Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2021 Mar 16;11:6001. doi: 10.1038/s41598-021-85438-5

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Full characterisation of Enterococcus faecium (a), Acinetobacter baumannii (b), Enterococcus cloacae (c), and Staphylococcus aureus (d) isolates, comprising identification (black) via 16S rRNA genes and characterisation in terms of ABR genes (red/blue/green/orange) and VFs (magenta and related colors). The DNA of a clinical isolate carrying the specified pathogen was purified and amplified by multiplex PCRs including the primer pairs of all investigated genes. The amplification products were applied to the microarray chips along with detection oligonucleotides. If matching, the detection oligonucleotides could be ligated to the probes and subsequently detected by a standard fluorescence-based microarray scanner.