Quantitation of 35S promoter in maize DNA extracts from genetically modified organisms using real-time polymerase chain reaction, part 2: Interlaboratory study

被引:0
|
作者
机构
[1] Feinberg, Max
[2] Fernandez, Sophie
[3] Cassard, Sylvanie
[4] Charles-Delobel, Hrystèle
[5] Bertheau, Yves
[6] Balois, A.M.
[7] Cassard, S.
[8] Charles, C.
[9] Diolez, A.
[10] Gachet, E.
[11] Gavard, P.
[12] Hauser, S.
[13] Lacotte, K.
[14] Le Bouquin, R.
[15] Martin, E.
[16] Minvielle, A.C.
[17] Petit, L.
[18] Rousselin, P.
[19] Skorski, G.
[20] Zhang, D.
来源
Feinberg, M. (feinberg@inapg.inra.fr) | 1600年 / AOAC International卷 / 88期
关键词
Crops;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [31] A cotton-specific gene, stearoyl-ACP desaturase, used as a reference for qualitative and real-time quantitative polymerase chain reaction detection of genetically modified organisms
    Xu, Wen-Tao
    Huang, Kun-Lun
    Wang, Ying
    Zhang, Hong-Xing
    Luo, Yun-Bo
    JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2006, 86 (07) : 1103 - 1109
  • [32] Detection of mitochondrial DNA from human inner ear using real-time polymerase chain reaction and laser microdissection
    Kimura, Y
    Kouda, H
    Eishi, Y
    Kobayashi, D
    Suzuki, Y
    Ishige, I
    Iino, Y
    Kitamura, K
    ACTA OTO-LARYNGOLOGICA, 2005, 125 (07) : 697 - 701
  • [33] Inter laboratory Validation Study of an Event-Specific Real-time Polymerase Chain Reaction Detection Method for Genetically Modified 55-1 Papaya
    Noguchi, Akio
    Nakamura, Kosuke
    Sakata, Kozue
    Kobayashi, Tomoko
    Akiyama, Hiroshi
    Kondo, Kazunari
    Teshima, Reiko
    Ohmori, Kiyomi
    Kasahara, Masaki
    Takabatake, Reona
    Kitta, Kazumi
    JOURNAL OF AOAC INTERNATIONAL, 2013, 96 (05) : 1054 - 1058
  • [34] Primer rRNA-12S for detection of bovine gelatine DNA in capsule shells using real-time polymerase chain reaction
    Fitriani, N. F.
    Sudjadi
    Rohman, A.
    INTERNATIONAL FOOD RESEARCH JOURNAL, 2018, 25 (05): : 1870 - 1875
  • [35] Evaluation of pathogen detection from clinical samples by real-time polymerase chain reaction using a sepsis pathogen DNA detection kit
    Yanagihara, Katsunori
    Kitagawa, Yuko
    Tomonaga, Masao
    Tsukasaki, Kunihiro
    Kohno, Shigeru
    Seki, Masafumi
    Sugimoto, Hisashi
    Shimazu, Takeshi
    Tasaki, Osamu
    Matsushima, Asako
    Ikeda, Yasuo
    Okamoto, Shinichiro
    Aikawa, Naoki
    Hori, Shingo
    Obara, Hideaki
    Ishizaka, Akitoshi
    Hasegawa, Naoki
    Takeda, Junzo
    Kamihira, Shimeru
    Sugahara, Kazuyuki
    Asari, Seishi
    Murata, Mitsuru
    Kobayashi, Yoshio
    Ginba, Hiroyuki
    Sumiyama, Yoshinobu
    Kitajima, Masaki
    CRITICAL CARE, 2010, 14 (04)
  • [36] Quantifying Neodiprion sertifer nucleopolyhedrovirus DNA from insects, foliage and forest litter using the quantitative real-time polymerase chain reaction
    Krokene, Paal
    Heldal, Inger
    Fossdal, Carl G.
    AGRICULTURAL AND FOREST ENTOMOLOGY, 2013, 15 (02) : 120 - 125
  • [37] Evaluation of pathogen detection from clinical samples by real-time polymerase chain reaction using a sepsis pathogen DNA detection kit
    Katsunori Yanagihara
    Yuko Kitagawa
    Masao Tomonaga
    Kunihiro Tsukasaki
    Shigeru Kohno
    Masafumi Seki
    Hisashi Sugimoto
    Takeshi Shimazu
    Osamu Tasaki
    Asako Matsushima
    Yasuo Ikeda
    Shinichiro Okamoto
    Naoki Aikawa
    Shingo Hori
    Hideaki Obara
    Akitoshi Ishizaka
    Naoki Hasegawa
    Junzo Takeda
    Shimeru Kamihira
    Kazuyuki Sugahara
    Seishi Asari
    Mitsuru Murata
    Yoshio Kobayashi
    Hiroyuki Ginba
    Yoshinobu Sumiyama
    Masaki Kitajima
    Critical Care, 14
  • [38] Improved quantitation of minimal residual disease in multiple myeloma using real-time polymerase chain reaction and Plasmid-DNA complementarity determining region III standards
    Gerard, CJ
    Olsson, K
    Ramanathan, R
    Reading, C
    Hanania, EG
    CANCER RESEARCH, 1998, 58 (17) : 3957 - 3964
  • [39] A method for correcting standard-based real-time PCR DNA quantitation when the standard's polymerase reaction efficiency is significantly different from that of the unknown's
    Irwin, Peter L.
    Nguyen, Ly-Huong T.
    Chen, Chin-Yi
    Uhlich, Gaylen A.
    Paoli, George C.
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2012, 402 (09) : 2713 - 2725
  • [40] A method for correcting standard-based real-time PCR DNA quantitation when the standard’s polymerase reaction efficiency is significantly different from that of the unknown’s
    Peter L. Irwin
    Ly-Huong T. Nguyen
    Chin-Yi Chen
    Gaylen A. Uhlich
    George C. Paoli
    Analytical and Bioanalytical Chemistry, 2012, 402 : 2713 - 2725