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Xn 1000 automated hematology analyzer

Manufactured by Sysmex
Sourced in Japan

The XN-1000 Automated Hematology Analyzer is a diagnostic instrument designed to perform complete blood count (CBC) and related tests. It utilizes advanced technology to automate the analysis of blood samples, providing accurate and reliable results.

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7 protocols using xn 1000 automated hematology analyzer

1

Blood Biomarker Profiling in Clinical Setting

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Blood samples were obtained from the antecubital vein after the first admission and following a 12hour fasting. Biochemical analyses were performed with an Architect Ci 8200 (Abbott Laboratories, Lake Bluff, IL, USA), Full blood counts were performed with an XN-1000 Automated Hematology Analyzer (Sysmex, Tokyo, Japan), and biochemical analyses were performed with an Architect Ci8200 (Abbott Laboratories, Lake Bluff, IL, USA). Fasting blood glucose, creatinine, albumin, total protein, blood urea nitrogen, total cholesterol, low-density lipoprotein, very low-density lipoprotein, high-density lipoprotein, and triglycerides were measured during the biochemical analysis.
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2

Comprehensive Blood Panel Analysis

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Using sterile venipuncture, six milliliters of fresh venous blood were taken. Two milliliters of blood were immediately transferred to an EDTA vacutainer tube for the total RNA extraction and complete blood count (CBC) via the Sysmex XN-1000 Automated Hematology Analyzer, Kobe, Japan; 2 mL was transferred to a sodium citrate vacutainer tube for the D-dimer test by the Fully Automated Coagulation System, Diagnostic Stago, France. The remaining 2 mL was transferred to a plain tube and centrifuged at 4000 rpm for 20 min. The serum was then refrigerated at −20 °C until the measurements of serum ferritin using the Abbott chemiluminescence immunoassay, North Chicago, IL, USA; of the C-reactive protein (CRP) using the nephelometric method by Mispa-i2, and of interleukin 6 (IL-6) using the enzyme-linked immunosorbent assay (ELISA) human kits.
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3

Comprehensive Blood Component Analysis

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Venous peripheral blood (whole blood) samples were collected in ethylenediaminetetraacetic acid (EDTA) tubes which is usually used for blood count measurement for peripheral blood separately from the PRP preparation kit, and part of the PRP used for treatment was used for hematological analysis. Peripheral blood and PRP samples were analyzed using an XN-1000 automated hematology analyzer (Sysmex, Kobe, Japan) according to the manufacturer's recommendations. The concentrations of erythrocytes, neutrophils, lymphocytes, monocytes, platelets, and IPF were measured from 300 μL of peripheral blood and PRP.
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4

Comprehensive Blood Biomarker Assessment

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After the first admission and following a 12-hour fast, blood samples were obtained from the antecubital vein. Full blood counts were analyzed within 45 minutes of obtaining blood sample. The venous blood samples obtained for biochemical analysis were centrifuged at 3000 rpm. They were then stored at −80°C until analysis. Biochemical analyses were performed with an Architect Ci8200 (Abbott Laboratories, Lake Bluff, IL, USA), and full blood counts were performed with an XN-1000 Automated Hematology Analyzer (Sysmex, Tokyo, Japan). All analyses were performed by a laboratory technician who was blinded to the patient data. The following parameters were measured during the biochemical analysis: fasting blood glucose, creatinine, albumin, total protein, sodium, potassium, blood urea nitrogen, aspartate transaminase, alanine transaminase, uric acid, calcium, C-reactive protein (CRP), thyroid-stimulating hormone, total cholesterol, low-density lipoprotein, very-low-density lipoprotein, high-density lipoprotein, and triglycerides. The full blood count included measurement of the red blood cell count, hemoglobin, hematocrit, red cell distribution width (RDW), platelet count, platelet distribution width, WBC count, neutrophil count, and lymphocyte count. The ratio of the neutrophil count over the lymphocyte count was recorded as the NLR.
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5

Gastric Biomarkers and Metabolic Factors

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The demographic characteristics and clinical variables were collected from the admission record including age, sex, body mass index (BMI), tobacco use and alcohol consumption, systolic blood pressure, diastolic blood pressure, leucocyte count, neutrophil count, lymphocyte count, monocyte count, high-sensitivity C-reactive protein (hs-CRP), blood urea nitrogen (BUN), uric acid (UA), creatinine (Crea), cystatin C (Cysc), total triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), homocysteine (Hcy), and medication history. The BMI was computed from measurements of height and weight (kg/m 2 ). Leucocyte count, neutrophil count, lymphocyte count, and monocyte count were measured by the XN-1000 Automated Hematology Analyzer (Sysmex, Japan). The concentration of hs-CRP, BUN, UA, Crea, CysC, TG, TC, HDL-C, LDL-C, and Hcy were measured by the AU5400 Automated Biochemical Analyzer (Olympus, Japan). Serum PG levels were measured by the i2000 using a chemiluminescence immune assay (Abbott, USA), using the manufacturers' reagents, calibrators, and settings. Levels of serum PGI and PGR were categorized according to commonly used cut-off values in gastric diseases [10] , 30 or 70 ng/mL for PGI, and 3 for PGR. PGII lacked of widely-accepted cut-off and was divided into quartiles.
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6

Hematological and Coagulation Profile Analysis

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Red blood cell, white blood cell, and platelet counts were measured by flow
cytometry using Sysmex XN-1000 Automated Hematology Analyzer (Sysmex Corp,
Kobe, Japan). C-reactive protein (CRP), fibrinogen, activated partial
thromboplastin time (APTT), PT, and d-dimer were measured using the
following commercial kits: CRP-Latex X2 (Denka Seiken Co, Ltd, Niigata,
Japan), Thrombocheck Fib(L) (MBL Co, Ltd, Ina, Japan), Thrombocheck APTT-SLA
(Sysmex Corp), Thromborel S (Sysmex Corp), and Hexamate D-dimer (MBL Co,
Ltd), respectively.
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7

Multimodal Biomarker Assessment Protocol

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Mispa-i2 was used to calculate CRP using the nephelometric method (Agape Diagnostics, Switzerland). The Architect plus i1000SR immunoassay analyzer was used to measure serum ferritin using a chemoilumincence immunoassay (Abbott, Illinois, USA). The stago -STA Compact Max Analyzer, Fully Automated Coagulation System - was used to measure the D-dimer (Diagnostic Stago, France).
The Sysmex XN-1000 Automated Hematology Analyzer was used to measure WBCs and lymphocytes (Sysmex Corporation, Kobe, Japan). Quantikine, Canada, USA, provided enzyme-linked immunosorbent assay (ELISA) human kits for measuring serum IL-6 levels.
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