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Zetasizer nano zs90 device

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Zetasizer Nano ZS90 is a dynamic light scattering (DLS) device used for the measurement of particle size and zeta potential. It is capable of characterizing particles, molecules, and colloids with sizes ranging from 0.3 nanometers to 10 micrometers.

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2 protocols using zetasizer nano zs90 device

1

Measles Virus Stability Assay

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The clarified MV suspension was diluted 1:10 with 20 mM Tris-HCl (pH 7.5–9.0) or 20 mM citrate-phosphate buffer (pH 3.0–7.0) in steps of 0.5 along the pH scale for the used buffers. Experiments were conducted at room temperature and in triplicates. The infectivity of the virus was determined as above immediately after mixing the virus suspension with the buffer or after incubation for 1 h at room temperature followed by freezing at –80 °C. A suspension of MV diluted 1:10 in 20 mM Tris-HCl (pH 7.4) was used as a positive control.
The size distribution of the MV particles was investigated by dynamic light scattering (DLS) using a Zetasizer Nano ZS90 device (Malvern Instruments, Malvern, UK) and a low-volume cuvette (Sarstedt, Sarstedt, Germany). The suspension was stored on ice and mixed with buffer immediately before the initial measurement, and the measurement was repeated after incubation for 1 h at room temperature.
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2

Measuring Zeta Potential in Bacterial Strains

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Overnight cultures were started as described in Etest section above. Since media composition (salt concentration and pH) can affect zeta potential, [67 (link)], 0.5 mL of each culture was washed in 1X PBS and resuspended in 1 mL 0.1X PBS diluted in sterile nanopure water to minimize media influence on these measurements. We also report conductivity measurements to show that salt concentration has been normalized by this procedure. The Zeta potential was measured on a Malvern Zetasizer Nano ZS90 device (Malvern) at room temperature 25°C. Zeta potential standards were obtained from Malvern (DTS1235, –42 mV ± 4.2 mV) and used according to the manufacturer’s instructions. Measurements were performed in Zetasizer folded capillary cells (DTS1070, Malvern) in triplicate reads (n = 3). Values given are mean ± standard deviation. Zeta potential assays were repeated on at least two separate occasions. GraphPad Prism version 8 was used to perform a two-way ANOVA with Tukey’s multiple comparison test to compare UGA strains 10 and 14 to the antimicrobial susceptible strain ATCC 13311 (*P < 0.05, **P < 0.01, ***P < 0.001).
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