ライフサイエンスコーパス: bait

1 on to glucose (a phagostimulant component of baits).

2 s it possible to immobilize new biotinylated bait.

3 bridge between the chip and the biotinylated bait.

4 one-hybrid system and the OsNHX1 promoter as bait.

5 ng the cytosolic domains of ETR1 and ETR2 as bait.

6 nd consumed a large proportion (>50%) of the bait.

7 t two-hybrid assay using NKCC2 C terminus as bait.

8 from coa1Delta mutant cells, using Mss51 as bait.

9 ant protease and a drug target in cancer, as bait.

10 fferences in 3D distance separation from the bait.

11 screening with the kinase-dead TbPLK as the bait.

12 t two-hybrid screen using twitchin kinase as bait.

13 actions and the consumption frequency of the bait.

14 sing the C-terminus of polycystin-1 (PC1) as bait.

15 the large intracellular loop of GlyRbeta as bait.

16 and NF90 bound a cognate double-stranded RNA bait.

17 ned using the myosin cargo binding domain as bait.

18 sing the ParE subunit of topoisomerase IV as bait.

19 one-hybrid system and the OsRMC promoter as bait.

20 loped, using TRPC4 binding to protein 4.1 as bait.

21 ciprocal pulldown using FLAG-tagged Ycf54 as bait.

22 rmed a yeast 2-hybrid screen using Fbxl22 as bait.

23 fish, making them less likely to respond to bait.

24 cells using a GST-SNX27 fusion construct as bait.

25 ubunit of PKA as interacting with human cTnT bait.

26 -hybrid library and screened it with Me10 as bait.

27 e bait neighborhoods and the distance to the bait.

28 election with glucose-containing insecticide baits.

29 of single B cells using HIV envelope protein baits.

30 5 shot foxes, 142 foxes (81.1%) had consumed baits.

31 -42) and/or monomeric Abeta1-42 (mAbeta1-42) baits.

32 rate and human contact rate with unconsumed baits.

33 ies as the inverse of their use as exogenous baits.

34 pression network for 97 organellar peptidase baits (1742 genes, making 2544 edges).

35 Four types of baits were used: (1) frozen bait; (2) frozen bait and natural chum; (3) fresh fish b

36 was predicted to be low (0.18 per 10 million baits, 95% CI: 0.08, 0.36) when distributed to foxes, bu

37 ncern, 19 times greater (3.35 per 10 million baits, 95% CI: 2.83, 3.98) when distributed to dogs.

38 ategy is attaching to the ligand an affinity bait (AB) and a chemical reporter (CR) group, where the

39 a yeast two-hybrid screen using dysbindin as bait against a cardiac cDNA library to identify the card

40 ing the LUX ARRYHTHMO (LUX) gene promoter as bait against an Arabidopsis TF library.

41 performed yeast two-hybrid screens of 3,305 baits against 3,606 preys ( approximately 70% of the E.

42 The Y2H screen used USP2 as the bait and a prey library consisting of UbVs randomized at

43 using the core promoter region of GluB-1 as bait and cDNA expression libraries prepared from develop

44 behavioural pattern was observed when fresh bait and chum were used, which could increase the potent

45 ormed a yeast two hybrid screen with SR34 as bait and discovered SR45 as a new interactor.

46 d yeast two-hybrid screening using PIF1 as a bait and identified a group of proteins including PIF1 i

47 al in the region immediately surrounding the bait and increasingly lower signals in far-cis and trans

48 t two-hybrid screen using isoform MIG-10A as bait and isolated Abelson-interactor protein-1 (ABI-1).

49 baits were used: (1) frozen bait; (2) frozen bait and natural chum; (3) fresh fish bait; and (4) mack

50 developed a screening method that joins both bait and prey as a convergent fusion into one bacterial

51 emonstrate complex formation by showing that bait and prey molecules are simultaneously trafficked an

52 use of a single protein preparation as both bait and prey thereby halving the number of expression p

53 vitro by pull down experiments using AerR as bait and quantified using microscale thermophoresis.

54 to a soluble telluride, leaving the Ge (one "bait and switch" cycle).

