ライフサイエンスコーパス: LAMP

1 LAMP and qPCR exhibited similar analytical sensitivities

2 LAMP dramatically lowers the detection threshold achieva

3 LAMP is one of the most promising point-of-care (POC) ge

4 LAMP primers were designed to target a conserved gene en

5 LAMP-2A is a transmembrane protein component for protein

6 LAMP-2A is required for chaperone-mediated autophagy (CM

7 LAMP-2B regulates lysosome maturation to impact macroaut

8 LAMP-2C levels modulated the steady-state expression of

9 ociated with lysosomal-associated protein-1 (LAMP/gag) is a potential therapeutic vaccine against HIV

10 sosome associated membrane protein (LAMP)-1, LAMP-2 and the a2 isoform of V-ATPase (a2V, an enzyme in

11 cation using the lysosomal marker protein 2 (LAMP-2) immunolabeling showed higher neuronal lysosomal

12 Lysosomal membrane protein 2 (LAMP-2) is a target of antineutrophil cytoplasmic autoan

13 the lysosome-associated membrane protein-2 (LAMP-2) regulate these pathways influencing immune recog

14 ysosome-associated membrane protein type 2a (LAMP-2A) together with a complex of chaperones and co-ch

15 This interval is sufficient to allow a LAMP reaction for the Escherichia coli malB gene to proc

16 amplified fields (hot spots) in and around a LAMP are at the expense of other regions with depleted f

17 Yet, far less is known about LAMP-2C function.

18 ntion, presence of Rab5B, failure to acquire LAMP-1 and inability to acidify.

19 The HPV-58 detection was compared among LAMP-QCM, conventional LAMP and nested PCR in 50 cervica

20 via loop mediated isothermal amplification (LAMP) allowing for quantitative analysis of the cMYC pro

21 ning loop-mediated isothermal amplification (LAMP) and AC susceptometry, we demonstrate a rapid and h

22 ered loop-mediated isothermal amplification (LAMP) and real-time electrochemical detection based on t

23 ion: Loop-mediated isothermal amplification (LAMP) and Rolling Circle Amplification (RCA) techniques

24 of a loop-mediated isothermal amplification (LAMP) assay (illumigene assay) for the diagnosis of GAS

25 1&2 loop-mediated isothermal amplification (LAMP) assay (Meridian Bioscience, Cincinnati OH) for the

26 A loop-mediated isothermal amplification (LAMP) assay for open reading frame 1 (ORF1) of the gluta

27 of a loop-mediated isothermal amplification (LAMP) assay for rapid detection of CaPVs.

28 y, a loop-mediated isothermal amplification (LAMP) assay provided rapid detection of SbGP/MPV phytopl

29 ed a loop-mediated isothermal amplification (LAMP) assay that enables rapid, low-cost detection of M.

30 of a loop-mediated isothermal amplification (LAMP) assay to facilitate rapid inexpensive molecular di

31 the Loop-Mediated Isothermal Amplification (LAMP) assay.

32 sign loop-mediated isothermal amplification (LAMP) assays for the rapid, specific, sensitive, and qua

33 tric loop-mediated isothermal amplification (LAMP) assays targeting the L. loa-specific gene sequence

34 for loop-mediated isothermal amplification (LAMP) assays were identified from draft genomes of Calon

35 with loop mediated isothermal amplification (LAMP) for monoplex pathogen detection.

36 with loop-mediated isothermal amplification (LAMP) for multiplexed instrument-free diagnosis of these

37 with loop-mediated isothermal amplification (LAMP) for the rapid, sensitive, and instrument-free dete

38 Loop-mediated isothermal amplification (LAMP) has previously been shown to be fast and effective

39 Loop-mediated isothermal amplification (LAMP) is a DNA amplification approach characterized by h

40 Loop-mediated isothermal amplification (LAMP) is limited by the accumulation of non-specific pro

41 sing loop-mediated isothermal amplification (LAMP) method and subsequently added to luminol solution

42 Loop-mediated isothermal amplification (LAMP) of DNA is a powerful isothermal nucleic acid ampli

43 the loop-mediated isothermal amplification (LAMP) of nucleic acid biomarkers and shows for the first

44 les, loop-mediated isothermal amplification (LAMP) of nucleic acids, and visual readout of assays.

