa combination on incubation times.

48 namic assay were expected due to the shorter incubation times.

49 ssay formats, including those requiring long incubation times.

50 end toward increased positivity at prolonged incubation times.

51 low (1 muM) concentrations and short (5 min) incubation times.

52 -to-enzyme ratio (S/E ratio, 20 and 50), and incubation time (0.5, 1, 2 and 5h) were evaluated based

53 t gluten samples incubation temperatures and incubation times (0, 90 or 135 min at 30 degrees C and a

54 t and trout liver S9 fractions for different incubation times (10, 30, and 60 min) at 2 concentration

55 red wines), temperature (85 degrees C), pre-incubation time (15min) were optimized for identificatio

56 plain Mueller-Hinton [MH] agar), (ii) three incubation times (16 to 24, 48, and 72 h), and (iii) sev

57 ase dose - 4.5% w/v, inoculum age - 48 h and incubation time - 24 h) reached 325 g/L (55% yield) with

58 : temperature=50 degrees C, S/E ratio=50 and incubation time=2h, exhibited the highest DPPH radical s

59 at a signal-to-noise ratio of 3), and short incubation time (30min).

60 ging and was 3.2-fold more potent with a 1-h incubation time (37 nM) than with a 5-min incubation tim

61 -FeO(OH) (goethite) nanoparticles at various incubation times (4 or 48 h).

62 ecificity for AFP detection, extremely short incubation time (5 min), good stability and acceptable r

63 Thermal treatments at different incubation times (5, 10 and 15 min) and different pH (4,

64 molar ratio 1/15, enzyme load 30% (w/w) and incubation time 6 days.

65 At longer incubation times (6 hours), gene array analysis revealed

66 c tool featuring better sensitivity, shorter incubation time, accessibility, and low sample and reage

67 inute or 20-minute aminolevulinic acid (ALA) incubation times, after pretreatment with a microneedle

68 Significant reduction of incubation time along with considerable lower detection

69 erimental parameters like OTS concentration, incubation time and addition of a silver reduction step

70 e the effective parameters (pH, temperature, incubation time and concentration of aptamers) are inter

71 al controls for establishing the appropriate incubation time and concentration regime were not docume

72 ioxidant capacity by up to 80%, reducing the incubation time and enzyme doses in respect to previous

73 Because of the long incubation time and highly complex disease pathogenesis,

74 s, with most of the tumors showing shortened incubation time and malignant progression.

75 This synchronization method decreases incubation time and media consumption and improves synch

76 cereus spores 14579 evaluating the effect of incubation time and MgCl(2) concentration.

77 hanging the RPA reaction conditions, such as incubation time and primer concentration, has little eff

78 dence of the uroporphyrinogen I formation on incubation time and protein amount.

79 ne moiety of DNPH decreases as a function of incubation time and protein concentration.

80 le to inhibit candidal growth following 18 h incubation time and reduced the minimal inhibitory conce

81 the superiority of the LC system concerning incubation time and sensitivity.

82 oculum size of 1 to 3 x 10(3) CFU/ml, and an incubation time and temperature of 96 h at 35 degrees C.

83 pressing the MR is examined as a function of incubation time and temperature, nanocarrier size, dose,

84 parameters, such as concentration of enzyme, incubation time and temperature, was optimised.

85 Temperature, incubation time and the concentration of acetic acid wer

86 results demonstrate the importance of assay incubation time and the degree of receptor reserve in ap

87 impact on the response, i.e. the anti-tetani incubation time and the dilution factor of the labeled a

88 n of the resulting prions produced prolonged incubation times and altered PrP(Sc) deposition patterns

89 pore water, which increased with longer soil incubation times and decreasing soil pH.

90 ng levels of performance (i.e., reduction of incubation times and detection limits) demanded in the m

91 In conventional immunoassays, long incubation times and excess amounts of the recognition a

92 eater effects generally observed with longer incubation times and higher concentrations.

93 al that lack of ADAM10 significantly reduces incubation times and increases PrP(Sc) formation.

94 ferromicrofluidics in significantly reducing incubation times and increasing diagnostic sensitivity i

95 as bovine serum albumin (BSA) concentration, incubation times and labeled antibody dilution, were opt

96 We show that MoSP1 gradually adopted shorter incubation times and lower conformational stabilities.

97 However, prolonged incubation times and pain associated with treatment are

98 agate in vivo and cause disease with defined incubation times and patterns of neuropathology.

