2019
DOI: 10.1007/s12275-019-8610-0
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Lytic KFS-SE2 phage as a novel bio-receptor for Salmonella Enteritidis detection

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Cited by 11 publications
(12 citation statements)
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“…An aliquot of 10 µL of the filtrate was dotted on the surface of pre-solidified TA soft agar (4 g agar, 8 g nutrient broth, 5 g NaCl, 0.2 g MgSO 4 , 0.05 g MnSO 4 , and 0.15 g CaCl 2 per 1 L) containing 200 µL of the indicator strain suspension. The presence of phages in the filtrate was then confirmed using a dot assay [ 9 ]. Once the formation of a clear zone was observed, a plaque assay was performed to isolate single phages from the filtrate.…”
Section: Methodsmentioning
confidence: 99%
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“…An aliquot of 10 µL of the filtrate was dotted on the surface of pre-solidified TA soft agar (4 g agar, 8 g nutrient broth, 5 g NaCl, 0.2 g MgSO 4 , 0.05 g MnSO 4 , and 0.15 g CaCl 2 per 1 L) containing 200 µL of the indicator strain suspension. The presence of phages in the filtrate was then confirmed using a dot assay [ 9 ]. Once the formation of a clear zone was observed, a plaque assay was performed to isolate single phages from the filtrate.…”
Section: Methodsmentioning
confidence: 99%
“…After incubation for 16 h at 37°C, each plaque was picked with a customized tip and eluted with sodium chloride-magnesium sulphate (SM) buffer (50 mM Tris-HCl, 100 mM NaCl, 10 mM MgSO 4 , pH 7.5) with vigorous agitation for 1 h at 22°C. All of these procedures were repeated until the single phage was isolated [ 9 ]. To increase of the concentration of the single phage, 3 mL of TA broth containing 1% (v/v) indicator strain suspension was incubated for 2.5 h at 37°C.…”
Section: Methodsmentioning
confidence: 99%
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