학술저널
Detection for heat-labile enterotoxin(LT) of enterotoxigenic Escherichia coli(ETEC) by use of the reversed passive latex agglutination(RPLA) was positive reaction from 2-fold(50 ng/ml) to 64-fold dilutions in EC81 and EC83. The polymerase chain reaction(PCR) which was using LT gene-specific primers of ETEC with a detection limit equivalent from 1 ng/㎕ to 1 pg of a DNA fragment of 417-bp in EC81 and EC83. The PCR provided a rapid and more sensitivity tool for the detecting LT of ETEC compare to the RPLA.
I. 서론
II. 실험재료 및 방법
III. 결과 및 고찰
IV. 결론
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