Dts1061
The DTS1061 is a differential thermal analysis (DTA) instrument manufactured by Malvern Panalytical. It is designed to measure the thermal behavior of materials as a function of temperature and time. The DTS1061 can detect phase transitions, chemical reactions, and other thermal events in a sample.
Lab products found in correlation
22 protocols using dts1061
Zeta Potential of Pseudomonal LPS
Characterization of Magnetic Nanoparticles
The SAR of the used MNPs was determined as described elsewhere using an AMF (H =15.4 kA/m, f =435 kHz).11 (link),28 For this purpose, temperatures were acquired by a fiber optic temperature sensor and a fiber optic thermometer (TS5 and FOTEMPMK-19, both OPTOCON AG, Germany), and the relevant iron concentrations were determined in triplicates by atomic absorption spectroscopy (AAS). The SAR of immobilized MNPs, as occurring after cellular internalization and/or binding, was measured after their immobilization in polyvinyl alcohol (PVA 10%, w/v, Sigma-Aldrich).11 (link),29 (link)–31 (link) High resolution electron microscopy (HRTEM) pictures of MNPs were obtained as described elswere.11 (link)
Polyplex Characterization by DLS
Zeta Potential and Particle Size Analysis
Peptide Size Measurement in Solution
Bacterial Zeta Potential Measurements
Citrate-Stabilized Gold Nanoparticle Synthesis
Zeta Potential Measurements of Nanoparticles
Zeta Potential Analysis of Dried Powders
distributions of dried powders suspended in water were measured by
dynamic light scattering (DLS) with a Zetasizer Nano ZS (Malvern Ltd,
Worcestershire, U.K.) and were quantified by laser Doppler velocimetry
as electrophoretic mobility using a disposable electrophoretic cell
(DTS1061, Malvern Ltd., Worcestershire, U.K.). A total of 10 runs
of 30 s were performed for each measurement, and four measurements
were carried out for each sample. Zeta average values were obtained
by suspending the dry powders in the same media at a concentration
of 1.0 mg/mL. A total of 20 runs of 30 s each were performed for each
measurement and for each sample.
Characterization of MNP Formulations
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