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Serum Amyloid A POC Test Kit Immunoassay CFDA Approved

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Serum Amyloid A POC Test Kit Immunoassay CFDA Approved

Serum Amyloid A POC Test Kit Immunoassay CFDA Approved
Serum Amyloid A POC Test Kit Immunoassay CFDA Approved Serum Amyloid A POC Test Kit Immunoassay CFDA Approved Serum Amyloid A POC Test Kit Immunoassay CFDA Approved Serum Amyloid A POC Test Kit Immunoassay CFDA Approved

Large Image :  Serum Amyloid A POC Test Kit Immunoassay CFDA Approved

Product Details:
Place of Origin: China
Brand Name: Lumigenex
Certification: ISO13485, cFDA
Model Number: T2011-020, T2011-050
Payment & Shipping Terms:
Minimum Order Quantity: 1250 tests
Price: USD 3.0/ Test
Packaging Details: 20 tests/box, 50 tests/box
Delivery Time: 2-10 Days
Payment Terms: T/T, Western Union,Paypal
Supply Ability: 100,000 tests/day

Serum Amyloid A POC Test Kit Immunoassay CFDA Approved

Product Name: Serum Amyloid A (SAA) Test Kit (TRFIA) Function: Inflammation Marker
Technology: Time Resolved Fluorescence Immunochromatographic Assay Usage: In Vitro Diagnostic Reagent
Format: Strip, Cassette Specimen: Whole Blood, Plasma, Serum
Reading Time: 15 Min. Storing Temperature: 2℃-8℃
Shelf Life: 18 Months Compatible Equipment: Lumigenex TRFIA Analyzer LTRIC-600, LTRIC-1000
High Light:

SAA POC Test Kit Immunoassay


CFDA Approved Quantitative Detection Kit


CFDA Approved Quantitative Rapid Test Kit

TRFIA Platform Serum Amyloid A(SAA)POC Test Kit Immunoassay Medical Infection Disease Quantitative Rapid Test Kit

High sensitivity cFDA approved SAA Quantitative Detection Kit (TRFIA)


Intended Use

In vitro quantification of serum amyloid A in human serum, plasma, and whole blood is possible using this serum amyloid A detection kit (time-resolved fluorescence immunoassay).

Serum amyloid A (SAA) is an acute phase protein that may be used to help diagnose inflammation and evaluate acute phase response mechanisms. Its concentration in the blood may rapidly increase under inflammatory, infectious, and noninfectious conditions. SAA is associated with high-density lipoprotein (HDL), which regulates HDL metabolism during inflammation. SAA breakdown products may build up in many organs as amyloid A fibrils, which has a profound impact on chronic inflammatory diseases. In clinical laboratory diagnostics, cheiluminescence and colloidal gold immunochromatography are common approaches for detecting SAA.


This SAA Quantitative Detection Kit (TRFIA) uses time-resolved fluorescence immunochromatography to determine serum amyloid A levels in serum, plasma, and whole blood.

The blood sample and sample detection solution were combined and added to the reagent card. On the marker pad, the test material (SAA) was coupled with the mouse anti-human serum amyloid A monoclonal antibody nano-microsphere fluorescent probe to create a complex (i.e., the monoclonal antibody probe). Capillary action chromatography was used to detect a monoclonal antibody detection line comprising mouse anti-human serum amyloid A, which was then captured to create a double antibody sandwich complex (i.e. monoclonal antibody-monoclonal antibody-monoanti-nano-microsphere fluorescent probe). As a consequence, the concentration of SAA in the sample rises, and the double antibody sandwich accumulation on the detection line grows. The control line was chromatographed with the unreacted excess Mono-anti-nano-microspheres fluorescent probe. The intensity of the fluorescence on the detection line is proportional to the concentration of the item (SAA) in the sample, and the regression equation is formed and saved on the IC card.

The Time-Resolved Fluorescence Immunoanalyzer reads the regression equation data in the IC card, tests the fluorescence intensity on the detection line, and then replaces the fluorescence intensity with the regression equation for automatic calculation, that is, the concentration of the object (SAA) in the output sample.


Serum Amyloid A POC Test Kit Immunoassay CFDA Approved 0Serum Amyloid A POC Test Kit Immunoassay CFDA Approved 1



1. Advanced: quantitative chromatography using time-resolved fluorescence immunoassays.

2. Quantitative: quantification of SAA detection

3. Precision: highly associated with imported chemiluminescence reagent (r> 0.975).

4. High sensitivity: detection limit of 1.0 ng/mL is low.

5. Simple: easy to use, appropriate for bedside detection

6. Broadly applicable: outpatient laboratory, emergency laboratory, medical center, cardiology, intensive care unit, and so forth.




Product Name
SAA Quantitative Detection Kit
Brand Name
Time Resolved Fluorescence Immunechromatographic Assay
Whole Blood/S
Shelf time
18 months
1 test/pouch bag, 20tests/box,1000tests/case;




Serum Amyloid A POC Test Kit Immunoassay CFDA Approved 2Serum Amyloid A POC Test Kit Immunoassay CFDA Approved 3


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Hyperlipidemia Lipid Panel
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Tel: 86-13814877381

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