45 the loop-mediated isothermal amplification (LAMP) reaction which results in improved performance.

46 of a loop-mediated isothermal amplification (LAMP) reaction with an initial number of DNA strands as

47 izes loop-mediated isothermal amplification (LAMP) reagents predeposited into distinct lanes of the m

48 A loop-mediated isothermal amplification (LAMP) system, the illumigene Mycoplasma DNA amplificatio

49 ined loop-mediated isothermal amplification (LAMP) technique with QCM, called as LAMP-QCM, for detect

50 n by loop-mediated isothermal amplification (LAMP) to amplify specifically the E. coli Tuf gene after

51 d on loop-mediated isothermal amplification (LAMP) was assessed for field use.

52 ming Loop-mediated isothermal amplification (LAMP) was developed for the detection and quantification

53 free loop mediated isothermal amplification (LAMP) was monitored in real-time with a point of use dev

54 ines loop-mediated isothermal amplification (LAMP) with a portable tube scanner real-time isothermal

55 rate loop-mediated isothermal amplification (LAMP) with ECL technique for DNA detection and quantific

56 and loop-mediated isothermal amplification (LAMP) with end point detection using a hand-held UV sour

57 ion, loop-mediated isothermal amplification (LAMP), and array-based fluorescence detection.

58 the loop mediated isothermal amplification (LAMP), are well suited for field use as they do not requ

59 ined loop-mediated isothermal amplification (LAMP), programmable toehold-mediated strand-exchange sig

60 n of loop mediated isothermal amplification (LAMP).

61 and loop-mediated isothermal amplification (LAMP).

62 cally simulates Loop-mediated AMPlification (LAMP) allowing users to efficiently test putative LAMP p

63 curacy of a new loop-mediated amplification (LAMP) kit in febrile returned travelers.

64 tors DC-LAMP and CD68, as well as LAMP-1 and LAMP-2.

65 the T4-bacteriophage-modified biosensor and LAMP can achieve screening, viability, and confirmation

66 n this study we identify LAMP-1 (CD107a) and LAMP-2 (CD107b) on the surface of human monocyte-derived

67 rison with two competing methods, HAPMIX and LAMP.

68 0 min were achieved for the impedimetric and LAMP method, respectively.

69 exhibited a striking accumulation of LC3 and LAMP-1 positive autolysosomes containing undigested cyto

70 of LAMP-SPR sensing was 10 copies/microl and LAMP-SPR sensing system showed a good selectivity toward

71 tion in LEs similar to that seen in NPC- and LAMP-deficient cells, we show that the restriction of pa

72 relationships between STEC cell numbers and LAMP turbidity signals.

73 gometry and FACS analysis for P-selectin and LAMP-1 exposure.

74 port a mechanistic relationship between anti-LAMP-2 antibodies and ANCA glomerulonephritis.

75 We measured anti-LAMP-2 reactivity in 680 sera samples (two academic cent

76 The prevalence of anti-LAMP-2 antibodies and their relationship to disease in A

77 e 1500-fold and 10,000-fold higher than anti-LAMP-2 titers, respectively.

78 However, in contrast to anti-LAMP-2 antibodies from ANCA-positive patients, these ant

79 ermore, Wistar Kyoto rats injected with anti-LAMP-2 antibodies did not develop glomerulonephritis.

80 ication (LAMP) technique with QCM, called as LAMP-QCM, for detection of high-risk human papillomaviru

81 cytic receptors DC-LAMP and CD68, as well as LAMP-1 and LAMP-2.

82 oop-mediated isothermal amplification assay (LAMP) for detection of HBV genotypes A, B, C, D, E, and

83 etection requirement, either in real-time at LAMP running temperature (~60 degrees C), or at end-poin

84 gDNA] and/or 5 mf/ml) than the LLMF342-based LAMP assay (10 pg/ml of gDNA and/or 50 mf/ml), and its a

85 The LLMF72-based LAMP assay showed greater analytic sensitivity (limit of

86 For LAMP detection, a SPR based LAMP sensing system (SPRLAMP) was constructed, including

87 l detection based on the interaction between LAMP amplicon and the redox-reactive osmium complex.