99 e biomarker recognition, which leads to long incubation times and significant reagent demands.

100 tions of the virus-Fab complex for different incubation times and structural analysis provide a model

101 nal process parameter maps link the nanotube incubation times and the relative differences between th

102 lectric field frequency, cell concentration, incubation times and the type of blocking agent to achie

103 and 2 phosphorylation assays that have short incubation times and therefore are prone to hemi-equilib

104 bled microwell plates in such a way that the incubation times and volumes can be reduced substantiall

105 ubble-bursting experiments (with contrasting incubation times and, likely, physiological microalgal s

106 , incubation pH, DNA-AuNP concentration, and incubation time) and the separation scheme (sample loadi

107 1) the analyte concentration, (2) the sample incubation time, and (3) the sample volume, resulting in

108 between tissue excision and staining, agent incubation time, and agent dose, and translated our stra

109 ssay exhibits good tolerance to temperature, incubation time, and dimethyl sulfoxide concentration.

110 e influence of three continuous factors (pH, incubation time, and enzyme concentrations), in the rang

111 ts showed that surfactant concentration, pH, incubation time, and ionic strength exert significant ef

112 ion and separation solutions, extraction and incubation time, and solvent volume were also investigat

113 n could be influenced by drug concentration, incubation time, and surface coating, as well as the typ

114 In addition, the large sample volume, long incubation times, and single-plex configuration have bro

115 mination of washing steps, the shortening of incubation times, and the use of lower XTT concentration

116 Minimal brain spongiosis and long incubation times are observed for the BASE strain-infect

117 , require manual manipulations, have lengthy incubation times, are limited to one collection, and lac

118 physiologically relevant levels (pg/mL) with incubation times as short as 2.5 min.

119 ntration, amounts of bacterial inoculum, and incubation times as short as 6 to 8 h.

120 (Sc) caused a disease with indistinguishable incubation times as well as neuropathological and bioche

121 oncentrations of detergents or lipoproteins, incubation time, as well as the order of mixing reaction

122 not prevent infection but instead shortened incubation time, as would be expected for a viral recept

123 By means of an applicable incubation time between cell cycle period and proper sta

124 e agents were clearly different from kuru in incubation time, brain neuropathology, and lymphoreticul

125 that reduced the detection limit and sample incubation time by up to 5-fold and 2-fold, respectively

126 entrations, CMT-ELISA offered a reduction in incubation times by 90-95%, facilitating a very fast tur

127 We show that these incubation times can be accounted for by purely thermal

128 Although incubation times can be changed by altering the PrP expr

129 Depending on cold pre-incubation time, caseinomacropeptides accumulated well b

130 that the increase in temperature and gluten incubation time caused the increase in the amount of fre

131 However, at short incubation times cell death seems to be mainly caspase d

132 employed to optimize parameters such as pH, incubation time, cloud point temperature and surfactant

133 Variations in media, temperature, incubation time, CO2 level, and inoculum concentration w

134 hin 3h, which is at least 3-fold decrease in incubation time compared to conventional microarrays.

135 The parameters that were optimized included incubation time, concentration of RapiGest SF, enzyme-to

136 (NADC 13-7) in order to assess the stability/incubation time correlation in a natural host system.

137 , and fit the model to in vivo data on prion incubation times corresponding to different levels of Pr

138 amic focusing to achieve highly reproducible incubation times (CV = 3.6%).

139 To test this hypothesis, we combined incubation time data from five different inbred lines of

140 inhibition was competitive; however, longer incubation times demonstrated the inhibition to be irrev

141 ncreatic cancer cells in a concentration and incubation time-dependent manner.

142 wever, expedited exposure of a 10-minute ALA incubation time did not reach significantly different AK

143 synthetic prions, two isolates emerged with incubation times differing by nearly 100 days.

