ライフサイエンスコーパス: LAMP

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

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

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

4 LAMP-2B regulates lysosome maturation to impact macroaut

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

6 LAMP-AuNP and LAMP-STR can detect as low as 9.7 fg (3.2

7 d by lysosome-associated membrane protein 1 (LAMP-1)-positive vesicles based on short hairpin RNA (sh

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

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

10 in lysosomal-associated membrane protein 2 (LAMP-2) gene are associated with Danon disease, which of

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

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

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

14 In this work, we developed a LAMP-based point-of-care platform for detection of bacte

15 cking to facilitate cell-to-cell spread in a LAMP-1-dependent mechanism.IMPORTANCE MDV disrupts lipid

16 This is the first report of a LAMP method for a PCV13 serotype-specific identification

17 In this study, a LAMP method is developed for facile visual detection of

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

19 iated isothermal nucleic acid amplification (LAMP) and bioluminescent assay in real time (BART), with

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

21 with loop-mediated isothermal amplification (LAMP) and a compact, portable, integrated microfluidic p

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

23 ning loop-mediated isothermal amplification (LAMP) and disposable electrochemical sensors based on sc

24 sing loop-mediated isothermal amplification (LAMP) and provides real-time, naked-eye detection with H

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

26 Loop-mediated isothermal amplification (LAMP) as a diagnostic tool is rapidly gaining recognitio

27 sing loop-mediated isothermal amplification (LAMP) as the chemistry for targeted DNA detection, by vi

28 1&2 loop-mediated isothermal amplification (LAMP) assay (Meridian Bioscience, Cincinnati OH) for the

29 tric loop-mediated isothermal amplification (LAMP) assay and smartphone-based color analysis, enablin

30 ovel loop-mediated isothermal amplification (LAMP) assay based on the sequences available for the 13

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

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

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

34 y, a loop-mediated isothermal amplification (LAMP) assay was designed for the specific detection of M

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

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

37 sing loop-mediated isothermal amplification (LAMP) combined with nanogold probe (AuNP) or styryl dye

38 hile loop-mediated isothermal amplification (LAMP) detected 2/10.

39 elop loop-mediated isothermal amplification (LAMP) diagnostic tests.

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

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

42 ital loop-mediated isothermal amplification (LAMP) for the detection and quantification of HPV DNA.

43 y of loop-mediated isothermal amplification (LAMP) for the detection of the BRAF V600E single-nucleot

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

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

46 Loop-mediated isothermal amplification (LAMP) is a powerful nucleic acid amplification technique

47 Loop-mediated isothermal amplification (LAMP) is a prevailing nucleic acid isothermal amplificat

48 Loop-mediated isothermal amplification (LAMP) is increasingly used in molecular diagnostics as a

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

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

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

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

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

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

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

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

57 n of loop-mediated isothermal amplification (LAMP) targeting the waterborne pathogen Vibrio cholerae

58 e of loop-mediated isothermal amplification (LAMP) to detect PIK3CA c.3140 A > G (H1047R), a prevalen

59 ital loop-mediated isothermal amplification (LAMP) using commercially available microfluidic chips an

60 Loop-mediated isothermal amplification (LAMP) was compared to traditional rapid diagnostic testi

61 CR)/ loop mediated isothermal amplification (LAMP) was observed using the MTAT strategy (odds ratio [

62 (RT) loop-mediated isothermal amplification (LAMP) with clustered regularly interspaced short palindr

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

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

65 nts, loop-mediated isothermal amplification (LAMP), an extremely sensitive nucleic acid test, specifi

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

67 lood loop-mediated isothermal amplification (LAMP), and placental histopathology.

68 T]), loop-mediated isothermal amplification (LAMP), and quantitative reverse transcription polymerase

69 CR), loop-mediated isothermal amplification (LAMP), and reverse transcription (RT).

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

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

72 h as loop-mediated isothermal amplification (LAMP), show great utility for the development of rapid d

73 with loop-mediated isothermal amplification (LAMP), the CHB probe could detect Borrelia burgdorferi (

74 n of loop mediated isothermal amplification (LAMP).