88 coated QCM surface and specific biotinylated LAMP products.

89 Both LAMP amplicons were simultaneously hybridized with ssDNA

90 Both LAMP assays were highly specific (100%) for L. loa infec

91 h 3-well nested PCR, the sensitivity of both LAMP and single-well nested PCR was 90%; the microscopy

92 immediate reporting of half of all TPs, but LAMP or CCNA was required to confirm the presence or abs

93 ogenous and membrane Ags was not affected by LAMP-2C expression in B cells.

94 s and targeting to the lysosomal membrane by LAMP-2A are coupled.

95 mal proteases activities were unperturbed by LAMP-2C ectopic expression.

96 l killer (NK) cells and deficiency of CD107a/LAMP-1 in mice resulted in increased NK cell apoptosis u

97 Importantly, knockdown of CD107a/LAMP-1 in primary human natural killer (NK) cells and de

98 hus, our data support a novel role of CD107a/LAMP-1 in the protection of NK cells from degranulation-

99 Moreover, surface expression of CD107a/LAMP-1 reduced binding of perforin to cells.

100 Intracellular expression of CD107a/LAMP-1, and to a lesser extent that of CD107b/LAMP-2, co

101 Engineered surface expression of CD107a/LAMP-1, but not of CD107b/LAMP-2, reduced the granule-me

102 was dependent on glycosylation of the CD107a/LAMP-1 hinge.

103 AMP-1, and to a lesser extent that of CD107b/LAMP-2, correlated with lymphocyte CG content.

104 pression of CD107a/LAMP-1, but not of CD107b/LAMP-2, reduced the granule-mediated killing of transfec

105 Similarly, changes in B cell LAMP-2C expression did not impact macroautophagy.

106 mplification capacities of TPrA and combines LAMP with inherently high sensitivity of the ECL techniq

107 This commercial LAMP assay is a useful rapid method for detecting M. pne

108 comparable to those obtained by conventional LAMP or qPCR approaches.

109 ared to 1000 copies detected by conventional LAMP.

110 AMP-QCM was higher than that of conventional LAMP with 100% sensitivity and 90.5% specificity.

111 on was compared among LAMP-QCM, conventional LAMP and nested PCR in 50 cervical cancer tissues.

112 ults of adding swarm primers to conventional LAMP reactions include increased amplification speed, in

113 adding a new set of primers to conventional LAMP reactions.

114 mit up to ten times compared to conventional LAMP with less-time consuming.

115 Densities of tumor HEVs and DC-LAMP(+) DCs were strongly reduced during breast cancer p

116 with the presence of gene products LAMP3/DC-LAMP and CD83, which typify mature dendritic cells (DCs)

117 toplasm reactivity in a large fraction of DC-LAMP(+) cells, instead of the classical dot-like stain.

118 breast tumor samples, and the density of DC-LAMP(+) DCs clusters was strongly correlated with the de

119 ssociated membrane glycoprotein positive (DC-LAMP+)) DCs, but with marked decreases in expression of

120 es the dendritic cell endocytic receptors DC-LAMP and CD68, as well as LAMP-1 and LAMP-2.

121 ies of HEVs (HEV(high)) and correlated to DC-LAMP, a marker of mature DCs.

122 e as shown by minimal colocalization with DC-LAMP, and coexpressed inflammatory markers tumor necrosi

123 a pool of candidate markers, we demonstrate LAMP assay specificity by testing related fungal species

124 hm-based strategy is then employed to design LAMPs that selectively enhance the response of analyte m

125 main lamellar morphology, which we designate LAMP Transmission electron microscopy indicates that LAM

126 Furthermore, we detected LAMP-2 autoantibodies in two ANCA-negative patients.

127 sothermal amplification (qLAMP), and digital LAMP (dLAMP), for the detection and quantification of hu

128 ophilic PDMS surfaces that allow for digital LAMP to be performed in a self-driven microfluidic devic

129 In "digital LAMP", small quantities of both template DNA and reagent

130 uidic chip was designed to carry out digital LAMP.

