ライフサイエンスコーパス: kit

1 kits at enrollment and could receive 2 to 4 kits delivered through express mail every 3 months for 1

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

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

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

5 (68)Ga-NeoBOMB1 was prepared using a kit procedure with a licensed (68)Ge/(68)Ga generator.

6 ng for selective testing of samples within a kit, where only the most probative samples are tested.

7 pite the larger design region of the Agilent kit, we find that the Illumina kit performs better in te

8 animals died of apparent infection, and all kits were resorbed in another animal that did not die.

9 itutes as well as the commercial devices and kits developed by companies for the detection of SARS-Co

10 al materials (radioisotopes, generators, and kits) were reported, especially for (99m)Tc/(99)Mo gener

11 ed on covariates gleaned from sexual assault kit questionnaires) which samples are most probative.

12 hough the backlog of untested sexual assault kits in the United States is starting to be addressed, m

13 ured using the Diazyme Total Bile Acid Assay kit.

14 surements using a commercial enzymatic assay kit.

15 ing a commercially available enzymatic assay kit.

16 cate within the TaqMan gene Expression Assay kit.

17 l sandwich enzyme-linked immunosorbent assay kit.

18 en different primer-probe sets and one assay kit.

19 fluorescence staining and colorimetric assay kits.

20 rmaldehyde and creatinine fluorometric assay kits.

21 d FVIII-SQ was observed across various assay kits and clinical laboratories, suggesting that intrinsi

22 tomatic biochemical analyzer with associated kits.

23 Several ATP kit assays are already commercially available but an use

24 was extracted with a commercially available kit and detected via real-time PCR IS6110 amplification.

25 were assessed with a commercially available kit.

26 pared with those of a commercially available kit.

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

28 The commercially available kits commonly require at least 100 muL of a sample at 1

29 e performances of two commercially available kits for Whole Genome Amplification (WGA), PicoPLEX and

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

31 s were measured using commercially available kits.

32 differ markedly between currently available kits.

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

34 the above concepts and methods for Biocrates kits and other target data sets and creates a comprehens

35 for the generation of ready-to-use biomarker kits for clinical applications as it is compatible with

36 promote human-aggression by raptorial Black kites Milvus migrans in the 16-millions inhabitants mega

37 Both kits achieved the radiochemical purities of > 95%.

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

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

40 quantitative real-time PCR for chymase and c-kit.

41 2KO) We found that NOD/SCID/gamma(C) (-/-) c-kit(+) mice engrafted with human tissues 1 day after bir

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

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

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

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

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

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

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

49 We performed RNA sequencing from c-kit+ progenitor cells isolated from 32 patients, includi

50 age-dependent reparative effects of human c-kit+ progenitor cells (hCPCs) in a rat model of juvenile

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

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

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

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

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

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

57 ) cells is also necessary to maintain many c-kit(+)-restricted hematopoietic progenitors.

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

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

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

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

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

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

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

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

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

67 ations with KI and KO, or imprecise KI, of c-kit.

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

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

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

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

72 Transient activation of the c-kit receptor induces the expression of growth factors an

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

74 ne production of SCF activates a transient c-kit receptor in keratinocytes.

75 we may be able to identify patients whose c-kit+ progenitor cells exceed or underperform expectation

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

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

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

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

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

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

82 automated synthesis modules, a sterile cold kit was recently introduced.

83 ctivity was synthesized using a sterile cold kit.

84 nt differences in image quality between cold kits and synthesis modules were found (P = 0.13), althou

85 practical large-scale production, and a cold-kit formulation would improve the spontaneous availabili

86 ction of (18)F-FAPI-74 or decentralized cold-kit labeling of (68)Ga-FAPI-74 allows flexible routine u

87 ome finger-prick dried blood spot collection kit and an analysis method.

88 isruptions affect availability of collection kits.

89 ontrol provided in a commercial colorimetric kit for m6A-RNA quantification.

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

91 t between the OFUS system and the commercial kit was obtained.

92 Commercial kits are now available which use carefully calibrated an

93 Available commercial kits are often unsatisfactory and require modifications

94 -effective compared to equivalent commercial kits suitable for detecting adulterant pork levels in me

95 for ochratoxin A (OTA), including commercial kits, show limitations to robustly determine this mycoto

96 rse transcription PCR), with many commercial kits now available for this purpose.

97 rnals or divided between numerous commercial kits which prevents optimal connectivity between compani

98 testing since the introduction of commercial kits in the mid-1990s.

