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CA19-9 Antibody (Detection-FIA/CLIA)

Shenzhen, Guangdong, China

Humanized antibody for CA19-9 detection in FIA/CLIA applications. Used as a gastrointestinal tract-associated tumor marker with high sensitivity and good specificity for pancreatic cancer diagnosis and monitoring.

Manufactured by

Shenzhen, Guangdong, China

HeavyBio Inc. is a young expert in IVD raw materials for cardiac markers, tumor markers, inflammatory markers, neuroendocrine and infectious diseases, which has been committed to becoming the world's leading IVD reagent supplier since 2017. Based in Shenzhen, China, the company develops, manufactures and commercializes high-quality monoclonal antibodies, recombinant antibodies, antigens, etc., which are widely used in ELISA, CLIA, latex and rapid test platforms. Innovation and quality are our top priorities, market and customer orientation are our constant endeavors. HeavyBio Inc. has been at the forefront of fighting the Covid-19 pandemic since 2020, thanks to a professional team of more than 60% R D and technical service experts, which has earned a good reputation in the IVD field in China. HeavyBio Inc. is your trusted Chinese IVD solution provider and raw material specialist!

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CA19-9 Test Kit (CLIA)

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Tumor marker assay kit for CA19-9 detection using chemiluminescence immunoassay. Analytical sensitivity of 1.50 U/mL with linearity from 1.50 to 1000 U/mL.

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BiosPacific · United States

High-quality antibodies for CA19-9 cancer marker detection and immunoassay development. Essential for pancreatic and gastrointestinal cancer diagnostics.

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Anbio Biotechnology Limited · Germany

Immunoassay for carbohydrate antigen 19-9 measurement in clinical specimens. Supports pancreatic and biliary cancer monitoring.

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Boditech Med Inc. · South Korea

A diagnostic test reagent that supports the diagnosis of pancreatic cancer.

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CA19-9 Test

Medix Biochemica Oy AB · Finland

A diagnostic test for measuring Cancer Antigen 19-9 (CA19-9) levels in blood samples. This test is used in clinical laboratories for cancer screening and monitoring, particularly for gastrointestinal cancers.

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CA 19-9

VEDALAB SAS · France

Immunochromatographic rapid test for the quantitative determination of Cancer Antigen 19-9 (CA 19-9) in whole blood, serum or plasma. Measuring range: 30-1000 U/mL. Reading time: 15 minutes.

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Carbohydrate Antigen 19-9 (CA19-9) Test Kit

Nanjing Poclight Biotechnology Co.,Ltd. · China

An in vitro quantitative test kit using homogeneous chemiluminescence immunoassay for determination of Carbohydrate Antigen 19-9 in human serum and plasma. The test is used as an aid in the diagnosis of pancreatic cancer. For professional and laboratory use only, with 18 months shelf life and storage at 2-30°C without cold chain requirement.

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CA 19-9 Quantitative Rapid Test

VEDALAB SAS · France

Immunochromatographic rapid test for the quantitative determination of Cancer Antigen 19-9 (CA 19-9) in whole blood, serum or plasma. Measuring range: 30–1000 U/mL. Reading time: 15 minutes.

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Tumor markers

Institute of Isotopes Co. Ltd. · Hungary

CA19-9 is a tumour associated mucin-type high molecular weight glycoprotein antigen circulating in the blood and can be found in tissues. This test is useful in monitoring patients with confirmed pancreatic cancer whose CA19-9 levels are above the cut off at the time of the diagnosis. Patients negative for the Lewis blood group antigen have no CA 19-9 in their blood even in the presence of malignant disease.

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CanAg CA19-9 EIA

Fujirebio Diagnostics,Inc. · China

An in vitro diagnostic test kit for the detection of cancer antigen 19-9 (CA19-9), a tumor marker. The product is CE certified and complies with European in vitro diagnostic product directive 98/79/EC. It is manufactured by ISO13485 certified facilities in Gothenburg, Sweden and Malvern, Pennsylvania, USA.

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Tumor Marker

Healgen Scientific LLC · United States

CLIA-waived rapid immunofluorescence assay (FIA) test kit for qualitative detection of fentanyl in oral fluid samples. Enables quick screening in clinical and point-of-care settings with 510(k) clearance for reliable drug presence identification.

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