144 cholesterol incorporation, temperature, and incubation time directly alter the conformer preferences

145 Creamed emulsion assay incubation time dispersion was 1.7%, 3-fold less than ot

146 profiles that may result from the prolonged incubation times (e.g., overnight enzymatic treatment fo

147 zation conditions including pH, temperature, incubation time, enzyme concentration, and mediator addi

148 Under the optimized conditions (incubation time equal to 3 h and absence of MgCl(2)), B.

149 odilution method that requires a 16- to 20-h incubation time for B. anthracis Advances in high-resolu

150 Our results show that the incubation time for carbon transport through the oxide s

151 ed in decreased disassembly times, decreased incubation time for onset of disassembly from minutes to

152 2 days for sample processing, including the incubation time for proteolysis.

153 oximately 24-26 h to complete, including the incubation time for proteolytic digestion.

154 chimeric transgene from I to M prolonged the incubation time for sCJD(MM1) prions by more than 100 da

155 The overall incubation time for the assay was reduced by approximate

156 IND24 doubled the incubation times for mice infected with CWD prions but h

157 A reduction of incubation time from 10min to 2min increased the method

158 Similarly, high temperature for the same incubation time gave longer segments.

159 Longer incubation times gave longer segments at the same temper

160 rion isolates enciphering shorter and longer incubation times, [Gdn.HCl](1/2) values of 2.9 and 3.7 M

161 ature ( degrees C), enzyme concentration and incubation time (h) were optimized by central composite

162 At longer incubation times, however, the Pt:As ratio in DNA sample

163 Longer incubation times illuminate downstream events that drive

164 gradient ultracentrifugations, and a longer incubation time in animal bioassays.

165 id progression of disease onset, whereas the incubation time in bats inoculated s.c. is significantly

166 the effect of probe concentration and probe incubation time in the platelets prior to measurement of

167 s were universally up-regulated at all three incubation times in response to desiccation, an addition

168 Compared to disease incubation times in wild-type homozygous ARQ/ARQ (where

169 Generally, increasing incubation time increased the contents of various phenol

170 he polymerization process, while a prolonged incubation time increases the amount of Py accumulated o

171 The effect of incubation time, incubation temperature, and enzyme conc

172 However, the prolonged incubation times involved lead to turnaround times of ty

173 However, when the incubation time is 3h, the limit of detection (LOD) for

174 optimal temperature of 37 degrees C, if the incubation time is extended from 10 min to 3 hr.

175 ing a fast-acting scrapie inoculum for which incubation time is highly dependent on the amino acid at

176 et of solubilization and little dependent on incubation time; it is accompanied by fast lipid scrambl

177 in low-resource settings is limited by long incubation time, large volumes of precious reagents, and

178 nt tris(2-carboxyethyl)phosphine (TCEP), pH, incubation time, linearity of labeling, and saturating d

179 , dimers and other low MW oligomers at early incubation times (< 1h) are consistent with a hairpin st

180 lengths of over 40 nm are observed at short incubation times (< or = 3h); their lateral dimensions o

181 In some cases it is possible that incubation time may be directly correlated to the level

182 s culture and demonstrates that solid medium incubation times may be reduced to 6 weeks without signi

183 nditions of the spin trapping agent (such as incubation time) may lead to misinterpretation of the re

184 The incubation times, neuropathological lesion profiles, and

185 nd that prions causing CWD in Norway induced incubation times, neuropathology, regional deposition of

186 M upon intracellular calcium imaging with an incubation time of 1 h, compared with an EC50 value of 2

187 e presence of saturating 4-OHT over an assay incubation time of 1-6 h, indicating an excellent assay.

188 of 37 degrees C, agitation at 100 rpm and an incubation time of 10h with variable pH (5-7) and salt c

189 trode detection limit was 28cellsml(-1) with incubation time of 10min.

190 ng low detection limit of 10 cellsmL(-1) and incubation time of 10min.

191 /40microL (i.e., 19-6250ng/mL), both with an incubation time of 10min.

192 had a detection limit of 2.6pgmL(-1) with an incubation time of 15min.

193 3 exhibited highly significant reductions in incubation time of 16, 15, and 7% following infection wi

194 rough organ transplantation with an observed incubation time of 17-24 days.

195 vourzyme(R), temperature 50 degrees C and an incubation time of 1h.

196 (enzyme-to-substrate ratio of 2.5:1), and an incubation time of 2 h.

197 uAD's response time is of 50 s, including an incubation time of 20 s.

198 l(-1), detection limit of 20cellsml(-1) with incubation time of 20min for FA based electrode, and for

199 incubation temperature of 45 degrees C, and incubation time of 30 min.