131 -loop-mediated isothermal amplification (dRT-LAMP) for quantification of HIV viral RNA.

132 count and the expected concentration) of dRT-LAMP 10-fold, from approximately 2% to approximately 23%

133 We showed here that when one-step dRT-LAMP is used for quantification of HIV RNA, the digital

134 gital format that counts molecules using dRT-LAMP chemistry detected a 2-fold change in concentration

135 Consequently, deletion of the gene encoding LAMP-2A in T cells caused deficient in vivo responses to

136 more, B. neotomae exhibited early endosomal (LAMP-1) and late endoplasmic reticulum (calreticulin)-as

137 To examine LAMP-2C function in human B cells and specifically its r

138 will likely benefit most if not all existing LAMP assays based on state-of-the-art, six-primer reacti

139 For LAMP detection, a SPR based LAMP sensing system (SPRLAMP

140 on of paper into the microfluidic device for LAMP reactions enables stable test results over a much l

141 Primers for LAMP were designed to amplify the Hcp100 locus of H. cap

142 antees a significant and reliable signal for LAMP reaction amplified from as little as 10(-19) M viru

143 owever, common detection techniques used for LAMP and RT-LAMP have drawbacks, including poor discrimi

144 Finally, IgG from LAMP-2-positive ANCA-negative patients bound specificall

145 identified two VEGF-C/NRP-2-regulated genes, LAMP-2 and WDFY-1, that have previously been suggested t

146 r local ancestry inference software: HAPMIX, LAMP, LAMP-LD, and ELAI.

147 These results demonstrate that our HBV-LAMP assay is rapid, sensitive and specific, and capable

148 We have shown that the Hcp100 LAMP assay is a rapid affordable assay that can be used

149 The Hcp100 LAMP assay was 100% sensitive and specific when tested w

150 and isothermal amplification (e.g. RPA, HDA, LAMP, NASBA, RCA, ICAN, SMART, SDA).

151 focus on the detection of purified DNA here, LAMP has previously been demonstrated with a range of cl

152 ynamics of the transmembrane domain of human LAMP-2A in n-dodecylphosphocholine micelles by nuclear m

153 c loop-mediated isothermal amplification (iD-LAMP) and quantitative optical read-out by a disc drive.

154 In this study we identify LAMP-1 (CD107a) and LAMP-2 (CD107b) on the surface of hu

155 In summary, we identify LAMP-2 as an endocytic receptor on human MoDC that route

156 n CpG-B and induces DNase II localization in LAMP-2(+) lysosomes.

157 e alternating metal and dielectric shells in LAMPs are designed such that, when illuminated, the plas

158 howed increased lysosomal proteins including LAMP-2, cathepsin D and LC3.

159 Increased LAMP-2C expression in B cells did not alter MHCII expres

160 The integrated LAMP-QCM system has improved the detection limit up to t

161 PLEKHM2 joins LAMP-2 and BAG3 as a disease gene altering autophagy res

162 l ancestry inference software: HAPMIX, LAMP, LAMP-LD, and ELAI.

163 In summary, LLMF72 LAMP represents a new molecular diagnostic tool that is

164 Malaria LAMP (Eiken Chemical, Japan) was evaluated for samples f

165 Malaria LAMP had a diagnostic accuracy similar to that of nested

166 Malaria LAMP in a remote Ugandan clinic achieved sensitivity sim

167 The performance of a commercial malaria LAMP assay (Illumigene Malaria LAMP) was evaluated using

168 The Illumigene Malaria LAMP assay was easily implemented in the clinical labora

169 rcial malaria LAMP assay (Illumigene Malaria LAMP) was evaluated using two sample preparation workflo

170 Microscopy was performed, and then malaria LAMP was performed using Plasmodium genus and Plasmodium

171 The late endosomal/lysosomal marker LAMP-1 accumulated around the parasite in CD40-stimulate

172 tially colocalized with the lysosomal marker LAMP-1.