55 organelle-associated reads using a modified "baiting and iterative mapping" approach, conducts de nov

56 iosynthetic enzymes CYP71B15 and CYP71A13 as baits and determined that the camalexin biosynthetic P45

57 do so by running transects of salt and sugar baits and inferring the magnitude of environmental suppl

58 e-proximity interactions between the RC-APEX baits and their respective prey.

59 h protein in two different forms, usually a "bait" and "prey".

60 sed to four different RC components (RC-APEX baits) and 55 unique high-confidence prey were identifie

61 ontent through hybridization with human gDNA baits, and capture-enrichment using gDNA derived from P.

62 social behavior and expose workers to traps, baits, and pesticide applications.

63 Our results suggest that OOR operates via a bait-and-switch mechanism, attracting substrate into the

64 frozen bait and natural chum; (3) fresh fish bait; and (4) mackerel bags.

65 ounting for ant activity (ant usage of sugar baits), ant Na-limitation was next best predicted by pla

66 rary of 'prey' ORFs and surface-immobilized 'bait' antibodies, polypeptides or small-molecular-weight

67 SG temporal disassembly sequence using multi-bait APEX proximity proteomics.

68 Using bioluminescence as bait appears to be highly beneficial for marine bacteria

69 Phytophthora diversity was studied using a baiting approach and metabarcoding (High-Throughput Sequ

70 sing human embryonal carcinoma (EC) cells as bait, approximately 3 x 10(4) potential cell-binding pha

71 m a reversal and entries into the previously baited arm.

72 he removal of carbohydrate, protein and seed baits as a proxy to quantify the contribution that ants,

73 atform can be used to affinity purify tagged baits as well as native cellular proteins and their inte

74 We combined DNA selection by bait-based hybridization followed by Illumina NextSeq re

75 The Scuba7 reduced the proportion of baits being taken by 67%, (from 100% during control tria

76 We suggest that the exploitation of these baited birds was an important adaptation for early farme

77 hases of their analysis, leaving us all with baited breath.

78 are likely to be functionally linked to the baits by calculating the abundance of a given gene withi

79 White sharks spent less time around the baited camera rig when the artificial sound was presente

80 e, than prior estimates from trawl catch and baited camera techniques (152 and 188 individuals km(-2)

81 however, streptavidin plus the biotinylated bait can be completely removed by 3min injections of bio

82 t of the prereplication complex Orc1/Cdc6 as bait captured Poltheta-helicase from the nuclear extract

83 protein microarrays and confirmed by aptamer-baited co-immunoprecipitation (Co-IP) assays.

84 out a yeast two-hybrid screen using a BRCA1 bait composed of amino acids 1 to 1142 and identified BR

85 the only one to use high-density overlapping baits, covers fewer genomic regions than the other platf

86 f the foods, leaving birds to find the still baited cup.

87 es were associated with high fox density and bait delivery in open areas.

88 s targeting raccoons-timing and frequency of bait delivery, width of the ORV zone and proportion of h

89 lyzed using a method that combines human RNA bait-depletion with phi29 DNA polymerase-based multiple

90 Our bait design also enabled phylogenetic assignment of DNA

91 describe a method utilizing biotinylated RNA baits designed specifically for M. tuberculosis DNA to c

92 interactions with the bait, while the frozen bait did not generate a defined behavioural pattern.

93 tion in cultured mammalian cells to a fixed 'bait' DSB.

94 s (DSBs) capable of translocating to defined bait DSBs are enriched around the transcription start si

95 ific genomic Cas9/single-guide RNA-generated bait DSBs.

96 -affinity B cells specific for the antigenic bait during immunization and 2) to minimize subsequent l

97 shed risk variant and that mapped within the bait end of an interaction peak.

98 Transcription factors (TFs) at baited enhancers amplify TF binding at target enhancers,

99 bility of occurrence of prey proteins in the bait experiments relative to the control experiment, whe

100 ons, we developed a rapid method to assemble bait Fc fusion proteins into multivalent complexes using

101 domain, a major collagen-binding domain, as bait for affinity purification of an alpha2beta1 integri

102 -1 Env trimers suitable for use as antigenic bait for bnAb isolation, structural studies, and use as

103 affinity protocol where PAN RNA was used as bait for factors present in BCBL-1 cell nuclear extract

104 The Te atomic layer was bait for Ge deposition, after which the Te was switched

105 ciency virus (HIV) immunogen design and as a bait for isolating anti-HIV antibodies from patient samp

106 Using DSP as bait for screening a protein library, we demonstrate tha

107 elopment included using an aggregated mAb as bait for screening of phage display peptide library and

108 ose as a component of attractive toxic sugar baits for a human-safe approach for mosquito control.

