Discriminative detection of low-abundance point mutations using a PCR/ligase detection reaction/capillary gel electrophoresis method and fluorescence dual-channel monitoring

2014 ◽  
Vol 35 (8) ◽  
pp. 1204-1210 ◽  
Author(s):  
Mariko Hamada ◽  
Koji Shimase ◽  
Kazuhiko Tsukagoshi ◽  
Masahiko Hashimoto
2010 ◽  
Vol 31 (3) ◽  
pp. 448-458 ◽  
Author(s):  
Nathan A. Lacher ◽  
Qian Wang ◽  
Rachel K. Roberts ◽  
Heidi J. Holovics ◽  
Serdar Aykent ◽  
...  

2004 ◽  
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Author(s):  
Elena Vasilyeva ◽  
James Woodard ◽  
Frederick R. Taylor ◽  
Matthias Kretschmer ◽  
Hans Fajardo ◽  
...  

2018 ◽  
Vol 101 (2) ◽  
pp. 601-606 ◽  
Author(s):  
Xiaofei Liu ◽  
Songyin Qiu ◽  
Xiaolin Li ◽  
Dandan Liu ◽  
Hongli Jing ◽  
...  

Abstract This study aimed to establish an event-specific multiplex PCR system using microsatellite markers and fluorescently labeled primers to detect six different genetically modified (GM) animal lines, including human lactoferrin GM cattle, human lysozyme GM cattle, human α-lactalbumin GM cattle, myostatin knockout pigs, phytase GM pigs, and ω-3 fatty acid desaturase gene GM pigs. Four different microsatellite loci for species identification, along with six GM animal-specific fragments, were selected as targets for primer design. The capillary gel electrophoresis results of multiplex PCR showed that the target fragments were amplified successfully. This high-throughput multiplex PCR detection system can be applied for the inspection and quarantine of GM animals.


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