نتایج جستجو برای: rolling circle amplification rca

تعداد نتایج: 101614  

2015
Megha Biradar

In this thesis, we tried to improve the initiation of Rolling Circle Amplification (RCA) on genomic DNA using an approach known as Single Primer Extension (SPE). Usually, a synthetic DNA target provides a high signal on RCA after padlock probe hybridisation due to its short 3’ end. However, unfragmented genomic DNA provides low efficiency for RCA initiation due to its long 3’ end. During SPE, t...

Journal: :BioTechniques 2018
Beibei Zhang Qiao Wang Jian Wu Yin Chen Jinke Wang

This paper presents a new rolling circle amplification (RCA) technique using stem-loop primers (SLP). The technique enables detection of target DNA by either linear or exponential amplification (SLP-lRCA and SLP-eRCA) in both liquid and solid phases. For solid-phase detection, SLP-eRCA detects nucleic acids in four steps: (1) covalently immobilize an array of capture probes (CP) on a solid supp...

Journal: :Applied and environmental microbiology 2006
Fumito Maruyama Katsuji Tani Takehiko Kenzaka Nobuyasu Yamaguchi Masao Nasu

Detection of plasmid DNA uptake in river bacteria at the single-cell level was carried out by rolling-circle amplification (RCA). Uptake of a plasmid containing the green fluorescent protein gene (gfp) by indigenous bacteria from two rivers in Osaka, Japan, was monitored for 506 h using this in situ gene amplification technique with optimized cell permeabilization conditions. Plasmid uptake det...

Journal: :Nucleic Acids Research 2006
Jin Inoue Yasushi Shigemori Tsutomu Mikawa

Rolling circle amplification (RCA) of plasmid or genomic DNA using random hexamers and bacteriophage phi29 DNA polymerase has become increasingly popular in the amplification of template DNA in DNA sequencing. We have found that the mutant protein of single-stranded DNA binding protein (SSB) from Thermus thermophilus (Tth) HB8 enhances the efficiency of amplification of DNA templates. In additi...

Journal: :The Analyst 2014
Xingti Liu Qingwang Xue Yongshun Ding Jing Zhu Lei Wang Wei Jiang

A sensitive and label-free fluorescence assay for DNA detection has been developed based on cascade signal amplification combining exonuclease III (Exo III)-catalyzed recycling with rolling circle amplification. In this assay, probe DNA hybridized with template DNA was coupled onto magnetic nanoparticles to prepare a magnetic bead-probe (MNB-probe)-template complex. The complex could hybridize ...

Journal: :Chemical communications 2014
Bo Yao Yichen Liu Miyuki Tabata Huangtianzhi Zhu Yuji Miyahara

We developed a quantitative detection scheme for nucleic acids, combining solid-phase rolling circle amplification and chronocoulometry (RCA-CC). A gold electrode was directly formed on a polystyrene substrate as a cost-effective and flexible biosensor for sensitive detection of microRNA (mir-143) in blood samples.

Journal: :Molecules 2010
Lingwei Wu Quanjun Liu Zhongwei Wu Zuhong Lu

In this paper we describe an isothermal rolling-circle amplification (RCA) protocol to detect gene point mutations on chips. The method is based on an allele-specific oligonucleotide circularization mediated by a special DNA ligase. The probe is circularized when perfect complementary sequences between the probe oligonucleotide and HIV cDNA gene. Mismatches around the ligation site can prevent ...

Journal: :Journal of clinical microbiology 2014
Shuwen Deng G Sybren de Hoog Weihua Pan Min Chen A H G Gerrits van den Ende Liyue Yang Jiufeng Sun Mohammad Javad Najafzadeh Wanqing Liao Ruoyu Li

In this study, we developed rapid and sensitive assays for the detection of Cladophialophora carrionii, a common agent of human chromoblastomycosis. The isothermal techniques evaluated were rolling-circle amplification (RCA), multiplex ligation-dependent probe amplification (MLPA), and loop-mediated isothermal amplification (LAMP). The probes for RCA and MLPA were designed with target sequences...

Journal: :BioTechniques 2009
Gyanendra Kumar Galina Chernaya

Utilizing in vitro transcription and translation (IVTT) to produce small quantities of proteins is convenient but requires a significant supply of pure template DNA. This can be cumbersome, particularly when the method is used for many different templates in a high-throughput manner. Multiply-primed rolling circle amplification (RCA) with [#x03C6]29 DNA polymerase is a simple way to generate la...

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