Building a better mousetrap for accurate and sensitive polymerase chain reaction

Author(s):  
Jerry Radich ◽  
Fred Hutch
2006 ◽  
Vol 8 (10) ◽  
pp. 628-634 ◽  
Author(s):  
Bradford Coffee ◽  
Kasinathan Muralidharan ◽  
William E Highsmith ◽  
Pablo Lapunzina ◽  
Stephen T Warren

2005 ◽  
Vol 88 (5) ◽  
pp. 1394-1398 ◽  
Author(s):  
Ying Chen ◽  
Ya-Jun Wu ◽  
Bao-Liang Xu ◽  
Jing Wan ◽  
Zeng-Ming Qian

Abstract A sensitive polymerase chain reaction (PCR) method based on amplification of a specific DNA fragment was established for the identification of camel (Camelus) materials. The species-specific primer pair L183/H372 was designed based on the nucleotide sequence of the mitochondrial cytochrome b gene, and its specificity was confirmed by amplification of 3 camel (domestic double-humped camel, wild double-humped camel, wild one-humped camel) samples and 11 non-Camelus animal (sheep, goat, pig, chicken, cattle, fish, dog, horse, donkey, deer, and rabbit) materials. An expected 208 base pair fragment was amplified from camel materials; no cross-reactive or additional fragments were generated from other animal materials. Taq I restriction endonuclease digestion of the unpurified PCR product can be used routinely to confirm the camel origin of the amplified sequence.


Transfusion ◽  
2007 ◽  
Vol 47 (10) ◽  
pp. 1756-1764 ◽  
Author(s):  
Steven H. Kleinman ◽  
Simone A. Glynn ◽  
Tzong-Hae Lee ◽  
Leslie Tobler ◽  
Leilani Montalvo ◽  
...  

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