ライフサイエンスコーパス: lane

1 each mRNA sample only once (i.e., using one lane).

2 samples were multiplexed at four genomes per lane.

3 d, color-coded amplification product per gel lane.

4 load many PCR products in a single capillary/lane.

5 lusion of an internal size standard in every lane.

6 hich contained internal size markers in each lane.

7 all the data across the entire width of the lane.

8 exogenous autoinducer at one terminus of the lane.

9 d time as the autoinducer diffused along the lane.

10 1, CJ360, CJ394, CJ970, and OD4, in a single lane.

11 , is analyzed in a gel with suitable control lanes.

12 icrofabricated chip with parallel separation lanes.

13 ility between the same fragment on different lanes.

14 rs, with different reagents deposited in the lanes.

15 , CS-B, and CS-E and avoided CS-C containing lanes.

16 lets with a metal sliding device along these lanes.

17 e varying depending on proximity to shipping lanes.

18 or extracellular signaling we made cell-free lanes 10-300 microns wide in confluent cultures by delet

19 t of the expressed transcripts (80-120 bands/lane), 26 different 5' primers were used in conjunction

20 A stroll down the memory lane 70 years back, this might have sounded utopian.

21 e to a vehicle that unexpectedly blocked the lane ahead.

22 In a stripe assay, however, where M1-4 lanes alternate with polylysine-(Plys)-only lanes, RGC a

23 ermination of the model parameters; and data lane analysis, a procedure for detecting restriction fra

24 form consistent with a linear model; marker lane analysis, for determination of the model parameters

25 h fragment mobility), an artifact of lane-to-lane and gel-to-gel differences, was controlled with an

26 The software uses models of expected lane and interlane spacing and lateral lane behavior to

27 ilization drove focused proteins off the IEF lane and into a region for protein gel electrophoresis.

28 We embedded a QS strain in a narrow agar lane and introduced exogenous autoinducer at one terminu

29 ) and using only approximately 10 sequencing lanes and approximately 10 distinct barcodes per lane, o

30 devoted to each molecule reduces sequencing lanes and cost, with little loss in detection power.

31 some of the solid pharmaceutical across the lanes and dips the edge of the paper into water.

32 Lanes and lane boundaries are tracked by analyzing a fir

33 multiplex sequencing of up to 96 samples per lane, and is strand specific.

34 Barriers, growth lanes, and pinning structures comprised of crosslinked p

35 asilinear time processing of entire Illumina lanes ( approximately 10(7) sequences) on a desktop comp

36 rived from a single Illumina Genome Analyzer lane, approximately 94% (approximately 50,500) target si

37 Initially lanes are located in a region of the gel image selected

38 The 384 capillary lanes, arrayed radially about the center of a 200-mm-dia

39 ior change in psychotherapy is needed, which Lane at al. advance.

40 To define the IEF axis along a "lane" at the top of the chamber, we used free solution c

41 AO) and disc space narrowing (DSN) using the Lane atlas at each lumbar disc space (L1-5).

42 Software to track sample lanes automatically in four-color, fluorescence-based, e

43 ll subsequent steps of analysis on a lane by lane basis and allows for uniform comparison of the gene

44 ected lane and interlane spacing and lateral lane behavior to maintain accurate tracking on imperfect

45 Lanes and lane boundaries are tracked by analyzing a first differe

46 ls for all subsequent steps of analysis on a lane by lane basis and allows for uniform comparison of

47 As water climbs up the lanes by capillary action, it triggers a library of diff

48 ntal conditions are resolved in two separate lanes by gel electrophoresis.

49 es background banding patterns to facilitate lane calling and size calibration.

50 A microfabricated 384-lane capillary array electrophoresis device is developed

51 ays were combined and loaded on a single gel lane/capillary to substantially improve throughput.

52 nduced shocks in the general case of nonzero lane changing rates.

