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Cobas 6000 integra system c 501

Manufactured by Roche
Sourced in Germany

The COBAS 6000 INTEGRA system c 501 is a clinical chemistry analyzer designed for in vitro diagnostic use. It is capable of performing a variety of clinical chemistry tests on patient samples. The core function of the system is to analyze and provide test results for clinical chemistry parameters.

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4 protocols using cobas 6000 integra system c 501

1

C-Reactive Protein and Leukocyte Quantification

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After the sample collection, the quantitative determination of C-reactive protein in human serum and plasma (the normal value is less than 6 mg/L) was measured in lithium heparin SARSTEDT Monovette 4.7 mL (orange top) using a standard immunoturbidimetric assay on the COBAS 6000 INTEGRA system c 501 (Roche Diagnostics Ltd, Mannheim, Germany). The determination of the leukocyte count (normal range 4000–10,000/μL) in the blood was generally carried out as a routine part of blood counts after collection in EDTA Monovette 2.7 mL by flow cytometry using the Sysmex XE 2100 hematology analyzer (Sysmex Germany Ltd, Norderstedt, Germany).
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2

Quantitative CRP and Leukocyte Analysis

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After the sample collection, the quantitative determination of C-reactive protein (CRP) in the human serum and plasma (the normal value is less than 6 mg/L) was measured in lithium heparin SARSTEDT Monovette® 4.7 ml (orange top) using a standard immunoturbidimetric assay on the COBAS® 6000 INTEGRA system c 501 (Roche Diagnostics Ltd, Mannheim, Germany). The determination of the leukocyte count (normal range 4000–10,000/μL) in the blood was generally carried out as a routine part of blood counts after collection in EDTA Monovette® 2.7 mL by flow cytometry using the Sysmex® XE 2100 hematology analyzer (Sysmex Germany Ltd, Norderstedt, Germany). CRP and leukocyte counts were compared between all patients in the study group.
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3

Quantification of CRP and Leukocyte Count

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After the sample collection, the quantitative determination of C-reactive protein (CRP) in human serum and plasma (the normal value is less than 6 mg/L) was measured in lithium heparin SARSTEDT Monovette 4.7 mL (orange top) using a standard immunoturbidimetric assay on the COBAS 6000 INTEGRA system c 501 (Roche Diagnostics Ltd, Mannheim, Germany). The determination of the leukocyte count (normal range 4000–10,000/μL) in the blood was generally carried out as a routine part of blood counts after collection in EDTA Monovette 2.7 mL by flow cytometry using the Sysmex XE 2100 hematology analyzer (Sysmex Germany Ltd, Norderstedt, Germany).
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4

Quantifying Serum CRP and Leukocytes

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The amounts of C-reactive protein (CRP) in human serum (the normal value is less than 6 mg/L) was measured in lithium heparin SARSTEDT Monovette® 4.7 ml (orange top) using a standard immunoturbidimetric assay on the COBAS® 6000 INTEGRA system c 501 (Roche Diagnostics Ltd, Mannheim, Germany). Leukocyte counts (normal range 4,000 – 10,000/μL) in the blood were generally measured as a routine part of the blood counts after blood collection in EDTA Monovette® (2.7 mL) by flow cytometry using the Sysmex® XE 2100 hematology analyzer (Sysmex Germany Ltd, Norderstedt, Germany).
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