ライフサイエンスコーパス: kit

1 Participants in the 2 HIVST arms received 2 kits: 1 at baseline and 1 at 10 weeks.

2 g moieties were evaluated in parallel, and a kit procedure for routine (99m)Tc labeling was developed

3 At first, we have designed a kit combining the novel fluorescence turn-on sensors for

4 e BRAF delayed melanoma onset, but only in a kit-dependent manner.

5 microplates, that has been developed into a kit suitable for HT work.

6 To address this question, we introduced a kit(lf) mutation into a strain of Tg(mitfa:BRAF(V600E));

7 tings, the device can be used as a part of a kit (containing the device, a fixed-volume capillary, a

8 OMT(-/-) and C57BL/6J mice were made using a kit from BIOCRATES.

9 r crosstalk, with the ability to assemble a "kit" of directional instructions made up of different mo

10 asured in serum samples with the AbsoluteIDQ kit p150 (Biocrates) following a targeted metabolomics a

11 th three different GBS antigen agglutination kits, PathoDx (Remel) (93%), Prolex (Pro-Lab Diagnostics

12 vitro transcription by T7 RNA polymerase and kit-based purification provides a cost-effective and fas

13 inhibitory activity using the glucose assay kit was developed.

14 l sandwich enzyme-linked immunosorbent assay kit.

15 l sandwich enzyme-linked immunosorbent assay kit.

16 sured using an sEH inhibitor screening assay kit.

17 hod 32-40), using the resistant starch assay kit) of raw brown lentil starch (BLS) increased signific

18 Five commercially available assay kits were tested on the same protein sample with the add

19 fluorescence staining and colorimetric assay kits.

20 er of commercially available enzymatic assay kits utilize NADH in their detection, this discovery wil

21 commercial enzyme-linked immunosorbent assay kits for immunoglobulin M/immunoglobulin G antibodies to

22 hich we compared with commercially available kits and verified with seroconversion panels, the WHO HB

23 and low reactivity of commercially available kits have been observed with regard to ELISA and PCR met

24 l a brief revision of commercially available kits is also included in this review.

25 serum sample by using commercially available kits.

26 s were measured using commercially available kits.

27 differ markedly between currently available kits.

28 ncy of three subtractive hybridization-based kits in depleting rRNA from samples derived from biofilm

29 nts is limited by a weak correlation between kit results caused by differences in the selectivity of

30 present in the samples were observed between kits.

31 rom 4h using commercially available bioassay kits to 10min using the MAB technique.

32 pared to the commercially available bioassay kits.

33 ommercially available gold standard bioassay kits run at room temperature.

34 Both kits show significantly lower analytical sensitivity on

35 a test kit to their male partner or use both kits for testing as a couple.

36 c progenitors, including lineage(-)Sca-1(+)c-kit(+) (LSK), common myeloid progenitor, and granulocyte

37 One of the two exon 11 c-kit mutations in synchronous adenocarcinomas with GISTs

38 uencing analysis demonstrated that exon 11 c-kit mutations were present in two of six synchronous tum

39 e uniformly distributed in the BM, and all c-kit(+) progenitor cells were adjacent to Gr1(+) myeloid

40 different between c-kit D816V-positive and c-kit D816V-negative patients, while 11beta-prostaglandinF

41 Previous work in Il3-deficient and c-kit mutant Kit(W/W-v) mice indicated that interleukin-3

42 -derived mesenchymal stem cells (MSCs) and c-kit(+) cardiac stem cells (CSCs) improve left ventricula

43 ry NMH was significantly different between c-kit D816V-positive and c-kit D816V-negative patients, wh

44 expressed by HSCs, and at lower levels by c-kit(+) hematopoietic progenitors, megakaryocytes, and Le

45 Although cardiac c-kit(+) cells are being tested in clinical trials, the ci

46 t findings suggest that endogenous cardiac c-kit(+) cells rarely contribute cardiomyocytes to the adu

47 Previously, cardiac c-kit(+) cells were reported to be CSCs with a potential t

48 urther insights into the nature of cardiac c-kit(+) cells.