99 hich no established assays and/or commercial kits are available (e.g., Ascaris EVs), thus making it a

100 ormance was comparable with other commercial kits demonstrating: repeatability and reproducibility; p

101 The commercial kits/analytical methods based-sensing strategies have al

102 d in conjunction with widely used commercial kits.

103 lease assay were successfully measured by DA kits, and the aptasensor sensing properties were compare

104 Using the DrosDel deficiency kit, we identified 3 out of 346 deficiency lines that en

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

106 presence of HP using stool antigen detection kit.

107 his report, the current SARS-CoV-2 detection kits, exclusively the ones that were issued an "Emergenc

108 uture development of point-of-care detection kits for cancer diagnosis in a clinical setting.

109 ally available G-CSF and PEG ELISA detection kits have different capacities to detect pegfilgrastim a

110 tools via an intuitive software development kit.

111 Here we describe a diagnostic kit to enable analysis of bacterial blight in the field

112 designing a rapid electrochemical diagnostic kit composed of fixed/screen printed electrodes that can

113 d aPL were measured with clinical diagnostic kits.

114 y available liquid lenses(8) and diagnostics kits(9,10).

115 2 (tTG) antibodies performed with different kits but all corresponding to those recommended by ESPGH

116 through pairwise comparison within different kits.

117 y run time of the Simplexa Bordetella Direct kit are favorable compared to those of other commercial

118 In summary, the Simplexa Bordetella Direct kit has a performance comparable to those of other molec

119 erformance of the Simplexa Bordetella Direct kit to those of other molecular assays in detecting and

120 revealed that the Simplexa Bordetella Direct kit was 100% specific.

121 vide exhaustive coverage statistics for each kit to aid the assessment of their suitability and provi

122 that selects which samples to test from each kit to maximize the Combined DNA Index System (CODIS) yi

123 massive population of migratory Black-eared kites wintering around the megacity of Delhi-India, whic

124 e bottom up, and next-generation educational kits.

125 in agreement with those provided by an ELISA kit and allow discrimination between positive and negati

126 levels using a commercially available ELISA kit.

127 easured using a commercially available ELISA kit.

128 ntified using a commercially available ELISA kit.

129 oped sensing platform and a commercial ELISA kit for validation.

130 of aptasensor compared to a commercial ELISA kit of SEB detection proved the superior performance of

131 red wine, while whereas the commercial ELISA kit was instead unable to detect egg white in the same s

132 dose for C. jejuni while a commercial ELISA kit was unable to detect the bacterium.

133 h those obtained by using a commercial ELISA kit.

134 d using two separate ScheBo-Biotech-AG ELISA kits for stool and plasma samples.

135 ventional NS1 antigen and IgM antibody ELISA kits.

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

137 findings suggest that most commercial ELISA kits may not reliably quantify peanut present in dark ro

138 compared side-by-side with commercial ELISA kits where the total assay time is reduced 15-fold, from

139 ing was evaluated using two commercial ELISA kits: Veratox(R) for peanut allergen and peanut ELISA fr

140 ts comparable to commercial diagnostic ELISA kits at a substantially reduced cost and reaction time.

141 otein assays and six commercial peanut ELISA kits, respectively.

142 erformance to commercial single-target ELISA kits as well as shorter assay time, less consumption, an

143 ed with respect to those obtained with ELISA kits.

144 le enzyme-linked immunosorbent assay (ELISA) kits and, therefore, this hinders progress in the discov

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

146 accelerate progress in the field, the entire kit, as described, is available through Addgene at minim

147 t-seq2 or the single-cell 5' gene expression kit from 10x, extending its utility to single-cell RNA-s

148 MS and QuEChERS(TM) multiresidue-extraction kit.

149 the RT-LAMP assay without an RNA extraction kit.

150 mmercially available nucleic acid extraction kits (i.e., from Qiagen) and a simple heat and detergent

151 We found that different extraction kits favour some species and bias against others.

152 tic method and two commercial DNA extraction kits.

153 gents such as PCR primers and RNA extraction kits are at critical shortages.

154 he current global shortage of RNA extraction kits has caused a severe bottleneck to COVID-19 testing.

155 ple, economical, and portable piece of field kit for on-site monitoring of tetracyclines in a variety

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

157 ening outreach was performed with mailed FIT kits.

158 was rated as excellent by the observers for kits than for modules (45% vs. 34%).

