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Abk pentra 400

Manufactured by Horiba
Sourced in France

The ABK Pentra 400 is a clinical chemistry analyzer designed for routine testing in medical laboratories. It provides automated analysis of a wide range of clinical chemistry parameters from patient samples. The instrument features advanced technology for accurate and reliable results.

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2 protocols using abk pentra 400

1

Blood Collection and Analysis Protocol

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Four [4 ] ml of blood was drawn by venipuncture and placed into heparinized vacutainer tubes (Becton Dickinson, Franklin lakes, NJ USA) by the study doctor or nurse. Complete blood counts were analyzed using a coulter counter at the Uganda cancer institute laboratory. HIV serological testing was done at MNU side lab using rapid tests (Determine HIV-1/2 [Abbot Laboratories USA], and positive samples were confirmed with HIV-1/2 Stat-Pak Dipstick Assay kit. HIV DNA/PCR test was done at the hospital’s HIV clinic for all children aged below 18 months with a positive serology test. Plasma was obtained by centrifuging at 1300-2200G for 10 min, then stored at − 80 °C at Immunology Laboratory, Mulago Hospital until shipped on dry ice to the Department of Nutrition, Exercise and Sports, University of Copenhagen, Denmark. Plasma C-reactive Protein (CRP) was measured by high sensitive kit on an ABK Pentra 400 (Horiba, Montpellier, France).
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2

Quantifying Plasma Citrulline and CRP in HIV Patients

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Four milliliters of venous blood was collected into EDTA-treated Vacutainer tubes (Becton Dickinson; Franklin lakes, NJ USA). Samples for complete blood counts were analyzed using a Coulter counter at the Uganda Cancer Institute laboratory. HIV sero-status was assessed at the MNU side laboratory using Determine HIV-1/2 (Abbot Laboratories USA) rapid tests and HIV-1/2 Stat-Pak Dipstick Assay kit for children aged ≥18 mo. For those <18 mo of age, their HIV status was confirmed using an HIV DNA/polymerase chain reaction (PCR) test done at Baylor HIV clinic. Plasma was obtained by centrifuging at 1300–2200 g at ambient temperature for 10 min, and stored at −80°C prior to shipment on dry ice to the University of Copenhagen, Denmark. Plasma C-reactive protein (CRP) was analyzed by the high-sensitivity kit on an ABK Pentra 400 (Horiba; Montpellier, France). Detection of plasma citrulline has been described in detail elsewhere (40 (link)). Briefly, the LC-MS method (41 ) was used. Samples were processed with Sirocco protein precipitation plate (Waters) and separated on an ACQUITY UPLC HSS T3 Column (Waters) using an ultra-performance LC in tandem with triple quadrupole detector MS. l-Citrulline-4,4,5,5-d4 (Sigma-Aldrich) was used as an internal standard. Quantification of citrulline was carried out using QuanLynx (Waters).
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