49 CRTh2(+)ILC2 differentially express CD117 (c-kit receptor), some ILC2 surface phenotypes are unstable

50 The tumor cells were positive for CD117 (c-kit) (Fig 1B) and DOG-1(Fig 1C).

51 +)c-kit(+)MPs), and basophil MPs (CD203c(+)c-kit(-)MPs).

52 Single-cell sequencing of cardiac CD45(-)c-kit(+) cells showed innate heterogeneity, indicative of

53 e-immunofluorescence staining, we detected c-kit (a marker of cell transdifferentiation) positive duc

54 ated mast cell MPs (CD137(+) FcepsilonRI(+)c-kit(+)MPs) were significantly increased in NLFs of contr

55 high-affinity IgE receptor [FcepsilonRI](+)c-kit(+)MPs), and basophil MPs (CD203c(+)c-kit(-)MPs).

56 s, and rare cardiomyocytes originated from c-kit positive progenitors.

57 erall rate of cardiomyocyte formation from c-kit(+) cells is still below clinically relevant levels,

58 referentially generate cardiomyocytes from c-kit(+) cells.

59 The distribution of alpha-catulin-GFP(+)c-kit(+) cells indicated that HSCs were more common in cen

60 tically, doxorubicin-induced DNA damage in c-kit(+) cells resulted in expression of p53.

61 overload resulted in a modest increase in c-kit-derived cardiomyocytes, with significant increases i

62 lization of p53 was sufficient to increase c-kit-derived cardiomyocyte differentiation.

63 uced acute cardiotoxicity did not increase c-kit-derived endothelial cell fates but instead induced c

64 After acute cardiac injury, c-kit(+) cells retain their endothelial identity and do no

65 Instead, c-kit predominantly labels a cardiac endothelial cell popu

66 We isolated c-kit(+) cells from young (3 months) and aged (24 months)

67 on supported the increase in marrow lin(-) c-kit(+) Sca-1(+) cells.

68 ration inhibited this activation of lin(-) c-kit(+) Sca-1(+) cells.

69 sed a remarkable increase in marrow lin(-) c-kit(+) Sca-1(+) cells.

70 ic stem cells (CD150(+)/CD48(-)/Lineage(-)/c-kit(+)/Sca-1(+)) identified a large number of differenti

71 NK cells do not express the early markers c-kit and IL-7Ralpha, nor killer cell Ig-like receptors or

72 The 22-mer c-kit promoter sequence folds into a parallel-stranded qua

73 the existence of vascular and mesenchymal c-kit(+) cells in normal hearts.

74 mast cell-deficient mice that have normal c-kit ("Hello Kitty" and MasTRECK mice) confirmed prior wo

75 ABSTRACT: Therapeutic use of c-kit(+) cardiac progenitor cells (CPCs) is being evaluate

76 ical analyses confirmed the recruitment of c-kit(+) cells as well as a reduced degree of apoptosis 1

77 Here we test the lineage potential of c-kit(+) cells by inducible genetic lineage tracing.

78 that determine lineage differentiation of c-kit(+) cells in vivo are unknown.

79 cal stimuli induce different cell fates of c-kit(+) cells in vivo.

80 show that p53 is central to the ability of c-kit(+) cells to adopt cardiomyocyte fates, which could l

81 sequencing and genetic lineage tracing of c-kit(+) cells to determine whether various pathological s

82 w hypocellularity and the disappearance of c-kit(+) cells.

83 entially affect the eventual cell fates of c-kit(+) cells.

84 stimuli would result in different fates of c-kit(+) cells.

85 l attention to the clinical application of c-kit(+) stem cells as lung epithelial progenitors for the

86 We identified a novel population of c-kit-negative reparative cardiac cells (SA CMCs) that can

87 ction of aged stem cells and in particular c-kit(+) cardiac progenitor cells (CPCs).

88 eviously reported that the c-kit-positive (c-kit(POS)) cells isolated from slowly adhering (SA) but n

89 Purified (c-kit+/sca1+/lin-) HSCs were infused repeatedly into mice

90 ble to suppress stem cell factor receptor (c-kit or CD117) gene expression by interacting with a newl

91 ved hematopoietic stem cells reconstituted c-kit but not MAT in Kit(W/W-v) mice.