159 Here we compared the efficacy of four kits from Invitrogen, 101Bio, Wako and iZON along with c

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

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

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

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

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

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

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

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

168 ance over 5 common STRs with the GlobalFiler kit.

169 at determined with a commercial ELISA gluten kit.

170 ge in a dense two-dimensional system of hard kites that are rotationally asymmetric and have opposite

171 pha, we apply LPC-NPP analysis to other hard kites for 54 degrees <= alpha <= 144 degrees .

172 ; the second and third arms provided 2 HIVST kits along with a conditional fixed financial incentive

173 f $3 or $10; the fourth arm provided 2 HIVST kits and a 10% chance of receiving $30 in a lottery; and

174 lottery; and the fifth arm provided 2 HIVST kits and a phone call reminder for the women's partners.

175 s: the first arm provided women with 2 HIVST kits for their partners; the second and third arms provi

176 rovided with 2 free finger-prick-based HIVST kits at enrollment and could receive 2 to 4 kits deliver

177 They were encouraged to distribute HIVST kits to their sexual partners.

178 is study, we found that providing free HIVST kits significantly increased testing frequency among Chi

179 Our in-house kit compares favorably with a commercial product used fo

180 The g-iELISA kit is available for evaluation in reference laboratorie

181 cZyme VZV glycoprotein (VZVgp) low-level IgG kit (The Binding Site Ltd., Birmingham, UK) using the Wo

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

183 f the Agilent kit, we find that the Illumina kit performs better in terms of gene coverage, as well a

184 digests were >80% for the commercial Fe-IMAC kit and the Strata X-AW sorbent.

185 nd it was found to be better for the Fe-IMAC kit.

186 commercialized chemiluminescence immunoassay kits in clinical serum detection.

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

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

189 The Invitrogen kit gave the highest yield but the preparation showed br

190 hils were purified with a specific isolation kit, and phenotypic and functional studies were performe

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

192 the mammalian Expi293F amino acid labelling kit is suitable for preparation of multi-milligram quant

193 otypic serotyping, we used a 13-valent latex kit (Statens Serum Institut [SSI], Denmark).

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

195 ted infections, the Qiagen UCP pathogen mini kit provided the highest ratio of N. gonorrhoeae to huma

196 g TRIZOL kit (Invitrogen), Plant RNeasy mini kit (Qiagen), Furtado (2014) method, and CTAB-LiCl metho

197 d on the detection principle, a miniaturized kit [20.0 mm (L) x 20.0 mm (W) x 2.15 mm (H)] was develo

198 Thus, the MoChlo kit represents a valuable tool for fast and flexible des

199 ry and syntax of the Plant Golden Gate MoClo kit, we have developed a versatile system called CyanoGa

200 6 mice were immunized with the Hooke lab MOG kit, sacrificed at the peak of the disease and their spi

201 ter a single experiment using the monitoring kit showing how efficiencies in the lab can be gained wi

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

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

204 Only the Morinaga kit showed sufficient sensitivity to detect peanut at lo

205 5 and 28 +/- 2 with the Veratox and Morinaga kits, respectively.

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

207 -17A, IL-17C and IL-22 using ELISA multiplex kit.

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

209 ng material, yet until recently there was no kit available enabling both.

210 hygienic waste management, ritual-feeding of kites (mainly operated by Muslims), human density, and p

211 partner HIV testing through distribution of kits within their sexual networks.

212 ex System (CODIS) yield (i.e., the number of kits that generate at least one DNA profile for the crim

213 es, suggesting differential vulnerability of kits to infection by the Zika virus or to subsequent mec

214 alyses regardless of the primer-probe set or kit used.

215 iciently reproduces the results of the other kits at the level of pathway analysis while providing a

216 f options that is not available in the other kits.

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

218 ovided with the Biocrates AbsoluteIDQ p400HR kit, to quantify up to 408 metabolites.

219 ntial gene expression; for example, the Pico kit results in 55% fewer differentially expressed genes

220 In summary we conclude that the Pico kit sufficiently reproduces the results of the other kit

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

222 mina TruSeq stranded mRNA Sample Preparation kit (TruSeq) requires abundant starting material while t

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

224 t when several commercial sample-preparation kits are used following manufacturer protocols.

225 This Q-tube gas purging kit assisted-protocol features safe due to easy pressing

226 pg/muL of DNA, similar to the available qPCR kits, is achieved, but it is cheaper, easier and avoids

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

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

229 he validation of other platforms and reagent kits.