173 colocalizes with mature phagolysosome marker LAMP-1 and with vacuolar proton ATPase in macrophages.

174 Meningococcal LAMP is straightforward enough for use in any hospital w

175 ess the diagnostic accuracy of meningococcal LAMP as a near-patient test in the emergency department.

176 s and tested with near-patient meningococcal LAMP and the results were compared with those obtained b

177 lations using Linkage Disequilibrium method (LAMP-LD) and evaluated the association with common carot

178 iparum qPCR titer of >/= 2 parasites/microL, LAMP sensitivity was 97.8% (95% confidence interval, 93.

179 me detection of different genes in multiplex LAMP reactions also proved possible.

180 tibodies from all 8 patients bound to native LAMP-2 purified from human glomeruli and recombinant hLA

181 Most false-negative LAMP results involved samples with parasitemia levels de

182 matrices such as human blood, using a novel LAMP primer set for bacteriophage MS2 (a model RNA virus

183 Accumulation of LAMP-1 and killing of T. gondii were dependent on the au

184 om M. smegmatis decreases the association of LAMP-3 with bead phagosomes, indicating that P27 itself

185 the formation of the higher order complex of LAMP-2A required for translocation.

186 s on the sensor surface for the detection of LAMP amplicons from MRSA.

187 owerful, real-time and specific detection of LAMP products remains analytically challenging.

188 enomics-based approach to the development of LAMP diagnostic assays is the first of its kind for fung

189 epant results resolved 4 results in favor of LAMP, suggesting that the primary analysis had underesti

190 The detection limit of LAMP-SPR sensing was 10 copies/microl and LAMP-SPR sensi

191 To achieve acceptable performance of LAMP at the microscopy center level, significant trainin

192 The performance of LAMP was compared to that of a highly sensitive quantita

193 Prevalence of LAMP-2 autoantibodies was similar in both those with mye

194 The positive rate of LAMP-QCM was higher than that of conventional LAMP with

195 Restoration of LAMP-2A in T cells from old mice resulted in enhancement

196 In order to both improve the specificity of LAMP detection and to make readout simpler and more reli

197 accuracy were sensitivity and specificity of LAMP results, compared with those of nested PCR.

198 This cytosolic tail of LAMP-2A interacts with chaperone Hsc70 and a CMA substra

199 To further facilitate the use of LAMP assays in remote settings, simpler sample preparati

200 The use of LAMP eliminates the need for the cycling of temperatures

201 respiratory and blood specimens with use of LAMP was accurate (sensitivity 89% [95% CI 72-96], speci

202 These results indicate that the use of LAMP/gag-DC may be an efficient strategy for enhancing i

203 derived dendritic cells (MoDC) and show only LAMP-2 is internalized after ligation by specific Abs, i

204 EEA-1-positive (EEA-1(+)) early endosomes or LAMP-1(+) late endosomes/lysosomes.

205 n of Col-I with LC3, an autophagy marker, or LAMP-1, a lysosome marker, whereas treatment with TFP, a

206 e to amplification processes, such as PCR or LAMP.

207 limits of detection of a few DNA copies per LAMP zone for N. meningitidis, S. pneumoniae and Hib wer

208 ion of N. meningitidis is about 3 copies per LAMP zone within 45 min, close to single-bacterium detec

209 The liquid-phase LAMP-QCM prototype comprised the frequency counter, a te

210 -mediated isothermal amplification platform (LAMP) may change this.

211 tions in a simple, inexpensive and portable "LAMP box" supplemented with a consumer class smartphone.

212 AMPs, suggesting that Pompe iPSC-CMs produce LAMPs lacking appropriate glycosylation.

213 associated to lysosomal associated protein (LAMP) sequence (LAMP/gag vaccine).