92 The residual c-kit(pos) cells found in the adult heart are probably of

93 ntages, appearing to be more suitable than c-kit(POS) cardiac progenitor cells for widespread clinica

94 tiple reporter genes in mice, we find that c-kit expression rarely co-localizes with the expression o

95 Thus, our work strongly suggests that c-kit(+) cells in the murine heart are endothelial cells a

96 ng with a newly identified silencer in the c-kit gene.

97 By targeting the c-kit locus with multiple reporter genes in mice, we find

98 The authors previously reported that the c-kit-positive (c-kit(POS)) cells isolated from slowly adh

99 hether adherence to plastic alone, without c-kit sorting, was sufficient to isolate reparative CMCs.

100 elect Human all Exon 51 Mb version 5 capture kit.

101 updated version of the Rosco Neo-Rapid Carb kit, which does not require the preparation of imipenem

102 ologic advances are leading to point-of-care kits that incorporate nucleic acid-based assays, includi

103 A one-use CEC kit was developed, where the fast reaction was identifie

104 ll Genomiphi, and Qiagen REPLI-g single cell kits were used to test identical sonicate fluid samples.

105 IL-1RL1-a; and 3) using non-serum certified kits may lead to spurious findings.

106 esize human calmodulin (CaM) by using a CFPS kit and prove the structural integrity and the full func

107 ates from the Zymo, Qiagen, and ChargeSwitch kits.

108 Negative Pronto Dry and CLOtest kits may be reused in a low prevalence setting where cos

109 Reused CLOtest kits have better accuracy than reused Pronto Dry tests.

110 , paradoxically, the cardiogenic fate of CNC(kit) is regulated by bone morphogenetic protein antagoni

111 neates cardiac neural crest progenitors (CNC(kit)).

112 ddition of (68)Ga generator eluate to a cold kit.

113 tion from a Good Manufacturing Practice cold kit may enable rapid adoption.

114 Cold kits are produced in some countries, and therapeutic age

115 ed by reference method (Enzymic colorimetric kit method) and the present biosensor.

116 esting can be useful in CM, and a commercial kit is available.

117 ustom mtDNA-specific primers or a commercial kit, and minimizes the contamination of nuclear encoded

118 ison of results with those from a commercial kit.

119 cording to the directions for the commercial kit, although further serial dilutions of the standard i

120 Available commercial kits are often unsatisfactory and require modifications

121 oratory instrumentation employing commercial kits.

122 Easy-to-use commercial kits for harvesting exosomes are now widely used, but th

123 We used commercial kits to analyze serum levels of hyaluronic acid, tissue

124 average) was lower than that with commercial kits (23%).

125 of an ultrastable biomolecular construction kit for the assembly of filamentous proteins into geomet

126 ts at RWJUH were provided with blood culture kits containing either chlorhexidine (CH) or iodine tinc

127 es (ROS) production was measured using DCFDA kit.

128 e, facility delivery, use of a safe delivery kit, hand washing by the birth attendant prior to delive

129 liveries, including the use of safe delivery kits (odds ratio [OR] 2.92, 95% CI 2.02-4.22; I2 = 63.7%

130 own to vary based on the antibody, detection kit brand, antigen retrieval method, and clinically defi

131 presence of HP using stool antigen detection kit.

132 ersion 2 [V2]) and Nipro NTM+MDRTB detection kit 2 (referred to as Nipro), to Hain V1.

133 tools via an intuitive software development kit.

134 which is routinely used in these diagnostic kits is Histidine-rich protein-2; a protein synthesized

135 2 (tTG) antibodies performed with different kits but all corresponding to those recommended by ESPGH

136 through pairwise comparison within different kits.

137 The attraction with DIY kits is the simplification of the intervening steps goin

138 Drug kits were coded, providing masking to treatment assignme

139 The Zaire Ebolavirus kit is based on the Filovirus Screen kit but was optimiz

140 1 was measured by human sVEGFR1/sFlt-1 ELISA kit.

141 Circulating ZAG was determined with an ELISA kit.

142 n the enzyme, gluten grain source, and ELISA kit used, measured gluten content was significantly redu

143 biosensors and commercially available ELISA kit (Kinesis DX).

144 e results using commercially available ELISA kit for CXCL5 detection.

145 The Biochain ELISA kit for Human Hepatitis C Virus was used for antibody as

146 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients.

