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WAKO

WAKO

Wako offers in vitro diagnostics products, including IVD test systems and reagents for clinical chemistry and research laboratories. The company’s product offering includes clinical diagnostic reagents, HCC biomarkers and research reagents.
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About WAKO

Wako offers in vitro diagnostics products, including IVD test systems and reagents for clinical chemistry and research laboratories. The company’s product offering includes clinical diagnostic reagents, HCC biomarkers and research reagents.

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Clinical Chemistry Control
Wako Control Serum

Wako Control Serum is an in vitro diagnostic (IVD) control material for common clinical chemistry parameters in human diagnostics: NEFA, D-BIL, T-BIL, HDL and LDL. The lyophilized serum based on human serum is suitable for use with both manual and automated analytical procedures to monitor the precision of laboratory use.
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Total Bilirubin IVD Test
Total Bilirubin L-Type Assay

Total Bilirubin L-Type Assay is an in vitro diagnostic (IVD) test for the quantitative determination of Total Bilirubin (T-BIL) in serum. It is a stable, liquid ready-to-use reagent based on a chemical oxidation method utilizing vanadate as an oxidizing agent (vanadate oxidation method).
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Clinical Diagnostic Reagent
NEFA-HR(2) Assay

NEFA-HR(2) Assay is an in vitro diagnostic (IVD) test for the quantitative determination of non-esterified fatty acids (NEFA) in serum. Based on the enzymatic method using 3-Methyl-N-Ethyl-N-(β-Hydroxyethyl)-Aniline (MEHA) as a violet color agent, it delivers accurate, precise, simple and fast results without interference from ascorbic acid and bilirubin.
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Clinical Laboratory

Clinical Chemistry Control
Wako Control Serum

Wako Control Serum is an in vitro diagnostic (IVD) control material for common clinical chemistry parameters in human diagnostics: NEFA, D-BIL, T-BIL, HDL and LDL. The lyophilized serum based on human serum is suitable for use with both manual and automated analytical procedures to monitor the precision of laboratory use.
More details

Total Bilirubin IVD Test
Total Bilirubin L-Type Assay

Total Bilirubin L-Type Assay is an in vitro diagnostic (IVD) test for the quantitative determination of Total Bilirubin (T-BIL) in serum. It is a stable, liquid ready-to-use reagent based on a chemical oxidation method utilizing vanadate as an oxidizing agent (vanadate oxidation method).
More details

Clinical Diagnostic Reagent
NEFA-HR(2) Assay

NEFA-HR(2) Assay is an in vitro diagnostic (IVD) test for the quantitative determination of non-esterified fatty acids (NEFA) in serum. Based on the enzymatic method using 3-Methyl-N-Ethyl-N-(β-Hydroxyethyl)-Aniline (MEHA) as a violet color agent, it delivers accurate, precise, simple and fast results without interference from ascorbic acid and bilirubin.
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In Vitro LDL-C Assay
L-Type LDL-C

The L-Type LDL-C is an in vitro assay for the quantitative determination of low density lipoprotein cholesterol (LDL-C) in serum and plasma. It is a homogeneous assay, which eliminates the preparatory steps or calculation, allowing for its application on automated analyzers.
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In Vitro HDL-C Assay
L-Type HDL-C

The L-Type HDL-C is an in vitro assay for the quantitative determination of high density lipoprotein cholesterol (HDL-C) in serum. It is a direct method consisting of convenient liquid type reagents and employs a specific antibody which allows the assay to be directly measured on automated analyzers.
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In Vitro Liposome Immunoassay
Autokit CH50

The Autokit CH50 is an in vitro liposome immunoassay (LIA) for the quantitative determination of total complement activity (CH50) in human serum using an automated procedure. It uses a homogeneous population of small-size liposomes (200nm), which gives stable dispersion and uses Glucose-6-phosphate dehydrogenase (G6PDH) as the entrapped enzyme that has optimal activity at a neutral pH.
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Immunoanalyzer
μTASWako i30

The μTASWako i30 is a micro-fluidic-based clinical immunoanalyzer for in vitro diagnostic use which minimizes instrument hands-on time while maximizing efficiency through integration and automation of clinical laboratory processes. It takes nine minutes to first result and two minutes per subsequent result, has a throughput of 25 results per hour, and can measure up to six analytes per sample.
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Immunological Test System
μTASWako DCP

The μTASWako DCP immunological test system is an in vitro device consisting of reagents used with the μTASWako i30 immunoanalyzer to quantitatively measure, by immunochemical techniques, des-gamma-carboxyprothrombin (DCP) in human serum. It is ideal for use as an aid in the risk assessment of patients with chronic liver disease for development of hepatocellular carcinoma (HCC) in conjunction with other laboratory findings, imaging studies, and clinical assessment.
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Immunological Test System
μTASWako AFP-L3

The μTASWako AFP-L3 immunological test system is an in vitro device that consists of reagents used with the μTASWako i30 Immunoanalyzer to quantitatively measure, by immunochemical techniques, AFP-L3% in human serum. It is ideal for use as an aid in the risk assessment of patients with chronic liver disease for development of hepatocellular carcinoma (HCC) in conjunction with other laboratory findings, imaging studies and clinical assessment.
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