A general method for cloning recA genes of gram-positive bacteria by polymerase chain reaction.

An internal fragment of the recA gene from eight gram-positive organisms has been amplified by using degenerate primers in a polymerase chain reaction. The internal 348- or 360-bp recA DNA segments from Bacillus subtilis, Clostridium acetobutylicum, Lactobacillus bulgaricus, Lactobacillus helveticus...

ver descrição completa

Detalhes bibliográficos

Publicado no:	J Bacteriol
Principais autores:	Duwat, P, Ehrlich, S D, Gruss, A
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 1992
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC206342/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1629178/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.174.15.5171-5175.1992
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!