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Journal of Preventive Medicine ; : 65-70, 2003.
Artigo em Vietnamita | WPRIM | ID: wpr-6134

RESUMO

In this study, PCR technique was used with 2 primer pairs for amplifying DNA fragments at 5’ and 3’ of the gene encoding diphteria toxine of the strains Corynebacterium diphtheriae. After the cloning and sequencing, 2 separated fragments were joined to form a complete gene. The sequence of gene was translated into protein and the results were submitted into Gene Bank Database


Assuntos
Toxina Diftérica , Genes , Corynebacterium diphtheriae
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