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Bc 6000

Manufactured by Mindray
Sourced in China

The BC-6000 is a hematology analyzer that provides complete blood count (CBC) and 5-part differential analysis. It utilizes advanced technology to deliver accurate and reliable results. The BC-6000 is designed for use in clinical laboratories and healthcare settings.

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Lab products found in correlation

4 protocols using bc 6000

1

Erythrocyte Agglutination Detection

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The following reagents were used: PBS buffer; 0.9% and 1.8% normal saline; 50% human erythrocytes; erythrocyte fragments; serum; the 200 U hemolysin (anti‐human O‐erythrocyte antibody); anti‐A and anti‐B blood grouping reagents. The reference preparation method for the corresponding reagent can be found in Supporting Information. The main analyzing instrument was a Mindray BC‐6000 auto hematology analyzer. When agglutination, count of free erythrocyte shoud be decrease; thus, the results were indicated by the count of erythrocyte or the mean hemoglobin concentration of erythrocytes (MCHC), MCHC= hemoglobin content/hematocrit (MCHC = Hb/Hct, g/L).
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2

Hematology and CRP Analysis Protocol

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Hematology analysis was performed using Mindray BC-6000 according to the standard operating procedure of the clinical laboratory in Shanghai East Hospital (south Branch). In brief, EDTA-K2 anti-coagulated whole blood was collected and hematology analysis was automatically performed within 30 minutes of collection. After hematology analysis, the above sample was used to measure the level of CRP (C-reactive protein) by Ottoman automatic real-time detection analyzer (UPPER Biotech Pharma CO., LTD, Shanghai, China).
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3

Comprehensive Blood Cell Analysis

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The complete blood count (CBC) determinations were performed using a state-of-the-art hematology analyzer, namely, the Mindray bc 6000. This analyzer has been well-established for its precision and accuracy in providing comprehensive blood cell counts and related parameters. The CBC measurements encompassed a range of parameters, including but not limited to red blood cell count (RBC), white blood cell count (WBC), hemoglobin concentration (HGB), hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), neutrophil count, lymphocyte count, eosinophil count, basophil count, monocytes count, platelet count (PLT), mean platelet volume (MPV), platelet distribution width (PDW), C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR). The analytical methodology, grounded in impedance principles, facilitated the extraction of the aforementioned measurements.
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4

Prognostic Indicators in SSNHL

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Laboratory blood tests of all patients were performed on the first day of admission, before initiating any treatment. Complete blood count measurements were performed using an automated blood cell counter (Mindray BC-6000, Shenzhen, China). Serum albumin levels were detected using automatic photometry commercial kits (Abbott C8000i, Abbott Park, IL). Serum CRP levels were detected using the nephelometric method (AU5800 System; Beckman Coulter Inc, Brea, CA) and serum fibrinogen levels were detected by Clauss method using a BCS Analyzer (Multifibren U; Siemens Healthcare, Erlangen, Germany). We retrospectively recorded the pre-treatment fibrinogen, CRP, WBC, hemoglobin, neutrophil, lymphocyte, platelet, and albumin levels of the patients and calculated FAR, CAR, NLR and PLR of the groups.
First, the comparisons of FAR, CAR, NLR, PLR, WBC and hemoglobin were performed among the groups. Then, the most significant indicator parameters of poor prognosis (non-recovery) in patients with SSNHL were statistically investigated.
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