53 Lane-Claypon described, discussed, and analyzed her data

54 In 1912, Janet Elizabeth Lane-Claypon, a British medical scientist 35 years of ag

55 andard, we observed spot-to-spot and lane-to-lane coefficients of variation of less than 10 and 20%,

56 fic landmarks and traffic signs along a four-lane commercial strip during an experimental drive in an

57 lpha 233 presents a narrow, unpolarized dark lane consistent with an optically thick circumstellar di

58 nt of neurites was observed using underlying lanes containing CS-A, CS-B, and CS-E chains.

59 ameters determined empirically from "marker" lanes containing molecular size standards.

60 ncing technologies, both in the form of high lane-density gels and automated capillary systems, will

61 ensory modalities as the driver detected the lane-departure in a simulated driving task would promote

62 translated to significantly larger range of lane departures only in the case of sensorimotor and mix

63 motional stressors, often a smaller range of lane departures was observed, indicating safer driving w

64 regions of confluent astrocytes separated by lanes devoid of cells were easily located.

65 bes appropriate for base-calling in a single-lane DNA sequencing format.

66 es a weakly and asymmetrically coupled three-lane driven diffusive system.

67 In this issue of Developmental Cell, Lane et al. (2015) describe a simplified, inexpensive te

68 in recent issues of Molecular Pharmacology, Lane et al. and Galandrin and Bouvier, provide new mecha

69 Lane et al. are right: Troublesome memories can be thera

70 Lane et al. argue that any psychotherapeutic interventio

71 Lane et al. emphasize the role of emotional arousal as a

72 Lane et al. imply hypotheses that are questionable: that

73 and the recognition of its critical role by Lane et al. is a welcome development.

74 Lane et al. propose a heuristic model in which distinct,

75 Lane et al. propose an integrative model for the reconso

76 Lane et al. propose that memory reconsolidation through

77 The Lane et al. study clearly demonstrates G protein-specifi

78 I point to several ways in which Lane et al. successfully use multilevel explanations to

79 We share the idea of Lane et al. that successful psychotherapy exerts its eff

80 ation integrating new emotional experiences, Lane et al. usefully shift the focus away from establish

81 Lane et al. view the process of memory reconsolidation a

82 Lane et al.'s proposal that psychotherapeutic change com

83 lled "psychopathology" are very diverse, but Lane et al.'s single-process explanation does little to

84 Like Lane et al., we believe that change in psychotherapy com

85 ticipants had a significantly higher rate of lane excursions, average Johns Drowsiness Scale, blink d

86 Driving performance measures included lane excursions, near-crash events, and drives terminate

87 0 kDa bands (pentameric PLB) within the same lanes exhibited low anisotropy, suggesting intrapentamer

88 orrelation is also used to locate and define lane features.

89 can enter a cavity and use it as an express lane for a fast margination toward the wall.

90 el for PAGE and blotting to an "open" PA gel lane for immunoprobing and readout.

91 ts of $0.10-$0.20 per cell and includes five lanes for simultaneous experiments.

92 e nonspecific shift band in negative control lanes from which protein extracts were omitted.

93 The reactions in each lane generate colors to form a "color bar code" which ca

94 e prepared off-chip and analyzed on a single-lane glass microchip fabricated by standard methods.

95 cally changing density profile in the middle lane has been observed.

96 ts oxidation along the oxidative/oxygenative lanes have been studied from a mechanistic point of view

97 e particle ATOFMS spectra collected on a six lane heavily trafficked road in central London (Marylebo

98 or imaging of analyte bands in a development lane (i.e., multiple lane scans with close spacing).

99 ols implemented in SAFA have five steps: (i) lane identification, (ii) gel rectification, (iii) band

100 a during surface scans along the development lane in the direction of increasing Rf value.

101 ves crossed narrow (< 120 microns) cell-free lanes in 15 of 36 cases, but failed to cross lanes wider

102 s resolution of multiple samples in parallel lanes in a single run.