75 cs for use with loop-mediated amplification (LAMP) as a bridge between concentrated and dilute templa

76 Loop-mediated amplification (LAMP) is a nucleic acid amplification method that has be

77 They are positive for EEA-1 and LAMP-1 and contain watery fluid but not organelles.

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

79 LAMP-AuNP and LAMP-STR can detect as low as 9.7 fg (3.2 sea copies) an

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

81 that MDV gB colocalizes with cholesterol and LAMP-1, suggesting that viral protein trafficking is med

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

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

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

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

86 and disintegration, and enlarged and annular LAMP-1-positive organelles in AMD RPE.

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

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

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

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

91 Here, we identify the LAMP-2 isoform B (LAMP-2B) as required for autophagosome-lysosome fusion i

92 thus mainly focus on the paper device-based LAMP assay for the rapid infectious disease diagnosis, f

93 Both LAMP amplicons were simultaneously hybridized with ssDNA

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

95 Both LAMP tests possess remarkable species-specificity as the

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

97 hat viral protein trafficking is mediated by LAMP-1-positive vesicles in association with cholesterol

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

99 This phenotype was recapitulated by LAMP-2B knockout in non-Danon hiPSC-CMs.

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

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

102 Also, this CHB-enhanced LAMP (CHB-LAMP) assay was successfully demonstrated to detect B. b

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

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

105 rter detection time compared to conventional LAMP and PCR methods.

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

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

108 However, the current LAMP methods, especially LAMP with two loop primers, suf

109 ound pork and 10 CFU/mL in milk in 5-7 days, LAMP-AuNP could detect down to 10 CFU/g for both samples

110 ssociated membrane protein 3 (LAMP3/CD208/DC-LAMP) in a subset of Sjogren's syndrome cases.

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

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

113 nts and a foundation for targeting defective LAMP-2B-mediated autophagy to treat this patient populat

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

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

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

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

118 uidic chip was designed to carry out digital LAMP.

119 l the necessary workflows to perform digital LAMP using standard laboratory equipment and commerciall

120 As a proof of concept, we performed digital LAMP on a sp-SlipChip to quantify human papillomaviruses

121 We validated this digital LAMP assay and pipeline by performing a phenotypic antib

122 We then develop a real-time digital LAMP (dLAMP) with high-resolution melting temperature (H

123 t of contact angle from oil-immersed droplet LAMP reactions.

124 Monitoring of droplet LAMP reactions was demonstrated in a three-compartment,

125 Smartphone-captured images of droplet LAMP reactions, and their contact angles, were evaluated

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

127 Also, this CHB-enhanced LAMP (CHB-LAMP) assay was successfully demonstrated to d

128 owever, the current LAMP methods, especially LAMP with two loop primers, suffer from undesired nonspe

129 and compared the results between established LAMP and conventional PCR assays.

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

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

132 Here, we have developed the first LAMP assay for mcr-9 - showing high sensitivity (down to

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

134 These ultra-quantification methods for LAMP amplification either singularly or in combination h

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

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

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

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

139 Ps and facilitates the development of future LAMP assays for a wide-range of targets.

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

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

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

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

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

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

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

147 ticular primers will help inform and improve LAMP primer design.

148 o specific and non-specific amplification in LAMP that are difficult to deduce from bulk measurements

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

150 This work expands the use of MBs in LAMP for the visual detection of SNPs and facilitates th

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

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

153 approach by testing variables that influence LAMP reaction speed and the probability of detection.

154 Instead, LAMP-2B interacts with autophagy related 14 (ATG14) and

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

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

157 e virion-containing MCs emerged from larger, LAMP-1-positive membranous organelles that are morpholog

158 in addition to low-cost and robustness, make LAMP an attractive alternative to polymerase chain react

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

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

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

162 icroscopy in detecting asymptomatic malaria, LAMP is superior still.

163 accumulate the late endosome/lysosome marker LAMP-1 during macrophage infection.

164 The performed work expands the use of MB-LAMP for SNP detection as well as demonstrates SPME as a

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

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

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

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

169 Microfluidic LAMP-BART droplets with high stability and uniformity of

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

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

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

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

174 NA) gene silencing and the colocalization of LAMP-1, glycoprotein B (gB) of MDV, and cholesterol (fil

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

176 Finally, gene correction of LAMP-2 mutation rescues the Danon phenotype.

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

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

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

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

181 sis for this is that real-time monitoring of LAMP reactions either by bioluminescent reporting (BART)

182 ains a key challenge for the optimization of LAMP assays.