214 Lysosome-associated membrane protein (LAMP) 1/CD107a is used as a marker for NK-cell degranula

215 or the lysosome-associated membrane protein (LAMP) and by pharmacological inhibition of phagosome aci

216 The lysosome-associated membrane protein (LAMP) family includes the dendritic cell endocytic recep

217 and DC-lysosome-associated membrane protein (LAMP), low levels of MIP1-beta/CCL4, MIG/CXCL9, and seve

218 ent of lysosome associated membrane protein (LAMP)-1, LAMP-2 and the a2 isoform of V-ATPase (a2V, an

219 e.g., lysosomal-associated membrane protein [LAMP-1]) with lysosomes.

220 ellular Salmonella recruit the host proteins LAMP-2A and Hsc73, key components of the host protein tu

221 d the lysosome-associated membrane proteins (LAMP) 1 and 2 are important for robust liver-stage P. be

222 the lysosomal-associated membrane proteins (LAMPs) appear on the cell surface after CG exocytosis, w

223 allowing users to efficiently test putative LAMP primers on a set of target sequences.

224 iated isothermal DNA amplification reaction (LAMP) targeting a pathogenic bacteria gene, showing bene

225 oster for loop mediated isothermal reaction (LAMP).

226 ession of the CMA-related lysosomal receptor LAMP-2A.

227 RT-LAMP reactions were performed on a battery-operated isot

228 n-loop-mediated isothermal amplification (RT-LAMP) and the ESEQuant tube scanner, a portable isotherm

229 loop-mediated, isothermal amplification (RT-LAMP) assay for rapid detection of ZIKV and its implemen

230 n-loop-mediated isothermal amplification (RT-LAMP) assay, quantitative RT-PCR (qRT-PCR), and IgM- and

231 n-loop-mediated isothermal amplification (RT-LAMP) has frequently been proposed as an enabling techno

232 e loop-mediated isothermal amplification (RT-LAMP) of the glycoprotein gene of EBOV.

233 n loop-mediated isothermal amplification (RT-LAMP) was used subsequently to amplify the viral RNA.

234 n loop-mediated isothermal amplification (RT-LAMP) with our recently developed quenching of unincorpo

235 e loop-mediated isothermal amplification (RT-LAMP) with SYTO-9 as the signal reporter.

236 transcription, exponential amplification (RT-LAMP), and linear degradation (restriction enzymes) star

237 e loop-mediated isothermal amplification (RT-LAMP), demonstrating that the plasma is sufficiently pur

238 ranscription loop-mediated amplification (RT-LAMP).

239 ranscription loop-mediated amplification, RT-LAMP) in the context of fluctuations in temperature and

240 mbination with ELISA, both the RT-RPA and RT-LAMP assays increased the detection of acute DENV infect

241 one already found for RT-PCR, NASBA, and RT-LAMP assays.

242 on detection techniques used for LAMP and RT-LAMP have drawbacks, including poor discrimination capab

243 ction limit of the newly developed immuno-RT-LAMP assay was as low as 1.62x10(1) 50% embryo infectiou

244 Our results indicate that immuno-RT-LAMP is a novel, effective point-of-care virus identific

245 mediated isothermal amplification (immuno-RT-LAMP) assay for the rapid detection of AIV H5N1 in whole

246 mplification efficiency or sensitivity of RT-LAMP.

247 Positive RT-LAMP reactions resulted in the precipitation of magnesiu

248 concordance (kappa of >/=0.723) with the RT-LAMP and qRT-PCR assays in detecting the dengue viremic

249 into the microfluidic chip to detect the RT-LAMP reaction product directly on the chip itself by mea

250 Limit of detection of this RT-LAMP assay was 2.8 x 10(2) plaque-forming units (PFU)/te

251 N1 gene was exponentially amplified using RT-LAMP on either a real-time PCR instrument for quantitati

252 reaction speed for RNA amplification via RT-LAMP.

253 ysosomal associated protein (LAMP) sequence (LAMP/gag vaccine).

254 For each species, LAMP contains interactive diagrams of each pathway, hype

255 re dramatically increased after a successful LAMP reaction.

