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Borosilicate glass tubes

Manufactured by Thermo Fisher Scientific

Borosilicate glass tubes are laboratory equipment designed for a variety of scientific applications. They are made from a specialized type of glass that is resistant to thermal shock and chemical corrosion, making them suitable for a wide range of experiments and procedures. These tubes provide a durable and reliable containment solution for liquids, gases, and other materials used in laboratory settings.

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3 protocols using borosilicate glass tubes

1

Analytical Protocol for Cyanotoxin Detection

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Methanol, acetonitrile, formic acid, ammonium formate, and water (all LC/MS or Optima grade) were obtained from Fisher Chemicals (Fair Lawn, NJ, USA). Ammonium hydroxide (NH3 content 28–30%; analytical grade) was from Sigma-Aldrich (St. Louis, MO). Solid phase extraction (SPE) cartridges were 60-mg Oasis HLB with 30-µm particle size (Waters, Milford, MA). Borosilicate glass tubes, autosample vials, and polypropylene centrifuge tubes were purchased from Fisher Scientific. Milli Q water (>18 MΩ) was produced from a water purification system (Barnstead Nanopure). Multi-anion standards were from Sigma-Aldrich (St. Louis, MO, USA) and multi-cation standards were from Alltech (USA). Anatoxin-a, microcystin-LA, -LR, and -RR standards, as well as saxitoxin and cylindrospermopsin ELISA kits were all from Abraxis (Warminster, PA, USA). The 25-mm glass microfiber GF/A syringe filters were obtained from Whatman (GE Healthcare UK Limited, UK) and B-D 10-mL disposable syringes were from Becton Dickinson & Co (Franklin Lakes, NJ, USA). The IC eluents were sodium hydroxide (50%, w/w) for anion analysis and methanesulfonic acid for cation analysis.
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2

Quantifying Clostridium perfringens Growth

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A total of 74 hyper-immune sera were developed against 37 different peptides. Each serum was tested in replicates of 5, with 3 replicate experiments, and all data are presented as a composite of replications. In sterile borosilicate glass tubes (12 × 75 mm; Fisher Scientific, Hampton, NH), 10 µ L of 1 × 106 CFU/mL of CP was added to 1 mL of 0.5X Luria-Bertani broth (Becton and Dickenson, Sparks, MD) containing 1.00% porcine stomach mucin (Sigma Aldrich, St. Louis, MO) and 20 µ L of chicken hyper-immune serum for a final concentration of 1 × 104 CFU/mL of CP in each tube. All tubes were then incubated in anaerobic jars at 37°C. At the 4, 6, and 8 h marks of incubation, samples were collected for quantification of CFU by serial dilution plating on tryptic soy agar (TSA) with 0.25% sodium thioglycolate (VWR, Radnor, PA) and incubated in anaerobic jars at 37°C for 24 h. Growth (CFU/mL) of CP was calculated as a sample over negative ratio relative to the mean negative control and converted to a percentage.
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3

Comprehensive Cannabinoid Standard Preparation

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Stocks of 1 mg/mL of CBD, THC, CBN, 11-OH-THC, CBG, THCV, THCA-A, and THCCOOH-D 3 as well as 100 μg/mL solutions of THCCOOH, THCCOOH-gluc, CBD-D 3 , THC-D 3 , CBN-D 3 , and 11-OH-THC-D 3 were purchased from Cerilliant (Round Rock, TX, USA). A 10-μg/mL THCgluc stock was obtained from ElSohly (Oxford, MS, USA).
Optima LC/MS grade acetonitrile, methanol, 2-propanol, formic acid (FA), and ammonium acetate were obtained from Fisher Scientific (Hampton, NH, USA). Oasis PRiME HLB 96-well solid-phase extraction (SPE) plates with 30 mg sorbent/well, 96-well collection plates, quick-load glass inserts, silicone/PTFE-treated 96-well square plug cap mats, and amber max recovery autosampler vials were acquired from Waters (Milford, MA, USA). Borosilicate glass tubes were from Fisher Scientific and 18.2 MΩ-cm water was dispensed from a Siemens PureLab Ultra purification system.
Blank WB was created by mixing acid citrate dextrose (ACD)packed red blood cells with ABO-compatible plasma and confirming the absence of detectable cannabinoids. Breath matrix consisted of an unused SensAbues ® electret filter material ("pad") cut into 28 cm 2 squares to match the intake surface area of the SensAbues ® collection device.
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