103 Some lanes in the immunoblots were used to represent differen

104 of the Western blot with the silver-stained lanes indicated the presence of a single lightly stained

105 Lane intensity on the autoradiograph was linearly relate

106 The newly discovered Drop 45 Drive Lane is the most complex hunting structure found to date

107 Lane keeping (steering instability and crossing the cent

108 siness and other driving measures, including lane keeping and response to a vehicle that unexpectedly

109 ramps, parking in the correct space, seeing lane markings, and reading signs.

110 egradations including significant horizontal lane motion (curving) and image artifacts, and is now in

111 l slices were excised from each of three gel lanes (n = 99), digested with trypsin, and subjected to

112 electroeluates from six gel electrophoretic lanes needed to be pooled; (iii) excessive protein loads

113 ical variation, library preparation and chip/lane noise), allowing a separation and comparison of the

114 ion submicrometer-sized colonies in a single lane of a next-generation sequencing flowchip.

115 od that is performed by electrophoresing one lane of a Sanger dideoxy termination reaction through a

116 up to a hundred individual cells on a single lane of an Illumina HiSeq instrument.

117 With a single library and one lane of Illumina HiSeq sequencing, we increased the scaf

118 One lane of Illumina sequence was sufficient to call high-co

119 A single lane of Illumina sequences allowed accurate and quantita

120 The information in a single lane of Illumina sequencing data appears comparable to t

121 A single lane of Illumina sequencing permitted methylation states

122 stein-Barr virus (EBV) genomes from a single lane of next-generation sequencing (NGS) reads.

123 For collagen arrays where only the center lane of spots (in the direction of flow) contained TF, a

124 of a single freestanding polyacrylamide gel lane of varying cross-sectional width.

125 e run on multiple lanes of a single gel, one lane of which was transferred to PVDF membrane and probe

126 l mobilities are electrophoresed on separate lanes of a denaturing gel to reveal how each strand gap

127 crude membrane fraction were run on multiple lanes of a single gel, one lane of which was transferred

128 a 300-micrometer gap to the adjacent TF-free lanes of collagen spots, in agreement with numerical sim

129 ghways' that consist of alternating parallel lanes of conjugated polymer and CdSe.

130 CS variant between the microcontact printed lanes of CS-C stripes, which are avoided by neurons.

131 haracterized size standard in at least three lanes of each gel.

132 etry (MAMS) technology and contains parallel lanes of hydrophilic reservoirs.

133 On the basis of two lanes of Illumina sequencing, we inferred phylogenetic r

134 al crest cells in vitro avoided migrating on lanes of immobilized ephrin-B1; the addition of soluble

135 Two gels containing 38 lanes of SmaI-digested Enterococcus faecalis OG1RF DNA w

136 jected directly into the parallel separation lanes of the chip via a capillary at predetermined time

137 n (LAMP) reagents predeposited into distinct lanes of the microfluidic chip, which when exposed to ta

138 rs per second from the narrow bright network lanes of this interface region.

139 A single "lane" of paired-end sequences (2 x 76 bp) provides a goo

140 right sides and approached the participant's lane on a collision trajectory that, therefore, caused t

141 -backcross individuals genotyped in a single lane on an Illumina Genome Analyzer.

142 nscript in the heart and skeletal muscle RNA lanes on a multitissue Northern blot.

143 f automated scanning of multiple development lanes on a reversed-phase C8 TLC plate and by imaging in

144 Computer-controlled scanning of development lanes on the plate was illustrated by using multiple ion

145 e spots), scanning of a complete development lane (one or multiple lanes), or imaging of analyte band

146 s and approximately 10 distinct barcodes per lane, one recovers the identity of 4 rare allele carrier

147 tion and analyzed simultaneously in a single lane or capillary.

148 single reaction that is analyzed in a single lane or capillary.

149 ace scanning along the length of development lanes or at fixed Rf value across the plates versus the

150 a complete development lane (one or multiple lanes), or imaging of analyte bands in a development lan

151 DNA sequencing data from 95 successful lanes out of 96 lanes run in parallel were batch-process

152 allele frequencies can be estimated from one lane per locus.

153 lower numbers, requires a single PCR and gel lane per sample.

