scholarly journals A simple DNA extraction method suitable for PCR detection of genetically modified maize

2007 ◽  
Vol 87 (14) ◽  
pp. 2728-2731 ◽  
Author(s):  
Manuel Porcar ◽  
Silvia Ramos ◽  
Amparo Latorre
2016 ◽  
Vol 8 (1) ◽  
pp. 136-141 ◽  
Author(s):  
Eric Gonzalez Garcia ◽  
Andreas H. Farnleitner ◽  
Robert L. Mach ◽  
Rudolf Krska ◽  
Kurt Brunner

A simple, solvent-free extraction method for DNA facilitates the analysis for genetically modified organisms.


2008 ◽  
Vol 49 (2) ◽  
pp. 63-69 ◽  
Author(s):  
Kiyomi OHMORI ◽  
Hisayo TSUCHIYA ◽  
Takahiro WATANABE ◽  
Hiroshi AKIYAMA ◽  
Tamio MAITANI ◽  
...  

2016 ◽  
Vol 5 (08) ◽  
pp. 4754
Author(s):  
Tanushree Mitra* ◽  
Shivshankar Kumdale ◽  
Sameer Chowdhary ◽  
Amol D. Raut

The main objective of this study was to make sure whether randomly taken 12 samples were sensitive to abacavir. The genomic DNA from 12 blood sample were extracted by phenol chloroform DNA extraction method, extracted genomic DNA were amplified and sequenced, thereafter SNPs were detected. Every sample had shown the presence of normal base at SNP position. This study indicated, those randomly taken 12 patients were sensitive to abacavir, so they can consume abacavir if they get infected with HIV.


2011 ◽  
Vol 45 (16) ◽  
pp. 5211-5217 ◽  
Author(s):  
Arine Fadzlun Ahmad ◽  
James Lonnen ◽  
Peter W. Andrew ◽  
Simon Kilvington

Microbiome ◽  
2014 ◽  
Vol 2 (1) ◽  
pp. 19 ◽  
Author(s):  
Agata Wesolowska-Andersen ◽  
Martin Bahl ◽  
Vera Carvalho ◽  
Karsten Kristiansen ◽  
Thomas Sicheritz-Pontén ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (1) ◽  
pp. e0169877 ◽  
Author(s):  
Anna Vesty ◽  
Kristi Biswas ◽  
Michael W. Taylor ◽  
Kim Gear ◽  
Richard G. Douglas

2021 ◽  
Author(s):  
Maria Iasmina Moza ◽  
Carmen Postolache

AbstractMolecular biology protocols have been more and more accessible to researchers for ecological investigations, however, these protocols always require optimization steps for the analysis of specific types of samples. The purpose of this study was to optimize a molecular protocol for the analysis of cyanobacterial 16S rRNA in Danube Delta shallows lakes. In this regard, several commercial DNA extraction kits were tested in comparison with potassium ethyl xanthogenate extraction method on different matrices. The obtained DNA was further used for 16S rRNA PCR optimization. Finally, an optimized protocol is proposed for the molecular analysis of cyanobacteria group in freshwater samples. The best DNA extraction method was the potassium xanthogenate extraction from dried cyanobacterial biomass. A dynamic in total genomic eDNA was observed, reflecting the seasonal difference in phytoplankton biomass from the studied lakes. The PCR protocol optimized by us can be successfully applied for the identification of a broad range of cyanobacterial genetic markers.


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