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Xn 1000v

Manufactured by Sysmex
Sourced in Japan, Germany

The Sysmex XN-1000V is a compact and automated hematology analyzer designed for routine blood cell analysis. It provides reliable and accurate results for a wide range of clinical parameters, including red blood cells, white blood cells, and platelets. The XN-1000V is intended for use in clinical laboratories and healthcare settings.

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12 protocols using xn 1000v

1

Leukocyte Changes in Drug Discontinuation

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CBC was measured using a CBC analyzer (Sysmex, #XN-1000 V) to determine the changes in the number of leukocytes in the vehicle group subjected to the drug discontinuation regimen and the levels of CKD-506 and fingolimod in the blood of the vehicle groups subjected to the drug discontinuation and drug change regimens.
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2

Comprehensive Canine Biomarker Analysis

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Blood EDTA samples were used for complete blood cell count (CBC) with the haematology analyser XN-1000V (Sysmex Europe GmbH, Norderstedt, Germany), equipped with a veterinary software (Software of Automated hematology Analyzer for Animal XN-V series (Sysmex). All samples were analysed within 8 hours after blood collection. Blood plain tubes were centrifuged 3000xg for 10 minutes and serum samples were collected for biochemical analysis: routine biochemical pro le analysis were performed using an automated clinical chemistry analyser (Cobas C501; Roche Diagnostics International AG, Rotkreuz, Switzerland); folate and cobalamin (B12) immunoassay analysis were performed with automated Cobas e601 analyser (Roche Diagnostics). Serum canine C reactive protein (cCRP) concentration was determined via a commercially available turbidimetric immunoassay kit (Turbovet canine CRP, Acuvet Biotech,Zaragoza, Spain) applied to Cobas C501 analyser, following manufacturer instruction.
Faecal calprotectin was determined via a species-speci c ELISA kit (Canine Calprotectin CP, MyBioSource, San Diego, CA), following manufacturer instruction. Brie y, 10 mg of samples were homogenized in 100 µL of PBS and centrifuged for 20 minutes at 1500xg; supernatant was carefully collected and stored at -80°C until analysis. Faecal samples were then thawed and measured in a unique batch.
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3

Detailed Blood Sampling Protocol for Hematology

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Demographics for the 18 participants in the study are shown in S1 Table and in a schematic of the Schedule of Assessments. A total volume of 95.5 mL of blood was collected per donor and distributed into eight tubes (K2-EDTA, 10 mL lavender/H, #367525 BD Vacutainer) and four EDTA tubes (K2-EDTA, 3 mL lavender/H, #367838 BD Vacutainer) for cell differentials (CBC) at 5 time points: 3h (baseline), 6h, 24h, 48h & 72h, flow cytometry analysis (at 3, 24, 48 & 72h) and plasma collection (all time points), and in one 3.5 mL serum separation tube (Serum separator tubes, SST™ II advance, BD Vacutainer® ref 368498 (Becton Dickinson Sweden AB)) for serum collection (baseline (3h) only). The 3 mL EDTA tubes were transferred at ambient temperature to the Hematology unit, at Sahlgrenska University Hospital (Gothenburg, Sweden), for CBC analysis on the Abbott CELL-DYN Sapphire hematology analyzer. The eight 10 mL EDTA test tubes per donor were transferred at ambient temperature to the Bioscience department at AstraZeneca (Gothenburg) to be analyzed on the Siemens ADVIA 2120i, Beckman Coulter DxH900, and Sysmex XN-1000V hematology analyzers. Two 10 mL EDTA tubes from each donor were placed at four different temperatures: in the refrigerator (at 4°C), in a box on the bench (room temperature (RT) of 20°C), and in heating cabinets (at 30 and 37°C).
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4

Evaluating Bone Formation After EHP Treatment

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At the end of the 8 weeks after treatment with EHP, blood samples were collected from the ear vein, white blood cell (WBC) counting was detected by Automated Hematology Analyzer (Sysmex, XN-1000 V, Japan), and alkaline phosphatase (ALP) level was detected by using ELISA kit (Beyotime Biotechnology Co. Ltd., Shanghai, China). The rabbits were euthanized and tibia specimens were examined by micro computed tomography (micro-CT, SkyScan-1172, Bruker, Switzerland). The indexes such as bone volume/tissue volume ratio (BV/TV) and bone mineral density (BMD) were analyzed to evaluate bone formation [22 (link)].
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5