109 are coupled to protein A beads and serve as baits for binding assays with prey proteins extracted fr

110 f customizable internal oligos to be used as baits for gene panel analysis or even probes for large-s

111 aining novel high affinity reactive chemical baits for protein and peptide harvesting, concentration,

112 peaks between putative regulatory elements ("bait fragments") within the captured regions and "target

113 likely to be functionally associated with a 'bait' gene or locus by using relevance metrics.

114 owever, in the absence of glucose-containing bait, glucose-averse (GA) cockroaches have lower perform

115 By using the reagents as bait, >150 putative protein targets were discovered from

116 Ethological analysis showed that the type of bait had a significant effect on the shark's surface beh

117 nditioning of the white sharks, and that all baits have a similar effectiveness for attracting the sh

118 ds to seek alternative food sources, such as baited hooks from longlines, increasing bycatch rates.

119 accomplishing this, such as cell sorting and baiting; however they are time consuming and expensive.

120 ission-blocking vaccine candidate, BBA52, as bait identified an interacting partner in spirochetes-a

121 ing the N-terminal 273 residues of gamma2 as bait identified cardiac troponin I (cTnI) as a putative

122 rification of protein complexes using AN3 as bait identified plant SWITCH/SUCROSE NONFERMENTING (SWI/

123 he core to be captured with high affinity by baits immobilized in the core.

124 his prompted us to use an HSP70 inhibitor as bait in a bioinformatics search for structurally similar

125 In the present study, LMP1 was used as bait in a genome-wide BiFC screen with an enhanced retro

126 Using Sp1-binding motifs as bait in a yeast one-hybrid system, we identified two nov

127 C-terminus of mouse Rpgr(ORF15) was used as bait in a yeast two-hybrid system.

128 ocystis PCC 6803 (Synechocystis) and used as bait in pull-down experiments.

129 s 6803, were FLAG-tagged in vivo and used as bait in separate pulldown experiments.

130 dies, possibly, due to the delayed uptake of bait in which the rabies vaccine was already inactivated

131 Using STK38 as bait in yeast-two-hybrid screens, we discovered STK38 as

132 ylurea receptor (SUR) coiled-coil domains as baits in a 2-hybrid screen against a rat cardiac cDNA li

133 Here, using biotinylated PCR-generated baits in a novel approach, we describe a simple and effi

134 APC10 and CDKD, we tested several additional baits in the different rice tissues and reproducibly ret

135 V origin of plasmid replication (oriP) as a "bait" in lymphoblastoid cells further confirmed contacts

136 rary using the Arabidopsis LDAP3 isoform as 'bait' in an effort to identify other novel LD protein co

137 The RNA bait included 23,941 probes targeting 191 HPV types and

138 Fortunately, negative controls are largely bait independent.

139 protein pull-down experiments using ES7 as a bait indicate that ES7 is a binding hub for a variety of

140 rely on one-versus-all methods in which each bait is sequentially screened against an entire library.

141 The immobilization of the bait is very stable, so that many cycles of prey injecti

142 tal DNA extracted from both soil samples and baiting-leaves.

143 e show that Drosophila can remember a reward-baited location through reinforcement learning and do so

144 Given a set of bait loci and a genomic database defined by the user, th

145 oughout the genome that interact with the 4C bait locus.

146 d by the fact that the immobilization of the bait molecule is usually irreversible; for that reason,

147 ew minutes by immobilizing the corresponding bait molecule on the sensor surface, using one of the co

148 he switchable immobilization of biotinylated bait molecules on a new desthiobiotin surface, using wil

149 dance of a given gene within and outside the bait neighborhoods and the distance to the bait.

150 ons of heparin, suggesting that it bound the bait nonspecifically.

151 rolled trial testing the use of insecticidal bait on cockroach counts and asthma morbidity.

