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Coulter hmx al hematology analyzer

Manufactured by Beckman Coulter
Sourced in United Kingdom

The Coulter HmX AL Hematology Analyzer is a laboratory instrument designed for the automated analysis of various blood parameters. The core function of this analyzer is to provide accurate and reliable measurements of red blood cells, white blood cells, and platelets in a patient's blood sample.

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2 protocols using coulter hmx al hematology analyzer

1

Smoking Impacts on Blood Cell Profiles

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253 individual study participants consisting of 172 smokers and 81 nonsmokers enrolled between 1993 and 1995 as healthy volunteers from the general public in Durham and Chapel Hill, North Carolina. These subjects were part of a community-based sample comprised of 294 healthy unrelated blacks and whites; collection and processing have been described in several studies [3 ,4 (link),52 (link)]. An independent group of black and white females (20 smokers and 14 nonsmokers) was recruited at the NIEHS Clinical Research Unit (protocol 10-E-0063) between March 2013 and January 2015 from the Raleigh, Durham and Chapel Hill, NC area. All nonsmokers were self-reported as not having smoked >100 cigarettes in their lifetime. Smokers reported their average daily cigarette consumption for the past 3 months. Age and smoking history of all subjects are given in Tables 1 and 2 as average and range. Peripheral blood monocytes, lymphocytes, eosinophils, basophils and neutrophils were counted by an automated cell counter, Coulter HmX AL Hematology Analyzer (Beckman Coulter, UK) by the Hematological Laboratory at NIEHS. Serum nicotine/cotinine levels were measured by HPLC-MS (Quest, Inc). More details for all methods are provided in the Supporting files.
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2

Measuring Total White Blood Cells and CRP

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Total white blood cell count (WBC) was measured in fasting whole blood samples using an automated cell counter, Coulter HmX AL Hematology Analyzer (Beckman Coulter, High Wycombe, England, UK). Level of C-reactive protein (CRP) was measured in plasma from fasting blood samples using reagents from Roche Diagnostics (Mannheim, Germany) on a Hitachi 912 analyzer (Hitachi Ltd., Tokyo, Japan) according to the manufacturer’s instructions. Both within- and between-assay quality control procedures were used and the coefficient of variation of the method was 1.3% to 3.4%, respectively, through the preriod of data collection. All participants in this study had detectable CRP levels.
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