147 a detection enzyme with any commercial ELISA kit with a wide range of concentration of antigens.

148 h those obtained by using a commercial ELISA kit.

149 nt with those provided by a commercial ELISA kit.

150 ing both the aptasensor and commercial ELISA kit.

151 developed biosensor and the commercial ELISA kit.

152 with those registered with competitive ELISA kit.

153 rcially available osteocalcin sandwich ELISA kit.

154 d correlation within the limits of the ELISA kit.

155 We evaluated four IL-33 ELISA kits, aiming to determine a robust and reproducible appr

156 rnative for the commercially available ELISA kits for PSA determination.

157 antibody using commercially available ELISA kits.

158 shorter assay time than the available ELISA kits.

159 Commercial ELISA kits are known to give false-positive results for OTA co

160 d, which were comparable to commercial ELISA kits using specialized equipment.

161 n blood is largely based on commercial ELISA kits which are based on polyclonal antibodies (pAbs) not

162 ne as a detection system in commercial ELISA kits.

163 Commercialized ELISA kits for Ara h 1 and Ara h 2 report limits of detection

164 Three of the MAC-ELISA kits and 1 indirect immunofluorescence kit had comparabl

165 pplicability of two commercial mustard ELISA kits (Mustard ELISA Kit-specific and Mustard ELISA Kit-t

166 d with other previous immunosensors or ELISA kits.

167 The ELISA kits exhibited variations in gluten quantitation dependi

168 The ELISA kits performed well in detecting allergens in the raw sa

169 ysis on gluten quantitation by various ELISA kits was evaluated.

170 ed with respect to those obtained with ELISA kits.

171 Patients should carry an emergency kit containing an adrenaline autoinjector, H1 -antihista

172 ior WGA using an NEBNext Ultra II paired-end kit, which requires a very small amount of input DNA.

173 ls, were evaluated using a target enrichment kit and sample-multiplexed nextgen sequencing.

174 is paper, the effectiveness of two enzymatic kits in detecting residual lactose in lactose-free milk

175 d with the Agilent SureSelect Human All Exon kit, sequenced on the Illumina Hiseq 2000, and the resul

176 ed on the BD Max using the BD Max extraction kit ExK-DNA-1 test strip and a master mix prepared by Bi

177 s improved by applying a specific extraction kit.

178 xtracted using two commercial DNA extraction kits, we confirmed that dPCR could discern individual co

179 onal silica-based solid-phase RNA extraction kits.

180 s somewhat more sensitive than the Filovirus kit.

181 the number of invitations sent in 2014, FIT kits returned, and colonoscopies performed.

182 ly available Etest((R)) (Biomerieux, France) kit.

183 Tumors from kit(lf) animals were more invasive and had higher RAS/MA

184 splacement amplification (MDA-Qiagen REPLI-g kit) and the hybrid or modified PCR-based method (Sigma/

185 Plex kit but highly variable for the REPLI-g kit.

186 igher in samples amplified using the REPLI-g kit.

187 GenomePlex kit) in FFPE normal and tumor tissue specimens.

188 amples, which was minimal for the GenomePlex kit but highly variable for the REPLI-g kit.

189 al in samples amplified using the GenomePlex kit, but they were statistically significantly higher in

190 m, and identified using the Hain(R) Genotype kits.

191 sequenced using the Trugene HIV-1 genotyping kit.

192 was similar to that of a commercial glucose kit, and (ii) in vivo dynamic monitoring of the extracel

193 We devised a Global MST Enrichment (GME) kit to enrich and nextgen sequence 2 colorectal cell lin

194 (68)Ga labeling of peptides using GMP kits was performed in 15-20 min, and the total productio

195 ent volunteer-counsellors offered oral HIVST kits (OraQuick ADVANCE Rapid HIV-1/2 Antibody Test) to a

196 linical samples using the HeavyPeptide IGNIS kit which establishes a 6-point calibration curve and de

197 We have optimised the IGNIS kit to quantify APO-F as a NAFLD biomarker in serum usin

198 sed to generate a sensitive immunodiagnostic kit, which offers the potential for a highly specific cl

199 ELISA kits and 1 indirect immunofluorescence kit had comparable performance to the reference assays.

200 Melanoma onset was accelerated in kit(lf); Tg(mitfa:BRAF(V600E)); p53(lf) fish.

201 those trained with a video self-instruction kit (VSI; with manikin).