256 The target LAMP DNA bound electrostatically with [Ru(bpy)3](+2) on

257 Overall, TB-LAMP sensitivities among culture-positive samples were 9

258 eru to establish the feasibility of using TB-LAMP (Eiken Chemical Co.) in microscopy laboratories com

259 nsmission electron microscopy indicates that LAMP exhibits ACBC domain connectivity, in contrast to c

260 nforces these observations and predicts that LAMP is thermodynamically stable below a critical chiAC,

261 We showed that LAMP-2A exists as a homotrimer in which the membrane-spa

262 r LAMP2 and NPC1 protein levels suggest that LAMP proteins represent a significant cholesterol bindin

263 The LAMP assay detected HBV genotypes A-F and demonstrated a

264 The LAMP assay detected Hcp100 in 67% of antigen-positive ur

265 The LAMP assay was as sensitive as the PCR assay while being

266 The LAMP-ECL sensor is shown to be highly specific, sensitiv

267 F72-based qPCR and time to positivity by the LAMP assay, and performance measures of sensitivity, spe

268 In conclusion, the LAMP assays developed in this study may facilitate rapid

269 In conclusion, the LAMP reaction could be detected with the SPRLAMP sensing

270 and 10 to 20 CFU/25 g) of STEC cultures, the LAMP assays achieved accurate detection after 6 to 8 h e

271 cific primers specifically developed for the LAMP method in detecting P. vivax.

272 were 98.4% and 98.1%, respectively, for the LAMP P. falciparum primers and 97.0% and 99.2%, respecti

273 of the four loop products amplified from the LAMP is transduced to an active catalyst ssDNA which can

274 website has been completely rewritten in the LAMP (Linux, Apache, MySQL and PHP) environment.

275 (9) cfu/mL, while the linear response of the LAMP approach was determined to be 10(2)-10(7) cfu/mL.

276 The sensitivity of the LAMP assay was 88.5% tested on extracted nucleic acid an

277 ed for the development and validation of the LAMP assay.

278 utive loading, mixing, and aliquoting of the LAMP primers/reagents and DNA sample solutions were acco

279 Then, the amplicons of the LAMP reaction were detected using the calcein colorimetr

280 In the second step, we perform the LAMP amplification on all individual DNA molecules in pa

281 Since the LAMP and electrochemical analysis are implemented within

282 By simply varying the run time, the LAMP assay was able to accurately distinguish individual

283 oven histoplasmosis were evaluated using the LAMP assay.

284 reproduced the higher mobility forms of the LAMPs, suggesting that Pompe iPSC-CMs produce LAMPs lack

285 Thus, LAMP-2C serves as a natural inhibitor of CMA that can se

286 causing bacterium, Borrelia burgdorferi, to LAMP-1 lysosomal compartments.

287 ) -alkylguanine-DNA alkyltransferase) led to LAMP-to-hCG signal transduction on low-cost, commerciall

288 epidermal growth factor (EGF) trafficking to LAMP-2-positive compartments and EGF receptor degradatio

289 y gave positive responses in presence of two LAMP loops.

290 sputum and blood hemoculture were undergone LAMP amplification for 0.18 kbp and 0.23 kbp DNA fragmen

291 between genotypes and TOF was assessed using LAMP.A rare SNP (c.807C > T; rs56085230) discovered by s

292 tor 1 enhanced bacterial colocalisation with LAMP-1 and reduced their intracellular survival.

293 erve fibers but was found to colocalize with LAMP-1 and cathepsin D during early stages of axonal spr

294 CpG-A shows higher co-localization with LAMP-2(+) lysosomes than CpG-B and induces DNase II loca

295 ticles (streptavidin-MNPs) are premixed with LAMP reagents including the analyte and biotinylated pri

296 full integration of sample preparation with LAMP amplification and end point detection with a limit

297 In conclusion, antibodies that react with LAMP-2 may exist at very low titers in a minority of pat

298 Human DCs transfected with LAMP/gag (Lg-hDCs) were also activated and able to stimu

299 tion of mice with mouse DCs transfected with LAMP/gag (Lg-mDCs) stimulated more potent B- and T-cell

300 treatment only, IL-1beta was detected within LAMP-1-positive multivesicular bodies.