Dissection of a replication origin of Xenopus DNA.

A previously cloned 503-base pair (bp) EcoRI segment of genomic DNA from Xenopus laevis selected for enhancement of replication of its vector plasmid was moved to the EcoRI site of pBR322. This plasmid designated pJCC31 and five other clones, which were made by cleaving the 503-bp segment in relatio...

ver descrição completa

Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Chambers, J C, Watanabe, S, Taylor, J H
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1982
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC346946/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6752953/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.18.5572
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!