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2 in 1 (CEA/AFP) Rapid Quantitative Test
Biotime
ProductNewReviewed

2 in 1 (CEA/AFP) Rapid Quantitative Test

The 2 in 1 (CEA/AFP) Rapid Quantitative Test provides simultaneous detection of Carcinoembryonic Antigen (CEA) and Alpha-fetoprotein (AFP) in human serum or plasma. This dual-marker fluorescent immunoassay supports liver cancer diagnosis and enhances

Minimum Order1 Carton
Warranty1 Year
Regulatory ApprovalsWHO Prequalified, CFDA/NMPA, ISO 13485 Certified, CE Marked, FDA Approved
Country of OriginFlag of ChinaChina
BrandBiotime

Product Rating

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Description

The Biotime 2 in 1 (CEA/AFP) Rapid Quantitative Test is a fluorescence-based immunoassay designed to measure CEA and AFP concentrations in serum or plasma samples within 10 minutes. Both markers are clinically significant for evaluating and diagnosing primary liver cancer, metastatic liver disease, and other malignancies.

AFP (Alpha-fetoprotein) is a major plasma protein produced by the fetal liver and yolk sac during development. Its levels decrease rapidly after birth, remaining low in healthy adults. Elevated AFP may indicate hepatocellular carcinoma, germ cell tumors, or metastatic liver involvement.

CEA (Carcinoembryonic Antigen), a glycoprotein involved in cell adhesion, is normally produced during fetal development but is nearly absent in healthy adults. Elevated CEA levels are associated with colorectal, pancreatic, gastric, and lung cancers, making it an essential biomarker for tumor monitoring and recurrence evaluation.

By combining these two clinically relevant markers, the Biotime 2 in 1 (CEA/AFP) test delivers comprehensive diagnostic value, reducing testing time while maintaining high analytical sensitivity and accuracy.

Key Features

  • Simultaneous detection of CEA and AFP in a single test cartridge
  • Rapid results within 10 minutes for efficient clinical decision-making
  • High sensitivity and specificity for tumor marker screening
  • Avoids hook effect, ensuring accurate quantification
  • Dual-marker panel improves liver cancer diagnostic accuracy
  • Convenient and reliable for oncology and gastroenterology applications

Technical Specifications

  • Specimen Type: Serum / Plasma
  • Specimen Volume: 20μL
  • Sample Capacity: 80μL
  • Reaction Time: 10 minutes
  • Detection Range: Refer to individual item (CEA and AFP)
  • Assay Method: Fluorescence Immunoassay
  • Measurement Mode: Quantitative
  • Storage Temperature: 2–30°C
  • Shelf Life: 18 months
  • Analyzer Compatibility: Biotime Fluorescence Immunoassay Analyzer

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Standard Accessories

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Package Contents

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Related Searches

CEA Test AFP Test Dual Marker Test Liver Cancer Test Tumor Marker Test Quantitative Rapid Test Oncology Screening Kit Fluorescence Immunoassay POCT
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Xiamen Biotime Biotechnology Co., Ltd Logo

Xiamen Biotime Biotechnology Co., Ltd

China FlagNo. 1565 Xiang’an North Road, Xiamen, Fujian, China

Reviewed manufacturer

Member Since

18 Oct 2025

Last Active

04 Aug 2026

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