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Sterile vacutainer tubes

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Sterile vacutainer tubes are laboratory specimen collection devices used to draw and contain blood samples. They are designed to maintain the sterility and integrity of the collected sample for subsequent analysis or testing.

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4 protocols using sterile vacutainer tubes

1

Comprehensive Evaluation of Adolescent Diabetes

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All included adolescents were subjected to detailed medical history with special emphasis on disease duration, insulin daily dose (U/kg/day), exercise and the presence of clinically significant hypoglycemic episodes “i.e. glucose value of < 3.0 mmol/l (54 mg/dl)/week” [14 (link)]. The socioeconomic status was assessed using the validated Arabic socioeconomic status scale for health research in Egypt. It is a scale with 7 domains with a total score of 84. According to the scale the socioeconomic level is classified into very low, low, middle and high levels depending on the quartiles of the score calculated [15 (link)].
Thorough clinical examination was done laying stress on anthropometric measures and body mass index (BMI) measured as kg/m2 with calculation of z score [16 ]. Peripheral blood samples were collected on potassium-ethylene diamine tetra-acetic acid (K2-EDTA) in sterile vacutainer tubes (final concentration of 1.5 mg/ml) (Beckton Dickinson, Franklin Lakes, NJ, USA) for assessment of HbA1C.
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2

Venous Blood Sampling for Epigenetic Analysis

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Venous blood samples (15 mL) were taken from the antecubital vein using sterile vacutainer tubes (Becton-Dickinson, Oxford, UK) before and immediately after experimental exercise sessions. The peripheral blood was used to acquire the PBMCs for epigenetic analysis and plasma for oxidative stress marker measurements. The samples were aliquoted and frozen at –20°C.
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3

Canine Serum Biomarker Measurement

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To minimize the influence of feeding, all dogs were fasted for 12 hr before the collection of blood samples. Whole blood was withdrawn from either the cephalic
or jugular veins for determination of serum levels of Cys-C and SDMA. Blood samples were drawn directly into sterile vacutainer® tubes (BD, Franklin
Lakes, NJ, U.S.A.) and then centrifuged at 1,500 × g for 10 min at 4°C. The supernatants were stored at −80°C or dry ice for shipping or
testing. Serum Cys-C levels were measured using a commercial ELISA based kit (Dog Cystatin C ELISA kit, MyBioSourse, San Diego, CA, U.S.A.), according to the
manufacturer’s recommendation. The Cys-C ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-Cys-C antibody and a
Cys-C-HRP conjugate. Prior to a study, the test kit and method were completely validated for use with dog serum. We also tested serial dilutions of the samples
in duplicate. N-terminal pro brain natriuretic peptide (NT-proBNP) and SDMA concentrations were determined by reference laboratory (IDEXX Laboratories,
Westbrook, ME, U.S.A.). Concentrations of serum urea nitrogen (UN) and CRE were determined with an automated biochemistry analyzer (VetScan VS2, Abaxis, Union
city, CA, U.S.A.).
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4

Plasma and PBMC Extraction from Venous Blood

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40 ml venous blood was collected in EDTA containing sterile vacutainer tubes (BD Biosciences) at the visit. Plasma collection was performed by centrifuging the blood at 400 g for 10 min and plasma was collected and further centrifuged at 1000 g for 15 min to remove the platelets. Plasma was stored at −80 °C until further use. Peripheral blood mononuclear cells (PBMC) were collected from the whole blood by density gradient method and cells were cryopreserved in liquid N2. All the laboratory procedures used sterile endotoxin free tubes.
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