| Literature DB >> 30507947 |
Paweł Masiewicz, Anna Brzostek, Marcin Wolański, Jarosław Dziadek, Jolanta Zakrzewska-Czerwińska.
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0043651.].Entities:
Year: 2018 PMID: 30507947 PMCID: PMC6277100 DOI: 10.1371/journal.pone.0208565
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 4PrpR binds the promoter region of prpDC and icl1 genes in intact M. tuberculosis cells.
Identification of intracellular PrpR-DNA complex using immunoprecipitation. PrpR-DNA complexes cross-linked with glutaraldehyde were immunoprecipitated with anti-6HisPrpRMt polyclonal antibodies (sample 1). PCR was carried out with the primer pairs, p1129_Fw and p1129_Rv (pprpDR)(A); picl_Fw and picl_Rv (picl1)(B); and pmtrA_Fw and pmtrA_Rv (pmtrA, negative control)(C). Negative control (2) consisted of DNA template extracted from the cells subjected to immunoprecipitation, but nucleoprotein complexes were not previously cross-linked. Positives controls (+) were also performed using template obtained from strains subjected only to cross-linking (3) or total DNA extracted from the cells (4).