نتایج جستجو برای: loop mediated isothermal amplification method lamp

تعداد نتایج: 2179620  

Journal: :Forests 2021

A Loop-Mediated Isothermal Amplification (LAMP) assay was developed for the detection of pine pathogen Dothistroma septosporum (G. Dorog.) M. Morelet. The specificity LAMP tested using a selection needle fungi, including pini Hulbary, and Lecanosticta acicola (Thüm.) Syd.; only D. DNA amplified by test. In terms sensitivity, able to detect as little 1 pg total DNA. This enables extracted from d...

2010
RAMESH

A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed for detecting the E1 gene of Chikungunya virus (CHIKV). The RT-LAMP assay is a novel method of gene amplification that amplifies nucleic acid with high specificity, efficiency, and rapidity under isothermal conditions with a set of six specially designed primers that recognize eight distinct sequences o...

2016
Yee-Ling Lau Meng-Yee Lai Mun-Yik Fong Jenarun Jelip Rohela Mahmud

The lack of rapid, affordable, and accurate diagnostic tests represents the primary hurdle affecting malaria surveillance in resource- and expertise-limited areas. Loop-mediated isothermal amplification (LAMP) is a sensitive, rapid, and cheap diagnostic method. Five species-specific LAMP assays were developed based on 18S rRNA gene. Sensitivity and specificity of LAMP results were calculated as...

کرمی, علی ,

مقدمه:سالمونلاها از مهمترین باکتری های بیماری و عامل تیفوئید، باکتریمی، آنتروکولیت و سالمونلوز است که از عفونت های مشترک انسان و حیوانات می باشد. بیماریهای ناشی از این عامل یک معضل بزرگ بهداشتی در جهان به خصوص در کشورهای در حال توسعه از جمله کشور ما می باشد. بنابراین تشخیص سریع، دقیق و به موقع آن برای جلوگیری از اپیدمی و عوارض مخرب این باکتری ضروری به نظر می رسد. برای تشخیص سالمونلا روش های مخت...

Journal: :Journal of clinical microbiology 2010
Ashok Kumar Reddy Praveen Kumar Balne Rajeev Kumar Reddy Annie Mathai Inderjeet Kaur

A loop-mediated isothermal amplification (LAMP) assay for the rapid detection of cytomegalovirus (CMV) was developed and evaluated. The LAMP assay specifically amplified only CMV DNA, and no cross-reactivity with the DNA of herpes simplex virus type 1, varicella-zoster virus, adenovirus, Aspergillus flavus, or Staphylococcus aureus was observed. The sequences of the LAMP assay-positive CMV prod...

Journal: :Applied and environmental microbiology 2004
Ram Savan Arisa Igarashi Satoru Matsuoka Masahiro Sakai

Here we report a rapid and sensitive method (using loop-mediated isothermal amplification [LAMP]) for the diagnosis of edwardsiellosis, a fish disease caused by Edwardsiella tarda, in Japanese flounder. A set of four primers was designed, and conditions for the detection were optimized for the detection of E. tarda in 45 min at 65 degrees C. No amplification of the target hemolysin gene was det...

2016
Gaolian Xu Hang Zhao Jonathan M Cooper Julien Reboud

We demonstrate a multiplexed loop mediated isothermal amplification (LAMP) assay for infectious disease diagnostics, where the analytical process flow of target pathogens genomic DNA is performed manually by moving magnetic beads through a series of plugs in a capillary. Heat is provided by a water bath and the results are read by the naked eye, enabling applications in low resource settings.

Journal: :Chemical communications 2015
Gaolian Xu Rory N Gunson Jonathan M Cooper Julien Reboud

We describe a nucleic acid testing (NAT) platform for infectious disease diagnostics at the point-of-care, using surface acoustic waves (SAW) to perform a multiplexed loop-mediated isothermal amplification (LAMP) test for sexually transmitted diseases. The ultrasonic actuation not only enables faster NAT reactions but also provides a route towards integrating low-cost, low-power molecular diagn...

Journal: :Journal of microbiological methods 2013
Po-Chi Soo Chun-Chieh Tseng Siao-Ru Ling Ming-Li Liou Chih-Chin Liu Huei-Jen Chao Teng-Yi Lin Kai-Chih Chang

Here we report the design and evaluation of a loop-mediated isothermal amplification (LAMP) assay for detecting Acinetobacter baumannii DNA based on the 16S-23S rRNA intergenic spacer (ITS) sequence. The results showed that target DNA was amplified and visualized within 30min and with a detection limit 100-fold greater than PCR.

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