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Differentiation of Chlamydia spp. by sequence determination and restriction endonuclease cleavage of RNase P RNA genes.

The amplification of DNA from Chlamydia trachomatis by PCR with degenerated primers yielded a 345-bp fragment of the putative RNase P RNA gene. From the deduced DNA sequence of this gene in C. trachomatis, a modified primer pair was designed. The primer pair was subsequently used to obtain the corre...

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Pubblicato in:J Clin Microbiol
Autori principali: Herrmann, B, Winqvist, O, Mattsson, J G, Kirsebom, L A
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Microbiology (ASM) 1996
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Accesso online:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC229149/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8818877/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jcm.34.8.1897-1902.1996
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