| Literature DB >> 28826394 |
Abstract
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Year: 2017 PMID: 28826394 PMCID: PMC5567570 DOI: 10.1186/s12866-017-1072-9
Source DB: PubMed Journal: BMC Microbiol ISSN: 1471-2180 Impact factor: 3.605
Fig. 6Presentation of the antigenic tags on gp9 of phage particles. (a) M13 phage (panel a) was applied onto nitrocellulose membrane and incubated with antibody to gp8, T7tag and HA tag, respectively, at the indicated concentrations. To visualize the phage a peroxidase-linked secondary antibody was applied and analysed by chemoluminescence. b M13 am9 phage grown in E. coli K38 cells bearing a plasmid encoding gp9-T7 or gp9DT7, respectively, were incubated with antibody to T7 and treated as described above. c M13 am9 phage propagated in E. coli K38 cells bearing a plasmid encoding gp9-HA or gp9DHA, respectively, were incubated with antibody to HA and treated as described above. For controls (Ctr), uninfected cultures were tested under identical conditions.