Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Shinya Kurata"'
Autor:
Shinya Kurata, Yasufumi Matsumura, Yasushi Enomoto, Hiroshi Habe, Tetsuya Nakazato, Hidenori Tani, Masahiro Yamaguchi
Publikováno v:
Analytical Biochemistry. 617:114114
We developed a novel nanocomposite bead system for detection by the naked eye of specific DNA sequences amplified by the polymerase chain reaction (PCR). The DNA probes, which were complementary to the target DNA, are conjugated with the nanocomposit
Publikováno v:
Nucleic Acids Research
Ribosomes, after one round of translation, must be recycled so that the next round of translation can occur. Complete disassembly of post-termination ribosomal complex (PoTC) in yeast for the recycling consists of three reactions: release of tRNA, re
Autor:
Shinya Kurata, Satoshi Tsuneda, Toyokazu Yokomaku, Takeshi Terahara, Shigeaki Harayama, Kazutaka Yamada
Publikováno v:
Enzyme and Microbial Technology. 47:17-23
Putative esterase genes were isolated from environmental DNA by using pre-amplified inverse PCR. The sequence analysis of the isolated genes showed 32–80% amino acid sequence identities to known esterases/lipases in public databases. The isolated g
Autor:
Ryo Miyata, Yuji Sekiguchi, Ken Adachi, Hidenori Tani, Shinya Kurata, Naohiro Noda, Kazunori Nakamura, Satoshi Tsuneda
Publikováno v:
Molecular and Cellular Probes. 24:131-137
Dehalococcoides spp. are responsible for the reductive dehalogenation of environmental contaminants and are candidates for engineered bioremediation. The development of a sensitive, reliable, and rapid method for the quantification of Dehalococcoides
Publikováno v:
Proceedings of the National Academy of Sciences. 107:10854-10859
After each round of protein biosynthesis, the posttermination complex (PoTC) consisting of a ribosome, mRNA, and tRNA must be disassembled into its components for a new round of translation. Here, we show that a Saccharomyces cerevisiae model PoTC wa
Autor:
Satoshi Tsuneda, Naohiro Noda, Kazunori Nakamura, Yuji Sekiguchi, Shinya Kurata, Ryo Miyata, Kouhei Ichikawa, Hidenori Tani, Soji Morishita
Publikováno v:
Analytical Chemistry. 81:5678-5685
We have developed a flexible, specific, and cost-effective real-time polymerase chain reaction (PCR) method. In this technique, a quenching probe (QProbe) and a nonfluorescent 3'-tailed probe are used. The QProbe is a singly labeled oligonucleotide b
Autor:
Soji Morishita, Yuji Sekiguchi, Shinya Kurata, Satoshi Tsuneda, Naohiro Noda, Kazunori Nakamura, Hidenori Tani
Publikováno v:
Clinical Biochemistry. 42:515-520
Objectives This study developed a novel MRD monitoring method targeting Wilms' tumor gene (WT1) mRNA using reverse transcription loop-mediated isothermal amplification (RT-LAMP). Design and methods A primer set for the assay was designed on the basis
Autor:
A. Manome, Shinya Kurata, T. Yokomaku, Yoichi Kamagata, O. Koyama, Takahiro Kanagawa, A. Kageyama, Hideyuki Tamaki, Masahiro Tagawa
Publikováno v:
Plant Pathology. 57:887-896
Common scab of potato tubers caused by pathogenic Streptomyces spp. is a cause of serious economic loss worldwide. For the rapid and accurate quantification of pathogenic Streptomyces spp. residing in soil, a new competitive real-time PCR method usin
Autor:
Takashi Ohtsuki, Kimitsuna Watanabe, Kazuyuki Takai, Takeshi Wada, Venki Ramakrishnan, Shinya Kurata, Albert Weixlbaumer, Tomomi Shimazaki, Tsutomu Suzuki, Yohei Kirino
Publikováno v:
Journal of Biological Chemistry. 283:18801-18811
Post-transcriptional modifications at the first (wobble) position of the tRNA anticodon participate in precise decoding of the genetic code. To decode codons that end in a purine (R) (i.e. NNR), tRNAs frequently utilize 5-methyluridine derivatives (x
Autor:
Toyokazu Yokomaku, Shigeaki Harayama, Shinya Kurata, Takeshi Terahara, Kazutaka Yamada, Satoshi Tsuneda
Publikováno v:
Environmental Microbiology
Summary We had been unsuccessful to amplify desired nucleotide sequences from various environmental DNA samples by using the inverse polymerase chain reaction (IPCR) technique, most probably because the copy numbers of target DNA sequences had been q