152 This study describes the effect of different baits on the attraction, surface behaviour and condition

153 ly identify interactions in regions near the bait or in regions located in far-cis and trans, but no

154 and tyrosine kinases after treatment using a bait peptide chip array and predicted the corresponding

155 to consume a small piece of local reef fish (bait) placed between the two Scuba7 electrodes with the

156 sponse to the anthropogenic assault of toxic baits, populations of the German cockroach have rapidly

157 Integration of the bait-prey data from the three separate experiments ident

158 Bait-prey junctions are cloned directly from isolated ge

159 The RC-APEX baits produced almost entirely distinct interactomes tha

160 RNAs associated with the bait protein are partially truncated, and the ends of RN

161 ogy to screen a plant cDNA library against a bait protein directly in plants.

162 genes encoding proteins that interact with a bait protein is usually performed in yeast.

163 During CLASH, a tagged bait protein is UV-cross-linked in cell cultures to stab

164 enrichment of an individual protein in every bait protein purification.

165 A approach maps the binding interface of the bait protein used for crosslinking, providing structural

166 extracellular and cytoplasmic regions of a "bait" protein with BioID biotin ligase and identify prox

167 map the centrosome-cilium interface; with 58 bait proteins we generate a protein topology network com

168 eceptor interactions with sensor-immobilized bait proteins, more closely mimicking natural-receptor c

169 t with either, or both, of the Agrobacterium bait proteins, or with CTE.

170 iae) two-hybrid screenings with barley HvROP bait proteins.

171 l plant systems using various conditions and bait proteins.

172 We employ bait RAG-generated breaks in endogenous or ectopically i

173 re and hybridization to large contiguous BAC baits reduces sample and probe hybridization variability

174 aved by host endopeptidases in an accessible bait region.

175 t for differences in signal coverage in near-bait regions, far-cis and trans chromosomes.

176 Hawaiian Islands (MHI) from 2012-2014 using baited remote underwater stereo-video.

177 sing data from more than 15,000 standardized baited remote underwater video stations that were deploy

178 tracking data from 459 individual sharks and baited remote underwater video surveys undertaken in 36

179 Vertebrates were responsible for just 24% of bait removal and invertebrates (including ants) collecti

180 This allowed us to partition bait removal into that taken by vertebrates, non-ant inv

181 e no other organisms compensated to maintain bait removal rate in their absence.

182 There was no compensation in bait removal rate when ants and vertebrates were exclude

183 that ants were responsible for 52% of total bait removal whilst vertebrates and non-ant invertebrate

184 nts carried out 61% of invertebrate-mediated bait removal, with all other invertebrates removing the

185 A yeast-two-hybrid screen with CPRabA5e as bait revealed 13 interacting partner proteins, mainly lo

186 eening of a phage display library with CR as bait revealed a highly basic CR-binding domain (CRB) pre

187 ion of the interactomes of 16 IAC-associated baits revealed a network of 147 proteins with 361 proxim

188 lement (CBE)-flanked loop domains containing bait RSS pairs.

189 raction of the detected PD proteins with the bait RTNLB proteins.

190 ed at least one interactor for 81.4 % of the baits screened for in callus tissue and T1 seedlings.

191 orrhizal fungi at each station using sterile bait seedlings.

192 with biotin, immobilized, and then used as a bait sequence for affinity pull-down of miRNAs.

193 The OsGZF1 protein binds specifically to the bait sequence in yeast and this interaction was confirme

194 We demonstrate that an sxRNA "bait" sequence can be designed to interact with a specif

195 ion with a custom norovirus whole-genome RNA bait set and deep sequenced on the Illumina MiSeq platfo

196 d by whole-exome sequencing with an extended bait set.

197 cturnal, coincident with the availability of baits set by legal hunters.

198 The type of bait showed no significant difference on the effectivene

199 17 different (12 chemically novel) molecular baits showed preferential high affinities (K(D) < 10(-11

200 Natural chum and fresh baits showed short term behavioural patterns constituted

201 mined surveillance data from camera traps at bait sites and records of wild pig removals during this

202 o identified that fidelity and time spent at bait sites by wild pigs was not influenced by increasing

203 Our results revealed that wild pigs used bait sites most during evening and nocturnal periods and

204 increased effort in removing wild pigs using bait sites should be focused during periods of environme

205 Crucially we evaluated the optimal bait size for large fragment libraries and we describe f

206 n sprayable attract-and-kill formulations or bait stations.

