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Toledo delta 320 ph meter

Manufactured by Mettler Toledo
Sourced in Switzerland

The Toledo Delta 320 pH meter is a compact and user-friendly device designed to measure the pH of various solutions. It features a digital display for easy readability and provides accurate pH measurements. The meter comes equipped with standard electrodes for reliable performance in a laboratory setting.

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3 protocols using toledo delta 320 ph meter

1

Synthesis and Characterization of Organic Compounds

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Reagents were purchased from Adamas (Basel, Switzerland), Acros (Pittsburgh, PA, USA), TCI (Tokyo, Japan), Sigma-Aldrich (St. Louis, MO, USA), and SCRC (Shanghai, China). All reagents were of analytical grade and obtained from commercial suppliers. Dichloromethane (CH2Cl2) was distilled over calcium hydride. Triethylamines were stored with molecular sieves (4A) before use. The water used in all experiments was purified using a Millipore Milli-Q water system (Billerica, MA, USA). 1H NMR (400 MHz) spectra were recorded on a Bruker Ascend 400 (Fällanden, Switzerland) in CDCl3 as a solvent with TMS as the internal standard. UV–vis absorption spectra were recorded on a Shimadzu UV-1800 spectrometer (Kyoto, Japan) in 1.0 cm path-length quartz. Fluorescence spectra were recorded on an Agilent Cary eclipse fluorometer (Santa Clara, CA, USA) with both excitation and emission slits set at 5 nm. The pH value measurements were carried out with a Mettler Toledo Delta 320 pH meter (Zurich, Switzerland). The fluorescence microscopy images of plant tissue were recorded with an Olympus CKX53 fluorescence microscope (Tokyo, Japan). Whole-plant real-time images were recorded with ImagingPhotonIMAGER (Paris, France). All experiments were performed in flame-dried glassware using dry solvents unless otherwise noted.
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2

Evaluating Platelet Concentrate Storage

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Sampling was done by stripping the tubing of the PC bag to ensure the uniform mixing of PC. The PC was then collected from the tubing segment into a plain tube (as the specimen was already in an anticoagulated form). All the measurements were done on day 1, day 5, and day 8 of the storage period, except for the sterility test, that was carried out only once on the last day, i.e., the eighth day of storage. The total platelet count and total WBC count were determined using standard calibrated hematology analyzer (Beckman Coulter LH750, CA, United States). The pH was measured using pH meter (Mettler Toledo Delta 320 pH meter). Sterility test was performed using automated blood culture system (Organon Teknika). Platelet activation marker was measured by expression of CD62p marker using flow cytometer (FACSCalibur of Becton Dickinson).
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3

Cell Pellet Washing and Resuspension

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After 15 hours of incubation, 2.5 mL of culture broth was withdrawn and diluted with 37.5 mL of non-sterile wash buffer in a 50 mL polypropylene centrifuge tube and mixed vigorously by hand and vortex mixer. This content was centrifuged at 3300 x g for 10 minutes at 25 o C. Following centrifugation, wash buffer was carefully decanted off without disturbing the cell pellet. 40 mL of wash buffer was added to the centrifuge tube and the contents resuspended by vigorous mixing by hand and vortex mixer. The centrifugation and washing steps were repeated a total of three times prior to use of 40 mL of deionized water for resuspending the cell pellet through vigorous shaking by hand and vortex mixer. Nitric acid and sodium hydroxide was added to the samples for pH adjustment with pH measured by an Orion 9156 BNWP pH probe outfitted to a Mettler Toledo Delta 320 pH meter.
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