200 After an incubation time of 30 s, bead fluorescence is measured u

201 sensor showed a good linearity range with an incubation time of 4min for Malathion and Acephate, resp

202 ing the developed ANN-GA were as follows: an incubation time of 64 min, incubation temperature of 32

203 2 mg COD/L of CH(3)OH was produced within an incubation time of 7 h, which is approximately ten times

204 s tightly and positively correlated with the incubation time of disease upon passage into mice.

205 In addition, the incubation time of DNA with cells and the presence of di

206 er a period of 348 s, was found to vary with incubation time of each biofilm in correlation with the

207 imit of detection of 3 x 10(2) cfu/mL and an incubation time of only 1 h.

208 he direct relationship between stability and incubation time of prion strains suggests that labile pr

209 odifications is directly proportional to the incubation time of protein samples in the reduction/alky

210 meters (e.g., concentration of Ru(bpy)3(2+), incubation time of TNF-alpha, etc.) were optimized.

211 Incubation times of 140 days and a rate of prion infecti

212 t and second passage, the FVB mice exhibited incubation times of 154 +/- 4 and 130 +/- 3 days, respec

213 ffusion testing were (i) plain MH agar; (ii) incubation times of 16 to 24 h (zygomycetes), 24 h (Aspe

214 ies of silver spots to the concentration and incubation times of antigens and gold nanoparticles.

215 e early studies, resulting in estimated mean incubation times of approximately 5 days.

216 These results suggest that incubation times of enzymes and flavonoids shall be eval

217 bution of the DNA-HU complex after different incubation times of HU with linear DNA.

218 mes and the relative differences between the incubation times of SWCNTs of different sizes/chiralitie

219 , but also to better selectivity between the incubation times of SWCNTs with different sizes and chir

220 technique or immunoassays depends highly on incubation times of the recognition elements or signalin

221 ctivities in a wide pH range (4-11) and with incubation times of up to 24 h in droplet-based microflu

222 ansmission characteristics, including longer incubation times, of the inoculated vCJD strain; the sec

223 ined effects of pH, enzyme concentration and incubation time on biosensor response were optimized usi

224 The effects of sugar concentration and incubation time on the AGE profile are also reported for

225 The observed dependence of the incubation time on the degree of undercooling is consist

226 cts of different enzymes, their dosages, and incubation times on juice yield and chemical composition

227 get DNA concentrations with relatively short incubation times, only a small percentage of the capture

228 be mostly compensated for by increasing the incubation time or concentration of ISW2.

229 sphorylation defect was not reversed by long incubation times or high TRH concentrations.

230 Current model systems require very long incubation times or severe immune suppression, and tumor

231 hers confer protection, dramatically altered incubation times, or changes in the clinical phenotype.

232 he interactive effect of enzymatic units and incubation time (p-value <0.015), while CER was found to

233 sease, including vCJD (p=5.6 x 10(-5)), kuru incubation time (p=0.017), and resistance to kuru (p=2.5

234 y and clinical signs at significantly longer incubation times (P<0.0001 for both comparisons).

235 The effects of the incubation time, pH and metal ions concentrations on the

236 ) structural states enciphers a multitude of incubation-time phenotypes.

237 on, we report here the ability to modify the incubation time predictably in mice by modulating the pr

238 res to interfere with replication of a short-incubation time prion strain was investigated.

239 ed the prospect of reducing the carrot broth incubation time prior to PCR performance.

240 It was found that a long incubation time produced sensitive results, but was not

241 onsidered to optimize the conditions include incubation time, protein concentration, limit of detecti

242 array of fibrinogen dots after a predefined incubation time quantitatively assays platelet adhesion

243 Average catalase activity for the same incubation times ranging from 1 to 12 h was found to be

244 less of the methylation reaction conditions (incubation time, reaction volume, and substrate concentr

245 increased probe concentrations and decreased incubation time removed the need for masking DNA, furthe

246 , specialized wash protocols and the lengthy incubation times required by other published recombineer

247 08/Val-189) is associated with short or long incubation times, respectively, following infection with

248 d genes were common to the 4/24- and 24/72-h incubation times, respectively.