230 By linking field data of 1,075 poisoned red kites to changes in occupancy and abundance across 274 s

231 parties using a commercially available REFtb kit to determine whether incorporation of REFtb into the

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

233 feasible with conventional emergency rescue kits.

234 Takara Bio SMART-Seq v4 Ultra Low Input RNA kit (V4) sacrifices strand specificity.

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

236 lephone genetic counseling and mailed saliva kits resulted in high testing uptake among ARRs.

237 number of surveys are mailed a saliva sample kit ("spit kit") to collect DNA for genotyping.

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

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

240 fic private alleles (e.g., due to sequencing kits, and genetic ancestries).

241 enging with no validated commercial serology kits available.

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

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

244 urveys are mailed a saliva sample kit ("spit kit") to collect DNA for genotyping.

245 ion requirements, and collected >27,000 spit kits.

246 9, we engaged >80,000 individuals, sent spit kits to >32,000 individuals who met minimum participatio

247 viability was assessed using LIVE/DEAD stain kit and the recellularised scaffolds were further assess

248 escence microscopy and the bacteria staining kit Live/Dead BacLight(TM) to quantify viable LAB popula

249 ools of up to 32 samples, using the standard kits and protocols, with an estimated false negative rat

250 kinship applications as a supplementary STR kit following the minimum criteria for validation recomm

251 ver, these are expensive, and supply of such kits in sufficient numbers cannot always be guaranteed.

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

253 The MLPA telomere kit was used to identify aneuploidy through detection of

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

255 ied using the PBP2' latex agglutination test kit (Thermo Fisher Scientific) with sensitivity and spec

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

257 during the household visit, an HIV self-test kit could be left for secondary distribution to the abse

258 there is currently a shortage of RT-PCR test kits, underscoring the urgent need for alternative metho

259 mmercially available SARS-CoV-2 RT-qPCR test kits and backfill pipeline shortages.

260 0-times sensitive than commercial rapid test kits (RIDTs).

261 results has recently been added to the test kits.

262 The kit which gave the least variable results was based on d

263 Manufacturing the kit in larger quantities could reduce the cost of the ma

264 In this study, the kit was evaluated for kinship applications as a suppleme

265 00, 500, and 1,000 ng/ml) was applied to the kit and the detection limit and assay reproducibility we

266 of peanut from unprocessed samples using the kit supplied buffers were 46 +/- 5 and 28 +/- 2 with the

267 The kits displayed a number of features compatible with an i

268 We report differences between the kits at the level of differential gene expression; for e

269 Characteristics of the kits are comprehensively evaluated.

270 pregnant until gestational day 40, when the kits were delivered by caesarian section.

271 Comparative evaluation of these kits is important for selecting the appropriate protocol

272 d random measurement errors when using these kits and suggest measures to detect and quantify them.

273 This kit has the technical characteristics to be employed as

274 We compared the three kits in a realistic differential expression analysis.

275 f biological interest with each of the three kits.

276 A commercial IgG TIIA kit was selected as a demonstrative model to characteriz

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

278 ensively understanding nature's genetic tool kit can we predict how phenotypes arise from the complex

279 ribosomal requirement with the genetic tool kit presented in Artiles et al. (2019) suggests a checkp

280 id expansion protocol and a laboratory "tool kit" for dissecting the functions of Fzd subtypes in ste

281 ive Multi-drug combinations), an online tool kit that can effectively predict drug synergy.

282 he ancestral ribosome and increases the tool kit for RNA nanotechnology and synthetic biology.

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

284 n, with available genomes and molecular tool kits.

285 years and vastly expanded neuroscience tool kits remain applicable today.

286 quirements imposed by the use of varied tool-kits.

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

288 ared with existing methods, including TRIZOL kit (Invitrogen), Plant RNeasy mini kit (Qiagen), Furtad

289 ncing of control DNA samples and compare two kits, the Illumina TruSight One and the Agilent SureSele

290 Centrifugal spin-type kits are extensively used for the desalting or buffer-ex

291 say were combined to generate a ready-to-use kit for rapid detection of porcine admixtures in process

292 ng spectrophotometry as gold standard (using kits from Trinity Biotech PLC, Wicklow, Ireland) were in

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

294 the MiSeq, assuming a 2 x 150 bp run on a v3 kit.

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

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

297 ly from unprocessed samples with the Veratox kit.

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

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

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