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

184 ion substantially reduced the reliability of LAMP and limited its applications in clinical diagnostic

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

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

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

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

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

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

191 There is an overwhelming variety of LAMP indicators in the literature, yet a comprehensive c

192 namic range quantification strategy based on LAMP, in a closed tube, undiluted sample molecular diagn

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

194 ection of malaria parasites by microscopy or LAMP was not associated with adverse birth outcomes.

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

196 Furthermore, our LAMP-AuNP detect sea at a range below the food safety co

197 Compared to reference qRT-PCR, LAMP had the highest sensitivity (92.6%, 95% confidence

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

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

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

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

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

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

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

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

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

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

208 in performance and reproducibility of qPCR, LAMP, and RT reactions.

209 Compared to RDT, LAMP provided a 3-fold and 2.3-fold higher yield to dete

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

211 oster for loop mediated isothermal reaction (LAMP).

212 Remarkably, LAMP-2B functions independently of syntaxin 17 (STX17),

213 RT-LAMP of crude samples had substantially lower sensitivit

214 RT-LAMP of RNA purified from COVID-19 patient samples had p

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

216 n loop-mediated isothermal amplification (RT-LAMP) assay compatible with current reagents, which util

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

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

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

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

221 n loop-mediated isothermal amplification (RT-LAMP) to diagnose coronaviruses.

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

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

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

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

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

227 T-loop-mediated isothermal amplification (RT-LAMP).

228 n loop mediated isothermal amplification (RT-LAMP).

229 Here, we report an RT-LAMP isothermal assay for the detection of severe acute

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

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

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

233 Diagnostic performances by CRISPR and RT-LAMP on purified RNA were similar.

234 samples using RT-qPCR, CRISPR-Cas13a, and RT-LAMP.

235 After a half-hour RT-LAMP amplification, the tube was inverted and flicked to

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

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

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

239 the exponential amplification ability of RT-LAMP and the sequence-specific processing by the CRISPR-

240 mplification efficiency or sensitivity of RT-LAMP.

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

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

243 mpling a volume of the VTM to perform the RT-LAMP assay without an RNA extraction kit.

244 purification protocol, combined with the RT-LAMP assay, brings the sensitivity to at least 1 viral R

245 This protocol, combined with the RT-LAMP assay, has a sensitivity of at least 50 viral RNA c

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

247 The RT-LAMP reagents were added to the sample vial, while CRISP

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

249 Abbott ID Now performance was similar to RT-LAMP of crude samples.

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

251 mal amplification of SARS-CoV-2 RNA using RT-LAMP, the modified crRNAs are incorporated in a paper-ba

252 reaction speed for RNA amplification via RT-LAMP.

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

254 In conclusion, a rapid and simple LAMP-based pneumococcal serotyping method has been devel

255 Moreover this highly specific LAMP detection technique can reduce the incidence of fal

256 re dramatically increased after a successful LAMP reaction.

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

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

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

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

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

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

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

264 The LAMP amplicons can be effectively detected using unmodif

265 The LAMP reactions using primers targeting V. parahaemolytic

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

267 The LAMP-STR quantitated sea in 10-1,000 CFU (7.2-720 copies

268 e numerous reported techniques to detect the LAMP amplification including turbidity, bioluminescence

269 Here, we identify the LAMP-2 isoform B (LAMP-2B) as required for autophagosome

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

271 For validating the translation of the LAMP assay onto a LoC platform, a subset of the samples

272 We confirmed the specificity of the LAMP assay using 41 serotypes of pneumococcal strains.

273 The sensitivity of the LAMP assay was 10 to 100 copies per reaction, compared t

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

275 The detection limits of the LAMP assay were comparable when using DNA-spiked CSF and

276 ts clinical use, the detection limits of the LAMP assay were evaluated using bacterial genomic DNA-sp

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

278 nd is therefore a fundamental feature of the LAMP initiation event.

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

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

281 g 80 pork and milk samples revealed that the LAMP-AuNP showed 100% sensitivity, 97-100% specificity a

282 een replicates at low copy number due to the LAMP amplification mechanism.

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 ther African MSV isolates indicate that this LAMP assay can be used for detecting MSV in maize sample

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

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

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

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

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

291 Stable, uniform LAMP-BART droplets are generated with low cost equipment

292 that quenched fluorescent labels on various LAMP primers can be used to quantify and detect target D

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

294 Our crude DNA lysis combined with LAMP-AuNP/STR present effective point-of-care detection

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

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

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

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.