207 In conclusion, we developed a cell-bait strategy to unmask renal stem cell binding sites, w

208 Using bait substrates, new hydrolases for sulfate monoesters a

209 affinity-purified PP2A complex with RON3 as bait suggested that RON3 might act in PIN transporter tr

210 ights into the development of novel fire ant baiting systems that can be placed on tree trunks.

211 available norovirus sequences, with multiple baits targeting each position of the genome, which overc

212 mismatches; target enrichment uses multiple baits targeting each position, thus accommodating sequen

213 responsible for fewer interactions with the baited test rigs, and displayed less 'inquisitive' behav

214 uses a panel of custom-designed 120-mer RNA baits that are complementary to all publicly available n

215 matic analysis revealed five clusters of IAC baits that link to common groups of prey, and which ther

216 actions with a single locus of interest (or "bait") that can be important for gene regulation.

217 iched cell wall protein preparation using as bait the NCAP, pumpkin (Cucurbita maxima) PHLOEM PROTEIN

218 ough far less efficient than soluble protein baits, the cell-based capture method identified antibodi

219 can inhibit different proteases cleaving the bait they offer (e.g. serpins, regulating cell death, an

220 Here, we used BAK1 as molecular bait to identify a previously unknown LRR-RLP required f

221 eed extract (Trigonella foenum-graecum) as a bait to identify active ligands that suppress SIRT6 acti

222 and robust targets of MRR and used them as a bait to identify its transcriptional regulators.

223 We then used those 15 genes as bait to identify other correlated genes in the NCI-60 da

224 re, mimicking a resection intermediate, as a bait to identify proteins involved in this process.

225 urated set of viral protein families used as bait to identify viral sequences directly from metagenom

226 Employing C2GnT1 CT as the bait to perform a yeast two-hybrid screen, we have ident

227 in Yersinia pestis), uses monomeric actin as bait to recruit and phosphorylate host actin polymerizat

228 mily GTPases and by using monomeric actin as bait to recruit and phosphorylate host actin-regulating

229 secretin-type G protein-coupled receptors as bait to retrieve potential homologs in the genomes of 15

230 he cytosolic C-terminal region of p22phox as bait to screen a human spleen cDNA library, we identifie

231 s by yeast two-hybrid assay, using GARP as a bait to screen a human Treg cDNA library.

232 a yeast two-hybrid screen with myocardin as bait to search for factors that may regulate the transcr

233 LISA format with immobilized RalGDS-RBD as a bait to selectively capture GTP-bound active Rap1.

234 -hybrid screen was carried out using yjbH as bait to uncover additional substrates or regulators of Y

235 -throughput parallel sequencing and sequence baiting to reconstruct the mitogenomes from 18 type spec

236 uencing libraries commonly uses biotinylated baits to capture the desired sequences.

237 ol compares the genomic neighborhoods of the baits to identify genes that are likely to be functional

238 omic approach using various modified peptide baits to identify reader proteins of various acyl modifi

239 thaliana telomerase reverse transcriptase as baits to screen an Arabidopsis cDNA library encoding pro

240 genes involved in cholesterol metabolism as "bait" to "fish out" (or identify) genes not previously i

241 c polymer nanoparticle (NP) was used as the "bait" to catch an affinity peptide tag.

242 e use of a single intervention, insecticidal bait, to reduce cockroach exposure in the home of childr

243 an unnatural amino acid incorporated in the bait toward a target residue of unknown proteins, here w

244 By using biotinylated RNA baits transcribed from genomic DNA libraries, we are abl

245 set out to develop a simple, low-cost odour-baited trap for collecting C. putoria in the field.

