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Heparinized tubes

Manufactured by Thermo Fisher Scientific

Heparinized tubes are specialized laboratory containers used for the collection and storage of blood samples. Their primary function is to prevent the coagulation or clotting of the collected blood, allowing for accurate analysis and testing of the sample.

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5 protocols using heparinized tubes

1

Virus Tissue Harvesting and Quantification

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Serum, lung, liver, and kidneys were harvested from Cl-13-infected mice. Serum was isolated from whole blood collected in heparinized tubes (Fisher; Pittsburgh, PA), capped (Lecia Microsystems; Richmond, IL) and spun at 2500 rpm for 30 min. Serum was collected and snap-frozen in liquid nitrogen prior to storage at -80°C. Lung, liver and kidneys were homogenized and processed for plaque assays as previously described [48 (link)].
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2

Plasma Metabolite Analysis in Fed Mice

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Approximately 20 µl of whole blood was obtained by submandibular bleed at 9–10 a.m. from mice in a fed state. Blood was collected on ice using heparinized tubes (Fisherbrand) and plasma was isolated by centrifugation for 20 min at 2000 × g at 4 °C, aliquoted, and frozen at −80 °C until time of assay. Plasma leptin concentration was measured using mouse leptin ELISA (R&D) with sensitivity of 22 pg/ml. Plasma insulin concentration was measured using mouse insulin ELISA (Mercodia) and plasma glucose was measured with Autokit Glucose (WAKO).
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3

Plasma Collection and Metabolic Analysis

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Blood was collected on ice using heparinized tubes (Fisherbrand). Plasma was isolated by centrifugation for 20 min at 2,000 x g at 4°C and frozen at −80°C until assay. Mice were bled at 11 weeks of age prior to transfer to the calorimeters (Fig 1). Blood from CR mice was collected before feeding (fasted overnight) while AL group was bled in a fed state. Insulin was assayed using Rat/Mouse ELISA kit (Mercodia) and glucose using Autokit Glucose (Wako).
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4

Plasma Biomarker Measurements in Mice

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Approximately 20 ul of whole blood was obtained by submandibular bleed at 9–10 am from mice in a fed state. Blood was collected on ice using heparinized tubes (Fisherbrand) and plasma was isolated by centrifugation for 20 min at 2,000 × g at 4°C, aliquoted, and frozen at −80°C until time of assay. Plasma leptin concentration was measured using mouse leptin ELISA (R&D) with sensitivity of 22 pg/ml. Plasma insulin concentration was measured using mouse insulin ELISA (Mercodia) and plasma glucose was measured with Autokit Glucose (WAKO).
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5

Evaluating Liver Toxicity in Mice

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C57BL/6J mice (n = 5–7) were treated i.v. with CPMV, CPMV‐H6, CPMV‐G3, H6, G3, or PBS (200 mg CPMV per mouse; the peptide dose was normalized to match the number of peptides delivered by CPMV). After 1, 3, and 7 days, blood was collected through retroorbital bleeds using heparinized tubes (Fisher Scientific). The blood was spun down at 7500 rpm for 10 min at 4 °C and the sera was collected and stored at −80 °C. The sera were then subjected to aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activity testing by following the manufacturer's guidelines (Abcam). Briefly, the sera were diluted 10x, and compared against a standard curve of pyruvate and glutamate for the ALT and AST assay, respectively. Fluorometric readings at 535 nm (excitation) and 587 nm (emission) and at 10 and 40 min were used to measure ALT activity while AST activity was measured using absorbance readings at 450 nm also at 10 and 40 min (Tecan plate reader).
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