202 samples by GIDAGEN Multi-fast DNA isolation kit.

203 This LFIA, coupled to EVs isolation kits, could become a rapid and useful tool for the point

204 nsing platform, combined amino acid labeling kit and a double-generation gold nanoparticle (DG-AuNP)

205 Second, the labeling kit was used to examine the DV binding to the CLEC5A-coa

206 kines and chemokines using a 17-plex Luminex kit or enzyme-linked immunosorbent assay.

207 hing for methylated DNA with the MethylMiner kit and performing next-generation sequencing (MBD-Seq)

208 6 mice were immunized with the Hooke lab MOG kit, sacrificed at the peak of the disease and their spi

209 ielded >/=0.2 ng/mul of DNA for 90% (MolYsis kit) and 83% (saline wash) of positive MGIT cultures.

210 rent commercial multiple reaction monitoring kits and an antibody-based multiplexing kit were used to

211 d between the 2 multiple reaction monitoring kits, but some of the multiple reaction monitoring-based

212 uantitative RT-PCR and ELISA and a multiplex kit for IL-35 and IL-12, respectively.

213 ring kits and an antibody-based multiplexing kit were used to compare the apolipoprotein measurements

214 Nase, and the Wizard Magnetic and Nucleospin kits.

215 There was no evidence that one kit was better than another.

216 but a common protocol (the AbsoluteIDQ p180 kit) for the measurement of 189 metabolites via liquid c

217 e applications - a standard well-based paper kit and a portable layer-by-layer stick kit.

218 CR results (RealStar Filovirus Screen RT-PCR kit 1.0; altona Diagnostics GmbH, Hamburg, Germany) for

219 the derived RealStar Zaire Ebolavirus RT-PCR kit were validated using in vitro transcripts, supernata

220 scription-polymerase chain reaction (RT-PCR) kit and a malaria rapid diagnostic test, respectively.

221 scription-polymerase chain reaction (RT-PCR) kit and the derived RealStar Zaire Ebolavirus RT-PCR kit

222 scription-polymerase chain reaction (RT-PCR) kits are available commercially, but validity data are l

223 round contamination, an isolator column (PFC kit) was installed in between eluent mixer and injector

224 se of the Nextera XT DNA library preparation kit produced significantly better results than other pre

225 oach, the Nextera XT DNA library preparation kit, for library preparation.

226 enchmarking of different library preparation kits (standard poly-A versus total RNA with Ribozero dep

227 ation in popular commercial DNA purification kits, we employed a novel high-speed atomic force micros

228 nostics recently introduced the IS6110-PvuII kit for semiautomated typing of Mycobacterium tuberculos

229 Qiagen kits tested positive in the fluorescence assay but negat

230 binant HEV-capsid protein in the QuantiFERON kit.

231 eta=0.98, p<0.0001) whereas My Bio Source(R) kit results were not correlated with those provided by L

232 e PCR for 33 respiratory pathogens (FTD((R)) kit).

233 rator into a lyophilized radiopharmaceutical kit in 1 step without manipulation.

234 Spent RDT kits and prepared blood slides were collected and interp

235 he validation of other platforms and reagent kits.

236 Because of a straightforward and reliable kit production, (99m)Tc-PSMA-I&S represents a cost-effec

237 A robust and reliable kit-labeling procedure was established, allowing the pre

238 Data generated using the total RNA kit had more signal for introns and various RNA classes

239 We provided pet owners with a sampling kit and instructional video to swab the skin of their an

240 s Institute, and the Rosco Rapid Carb Screen kit.

241 lavirus kit is based on the Filovirus Screen kit but was optimized for detection of EBOV.

242 The Filovirus Screen kit detected EBOV, Sudan virus, Tai Forest virus, Bundib

243 The Filovirus Screen kit detects all human-pathogenic filoviruses with good a

244 clinical sensitivity of the Filovirus Screen kit to diagnose EVD at an early stage.

245 , and micro-RNA using Qubit high-sensitivity kits.