246 ndem pair of caspase-3 cleavage sites, which bait, trap, and disable the active site of caspase-3, th

247 Fuscumol-baited traps also caught significant numbers of another

248 catch of C. capitata than in trimedlure-only-baited traps in Australia, but not in Hawaii where no di

249 emented sterile males were recaptured in MAT baited traps in both the field cages and orchard trials

250 Unexpectedly, we found that trimedlure-baited traps that contained methyl eugenol had x3.1 lowe

251 ly selective mortality of wild males at lure-baited traps while simultaneously releasing sterile male

252 ical role, and the design of efficient sugar-baited traps will all benefit from understanding the mol

253 y deploys a grid of 60,000-100,000 pheromone-baited traps, currently extending from Minnesota to Nort

254 ther demonstrate that geosmin can be used as bait under field conditions, and finally, we show that g

255 We used a baited underwater camera rig to record the behavioural r

256 Using an extensive sampling of 367 stereo baited underwater videos systems, we show modifications

257 To monitor the bait uptake and the serological responses to vaccination

258 In high fox density habitat, bait uptake might be delayed as other food and prey opti

259 Similarly, delayed bait uptake probably occurred in open areas as such area

260 and sugar, over half of the variation in ant bait usage was accounted for by their predictions.

261 on this issue, we designed sequence-capture baits using in silico reconstructed ancestral sequences

262 teractions between proximal proteins and the bait, using single molecule atomic force microscope bind

263 n landfill leachate and colonized cellulose 'baits' via PCR and quantitative PCR (qPCR).

264 oss the Indo-Pacific by using 1,041 midwater baited videos to survey sharks and other pelagic predato

265 In the second experiment, the bait was attached to a small pouch made of either standa

266 ter accounting for activity (ant usage of Na baits) was best predicted by growing season, then ecosys

267 ation sequencing and an enhancer at 8q24 as "bait", we identified genome-wide partners interacting wi

268 o mass spectrometry, with Galpha proteins as bait, we have identified resistant to inhibitors of chol

269 ally processed functional product of nsp1 as bait, we have identified the cellular poly(C)-binding pr

270 reening using the catalytic Sec7 domain as a bait, we identified endophilin as a new partner of EFA6.

271 ns using the purified GluN1-NTD protein as a bait, we identify Protocadherin 7 (PCDH7) as a potential

272 Using pUL103 as bait, we investigated viral and cellular protein-protein

273 ConA), a mannose (Man)-binding protein, as a bait, we narrowed a library of 10(8) glycopeptides to 86

274 Using phosphorylated GST-Bim as bait, we precipitated and identified by mass spectrometr

275 Using DSP as bait, we screened a protein library from mouse odontobla

276 By interactome analysis using THOC5 as bait, we show that upon stimulation with serum THOC5 for

277 Using existing pathway components as baits, we generated by mass spectrometry a high-confiden

278 rized by high latencies to find the previous baited well and higher ir-cell activation in the aforeme

279 n locating and interacting with the previous baited well during the probe test than noncontingent ani

280 Fifty-eight baits were associated with 260 interacting proteins form

281 Four types of baits were used: (1) frozen bait; (2) frozen bait and na

282 Sharks also took more time to take the bait when the device was active (165 +/- 20.40 s vs. 38.

283 ts associated with food (but not water) were baited when the monkey was hungry, and objects associate

284 ts associated with water (but not food) were baited when the monkey was thirsty.

285 The strategic placement of insecticidal bait, which is inexpensive, has low toxicity, and is wid

286 ased number of violent interactions with the bait, while the frozen bait did not generate a defined b

287 cked by preannealing the single-stranded RNA bait with miR-122, indicating that they bind the RNA in

288 trap was a transparent 3L polypropylene box baited with 50 g of fish, with a white opaque lid with c

289 , lightweight 3D-printed mosquito light trap baited with carbon dioxide (CO(2)) in comparison with tw

290 ease Control and Prevention (CDC) light trap baited with CO(2), and the BG Sentinel 2 trap with BG-Lu

291 We presented puzzle boxes, baited with food and scaled to accommodate body size, to

292 task in which only one of two containers was baited with food, the pangolins were able to find the fo

293 Traps baited with human odour plus high contrast visual stimul

294 Currently, traps baited with oviposition semiochemicals play an important

295 f screwworm control programs, utilizes traps baited with rotting liver or a blend of synthetic chemic

296 ts indicated a synergistic response to traps baited with the two component H. halys aggregation phero

297 The camera system was baited with two Periphylla periphylla (Scyphozoa) carcas

298 genes and the corresponding oligonucleotide baits with the highest sequence similarity and demonstra

299 table interactions and tend to result in low bait yield for membrane proteins.

300 in this case achieved up to 100-fold-higher bait yield than previous methods by optimizing lysis, el