Comprehensive Canine Health Profiling

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Blood EDTA samples were used for complete blood cell count (CBC) with the hematology analyzer XN-1000 V (Sysmex Europe GmbH, Norderstedt, Germany), equipped with veterinary software (Software of Automated hematology Analyzer for Animal XN-V series (Sysmex). All samples were analyzed within 8 h after blood collection. Blood plain tubes were centrifuged 3000× g for 10 min, and serum samples were collected for biochemical analysis: routine biochemical profile analysis was performed using an automated clinical chemistry analyzer (Cobas C501; Roche Diagnostics International AG, Rotkreuz, Switzerland); folate and cobalamin (B12) immunoassay analysis was performed with an automated Cobas e601 analyzer (Roche Diagnostics). Serum canine C reactive protein (cCRP) concentration (mg/L) was determined via a commercially available turbidimetric immunoassay kit (Turbovet canine CRP, Acuvet Biotech, Zaragoza, Spain) applied to a Cobas C501 analyzer, following the manufacturer’s instructions. Fecal calprotectin was determined via a species-specific ELISA kit (Canine Calprotectin CP, MyBioSource, San Diego, CA, USA), following the manufacturer’s instructions. Briefly, 10 mg of samples were homogenized in 100 μL of PBS and centrifuged for 20 min at 1500× g; the supernatant was carefully collected and stored at −80 °C until analysis. Fecal samples were then thawed and measured in a unique batch.
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6

Determination of HIV-1 RNA Levels

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CRP was detected by immunoturbidimetric method through C-reactive protein kits (E023, Nanjing Jiancheng Bioengineering). White blood cell (WBC) were detected by automatic blood cell counter (XN-1000V, Sysmex). The patient's 4 ml venous blood was placed in EDTA anticoagulant tube to separate the plasma, and the HIV-1 Qualitative Test kit (Roche, Germany) was used for real-time fluorescence RT-qPCR analyzer (BIO-RAD, Germany) to determine the HIV-RNA load, set positive control and negative control, HIV-RNA copies were converted to geometric mean representation.
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7

Comprehensive Blood Analysis in Mice

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Peripheral blood samples were collected from mice eyes; complete blood count including Red Blood Cell (RBC), Hemoglobin (HGB), and Neutrophil (NEUT), Platelet (PLT), Reticulocyte (RET), White Blood Cell (WBC), Lymphocyte (LYM), immature reticulocyte fraction (IRF) were estimated using Sysmex XN-1000V automated hematology analyzer (Japan).
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8

Comparative Hematology Analyzer Evaluation

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We used the Abbott CELL-DYN Sapphire, Beckman Coulter DxH900, Siemens ADVIA 2120i, and the Sysmex XN-1000V hematology analyzers to count and compare cell differentials in whole blood. All samples (shaken/not shaken and stored at different temperatures) were measured simultaneously (within 10% time deviation) in the ADVIA, Beckman, and SYSMEX analyzers at AstraZeneca according to the manufacturers’ instructions. Blood from 12 donors (n = 6 with asthma and n = 6 healthy (n = 3 with/without atopy)) was analyzed using the Abbott CELL-DYN Sapphire at the Sahlgrenska University Hospital (non-shaken samples only, same temperatures and time windows). An overview of the technical details of each hematology analyzer is given in the supplementary description (reference to MAPSS Optical Cell Detection Technology (hematologyacademy.com), ADVIA® 2120i Hematology System (https://www.medicodistributors.in/siemens-advia-2120i), Evaluation of the New Beckmann Coulter Analyzer DxH 900 Compared to Sysmex XN20 [8 (link)], Performance evaluation of the new hematology analyzer Sysmex XN-series [9 (link)], and Spurious white blood cell count from a new automated Sysmex XN hematology analyzer [10 (link)]).
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9

BALF Cell Counts and Protein Levels

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Cell counts in BALF samples were analyzed by the multispecies hematology analyzer (Sysmex XN-1000 V, Japan). The protein concentrations of BALF were measured.
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10

Whole Blood and Biochemical Analysis

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In brief, the whole blood count was measured using XN-1000 V (Sysmex, Denmark), and the biochemical test was performed using 3100 (Hitachi, Japan), all procedures followed manual instructions and were operated by professional personnel.
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