249 oke/min shaking speed at 40 degrees C for 1h incubation time resulted in highest oil recovery of appr

250 AFM images obtained as a function of incubation time reveal a sequence of assembly from monom

251 mber of experimental variables: temperature, incubation time, salt concentration, pH, lipid compositi

252 D); on second passage in Tg(BoPrP) mice, the incubation times shortened by 30 to 40 days.

253 uld be small, while the anti-tetani antibody incubation time should be long.

254 microneedle pretreatment at a 20-minute ALA incubation time significantly improved AK clearance with

255 d the impact of control parameters including incubation time, stability of the signal, temperature, a

256 n a disease that closely mimics human HPS in incubation time, symptoms of respiratory distress, and d

257 ternalization was monitored as a function of incubation time, temperature, nanoparticle diameter, and

258 e found that species with relatively shorter incubation times tended to show greater phenotypic varia

259 with 10-fold less enzyme and 15-fold shorter incubation times than required when using T4 DNA ligase.

260 ithin the gels enables significantly shorter incubation times than standard surface DNA microarrays.

261 es result in its metallization only after an incubation time that ranges from approximately 150 ps to

262 PrP transgenes produced profound changes in incubation times that allowed us to distinguish prions c

263 ssessing bacterial populations requires long incubation times that are not compatible with a tight co

264 Depending on incubation time, the preparation showed pH-optimum at 2.

265 zed TNA synthesis at different temperatures, incubation times, tNTP ratios and primer/template combin

266 by drastically decreasing the library-ligand incubation time to 30 s.

267 (18)F-FDG, with variation in temperature and incubation time to determine optimal conditions.

268 The newly emerged strain has the shortest incubation time to disease and is characterized by coloc

269 considered kinetic studies to establish the incubation time to perform the assay.

270 ormational stability of synthetic prions and incubation time to prion disease.

271 varied atmospheric conditions, and prolonged incubation times to demonstrate that many of the organis

272 teins, varying pH, enzyme concentrations and incubation times to simulate infant and young child gast

273 ce polymers are unable, even after prolonged incubation times, to adopt stable helical structures by

274 inued up to approximately 2 h, comparable to incubation times used with HIV-1 PIC.

275 one in standard culture media with prolonged incubation times using gas-exchanging culture containers

276 ined at different pH values and at different incubation times, using beef and chicken samples.

277 4 degrees C as at 37 degrees C, provided the incubation time was also extended to 3 hr.

278 lower reagent volumes but also the required incubation time was considerably reduced and a notable i

279 The incubation time was determined by the time needed for ce

280 ovine fetuin as a standard glycoprotein, the incubation time was determined for each major step of gl

281 higher toxin concentrations, whereas a short incubation time was less sensitive so that lower toxin c

282 ication (OPI) algorithm with an increased T4 incubation time, we demonstrated cell cycle arrest and a

283 receptor concentration, temperature, pH, and incubation time were optimized to obtain the high sensit

284 ined with the dynamic assay for 25- and 47-s incubation times were 290 and 250 microM Triton X-100, r

285 Different inoculation methods and incubation times were evaluated to determine the optimal

286 oassay when the quantity of the reagents and incubation times were kept constant, which is also an in

287 Longer incubation times were observed for the blood donor splee

288 When the incubation times were plotted as a function of the [Gdn.

289 Higher concentrations of Abetaf and longer incubation times were required to produce widespread neu

290 ionic strength, incubation temperature, and incubation time, were investigated and optimized by orth

291 conditions, such as reagent consumption and incubation time, were optimized in the microchip platfor

292 lower agonist concentrations and at shorter incubation times when G proteins were not limiting, the

293 maximum inhibition of HSA and PPA with short incubation time whereas maximum inhibition of HSA and PP

294 ble prion strains that exhibited the longest incubation times, whereas more labile amyloids generated

295 lifetimes of the probe at longer Antimycin A incubation times which lay outside of the O2 concentrati

296 eps, significantly reducing antigen-antibody incubation times, while maintaining antibody specificity

297 to magnetism, sample preparation and proper incubation time with spin trapping agents.

298 ance, such as the amount of MC1R-Abs loaded, incubation time with the target melanoma cells, the pres

299 BKV LAMP was performed using various incubation times with a variety of specimens, including

300 alysis was complete within 20 min (including incubation time) with RNA detection limits of 0.125 nM a