246 tro diagnostic MALDI Sepsityper (Sepsityper) kit has the potential for standardization and clinical r

247 e many sequencing services and off-the-shelf kits suffer from slow turnaround, inefficient capture of

248 For snail kites, our method reveals substantial differences in mov

249 ulation structure (i.e. modularity) in snail kites.

250 cant modularity in annual dispersal of snail kites (all adults, males only, females only, and juvenil

251 umor regions of FFPE tissues where the SP263 kit does not.

252 equence-independent, and requires no special kits, enzymes or proprietary bacteria, which will allow

253 nsor can also be used as an economical spray kit to directly spot the explosives by naked eyes, imply

254 Here, we present cl-dash, a complete starter kit for setting up such an environment.

255 nced by the availability of a simple, 1-step kit-based labeling process.

256 SMA, has a simplified design for single-step kit-based radiolabeling.

257 aper kit and a portable layer-by-layer stick kit.

258 obtained using AOAC-approved ELISA or strip kits, as the Cohen's kappa coefficients for both compari

259 that occurs during PPB, a dietary supplement kit consisting of monoamine precursor amino acids and di

260 sting modality enables users to order a test kit from a virtual service (via a website or app), colle

261 se them, and encouraged to distribute a test kit to their male partner or use both kits for testing a

262 Using Avellino gene test kit, the TGFBI mutation detection was performed on DNA s

263 on of the Corgenix ReEBOV Antigen Rapid Test kit.

264 sing the cutoff levels suggested by the test kit manufacturers.

265 nd Toxoplasma commercial IgM diagnostic test kits can yield a number of false-positive results.

266 oup were given two oral-fluid-based HIV test kits, instructed on how to use them, and encouraged to d

267 ogram or (2) the manufacturer of the testing kit by conducting additional tests as part of an effort

268 as part of an effort to improve the testing kit.

269 d the build-out of instrumentation and tests kits for POC deployment.

270 The kit has been validated according to industry analytical

271 ike traditional microscopic diagnosis, these kits rely on the detection of antigens specific to malar

272 This kit has the technical characteristics to be employed as

273 Consequently, this kit can be used to light-on single DV spot both in solut

274 filled tube, a syringe, and a dropper); this kit would cost $0.50 when produced in large scale (>10

275 Advantages of this kit are that emission on-off switching can increase the

276 low plasma viral load (P < .02), and time to kit expiration (P < .01).

277 We demonstrated that a tool kit of multiple probes can be used to label extracellula

278 pproaches to bolster the vector-control tool kit.

279 es are a component of the developmental tool kit for the vertebrate vascular system.

280 ady expansion of the chlamydial genetic tool kit, there are still roads left to be traveled.

281 our findings greatly expand the limited tool kit available to study pathogenesis and host response to

282 ther, these methods provide a practical tool kit for those wanting to use SMALPs to study membrane pr

283 cal testing as an important part of the tool kit.

284 e of a well-defined medicinal chemistry tool-kit focused on PMTs, most current inhibitors were identi

285 Blinded treatment kits were used to achieve masking of patients and staff.

286 Rapid, ultrasensitive diagnostic/triaging kits for early detection of malarial parasites are criti

287 ce assay while the WGA results for these two kits were ambiguous.

288 or the microsyringe protocol and the one-use kit both displayed data consistent with pseudo-first-ord

289 The single-use kits developed are low cost, easy and fast to manufactur

290 r for ICCs-and consequent up-regulation of v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homo

291 VCF-kit adds essential utilities to process and analyze VCF

292 into a command-line based utility named VCF-kit.

293 ated using the Qiagen QIAamp UltraSens Virus kit, followed by real-time reverse transcription polymer

294 These findings highlight the impact that WGA kit selection can have on metagenomic analysis of low-bi

295 on the application, background DNA from WGA kits can be problematic.

296 Three WGA kits were tested for their utility in a metagenomics app

297 r imaging with PET that can be produced with kits are currently in the spotlight of radiopharmacy and

298 Finally, we demonstrate that the Ribo-Zero kit also exhibited the highest efficiency when P. aerugi

299 for the three procedures, with the Ribo-Zero kit yielding the highest degree of rRNA depletion, which

300 Eluates from the Zymo kits also tested positive for DNA in fluorescent interca