epidermidis. At least, sufficient concentration for amplifying was 5 ng/ L of DNA of S. epidermidis. Also, in this study gold nanoparticles probes were used for colorimetric detection of S. epidermidis. Two 20-base thiolated probes were prepared based on the sequence of pta housekeeping gene of S. epidermidis. Genomic DNA of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Acinetobacter baumannii were used as negative controls and no alteration was detected. To investigate the sensitivity of the gold nanoparticles probes, we used different concentrations of the extracted DNA from S. epidermidis. At least, sufficient concentration for alteration color and absorption of solution was 15 ng/ L. Our results revealed that both methods were sufficiently specific and sensitive to detect S.
epidermidis. At least, sufficient concentration for amplifying was 5 ng/ L of DNA of S. epidermidis. Also, in this study gold nanoparticles probes were used for colorimetric detection of S. epidermidis. Two 20-base thiolated probes were prepared based on the sequence of pta housekeeping gene of S. epidermidis. Genomic DNA of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Acinetobacter baumannii were used as negative controls and no alteration was detected. To investigate the sensitivity of the gold nanoparticles probes, we used different concentrations of the extracted DNA from S. epidermidis. At least, sufficient concentration for alteration color and absorption of solution was 15 ng/ L. Our results revealed that both methods were sufficiently specific and sensitive to detect S.