154 s one user to run up to several-thousand gel lanes per day for the direct assay of single-base variat

155 Lane position and steering stability were evaluated for

156 Varying the lane position of standards on a gel and using gel plugs

157 yzed to assess the impact of (i) varying the lane position of the standards, (ii) using gel plugs mad

158 The drivers with right HH held a lane position significantly (P = 0.001) to the left of N

159 The drivers with left HH had a lane position similar to that of the NV drivers on strai

160 D demonstrated more variability in speed and lane position than control subjects.

161 with homonymous hemianopia (HH) would take a lane position that increased the safety margin on their

162 t the hypothesis that drivers with HH take a lane position that increases the safety margin on their

163 argin on their blind side; however, absolute lane position varies as the steering maneuver and locati

164 denced by increased variability in speed and lane position.

165 It can be used for gel visualization, lane retracking, and as a front end to the Washington Un

166 lanes alternate with polylysine-(Plys)-only lanes, RGC axons from goldfish, zebrafish, and chick ret

167 n residential streets, intermediate (1- or 2-lane) roads, highways, rural roads with curves and eleva

168 cing data from 95 successful lanes out of 96 lanes run in parallel were batch-processed with basefind

169 the influence of probe-to-surface distance, lane scan spacing, and surface scan speed on signal qual

170 The ability to spot sample, lane scan, and chemically image in an automated and cont

171 changing topography of the surface during a lane scan.

172 The system was used for lane scanning and chemical imaging of the cationic dye c

173 Both lane scanning and spot sampling mass spectral imaging mo

174 With use of a lane scanning mode with approximately 6 mum x approximat

175 bands in a development lane (i.e., multiple lane scans with close spacing).

176 These paper devices contain 12 lanes, separated by hydrophobic barriers, with different

177 they comigrated, indicating that, in single-lane sequencing applications, when utilizing these dyes,

178 e lifetime base calling to a single-dye/four-lane sequencing strategy indicated similar results in te

179 abeling (IRD700 and Cy5.5 labeling dyes)/two-lane sequencing strategy, we successfully read 670 bases

180 Using an in-lane size standard labeled with a fifth dye, fragments a

181 f the gel image selected for good horizontal lane spacing and signal strength.

182 robe-to-paper surface distance of 5 mum, and lane spacing of 10 mum were used for imaging.

183 differences, was controlled with an internal lane standard, resulting in accurate and precise DNA siz

184 point and with double internal calibration (lane standards and gene standards).

185 ifferent durations were measured along a two-lane street of one-way traffic without a traffic signal.

186 d rat M1-4 but freely crossed zebrafish M1-4 lanes-suggesting that zebrafish M1-4 is growth permissiv

187 anding polyacrylamide gel (fsPAG) separation lanes supports 384 concurrent EMSAs in 30 s using a sing

188 ring with fragment mobility), an artifact of lane-to-lane and gel-to-gel differences, was controlled

189 ernal standard, we observed spot-to-spot and lane-to-lane coefficients of variation of less than 10 a

190 ss and performance lapses, as well as poorer lane tracking, were associated with shorter sleep durati

191 The rate of lane-tracking errors is very low, approximately 0.5%.

192 f papG could be resolved by size in the same lane using agarose gel electrophoresis after simultaneou

193 increase when the total protein load per gel lane was reduced from 30 to 1 microgram.

194 The probability of crossing narrow lanes was not correlated with the distance from the stim

195 Calculated velocity across the acellular lanes was not significantly different from velocity thro

196 , another car suddenly merging into driver's lane) was introduced.

197 Development lanes were scanned by moving the TLC plate under compute

198 The remaining lanes were silver-stained.

199 and a corresponding region from an adjacent lane where the product is less prominent or not visible.

200 d with a CCD camera as they separated in the lanes, which were filled with linear polyacrylamide.

201 lanes in 15 of 36 cases, but failed to cross lanes wider than 120 microns in eight of eight cases.

202 the seven genomes were sequenced in a single lane with average coverage ranging from 224 to 1345.

203 Detection of all lanes with high temporal resolution was achieved by usin