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Cpc200

Manufactured by Bangs Laboratories
Sourced in United States

The CPC200 is a compact power supply unit designed for powering a variety of laboratory equipment. It provides a stable and regulated output voltage to support the operation of various instruments and devices used in research and testing environments.

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3 protocols using cpc200

1

Carboxylated Polystyrene Particle Preparation

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Carboxylated polystyrene particles, denoted as CPC200, with a mean nominal diameter of 210 nm and stock concentration of 1 × 1012 particles/mL, were purchased from Bangs Laboratories, USA and used as a calibrant for zeta potential analysis, as well as the sample particles. CPC200s were vortexed for 30 s followed by a 2 min sonication to ensure monodispersity prior to any TRPS analysis or sample incubation.
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2

Carboxylated Polystyrene Particle Standards

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Carboxylated polystyrene particle standards with a nominal mean diameter of 210 nm, denoted as CPC200, were purchased from Bangs Laboratories (Fishers, IN, USA). CPC200 were diluted in PBS (137 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, 1.8 mM K2HPO4)+(0.03% w/v Tween 20) at a concentration of 6.7×109/ml and shipped to the 6 trial participants. The CPC200 suspension was mixed with double-strength PBS in a 1:1 ratio (v/v) to make a single-strength solution just before evaluation with TRPS by qNano (Izon Science).
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3

Characterizing Nanoparticles with qNano

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TRPS was performed using the qNano system (IZON Sciences, New Zealand) with the IZON Control Suite software (V3.1.2.53). NP100, NP200 or NP300 elastomeric tuneable nanopores were used, suitable for analysing beads between 85 and 600 nm (as stated by the manufacturer). Carboxylated polystyrene beads, denoted as CPC200 (Bangs Laboratories, USA), with a mean nominal diameter of 210 nm and stock concentration of 1 × 1012 particles/ml, were used as a concentration calibrant at 2 × 109/ml. Prior to use, the beads were vortexed for 30 s and sonicated for 1 min to ensure mono-dispersity. An appropriate stretch and a voltage was applied throughout so that the blockades of CPC200s in PBS were at least 0.5 nA above the background noise. The qNano was operated as previously described [38 (link)]. Briefly, the lower fluid cell was filled with 75 μl of PBS, ensuring no air bubbles are present and the upper fluid cell contained 40 μl of sample. After each measurement, the sample was removed from the upper fluid cell and replaced with PBS. This was repeated several times, applying varying amounts of pressure and vacuum, until visible blockades were observed.
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