Serum Amyloid A (SAA) Test Kit (FIA) 00022C

Product catalog summary

Overview: Serum Amyloid A (SAA) is a critical biomarker for detecting tissue injury and inflammation. It is classified as an acute phase protein due to its rapid increase in response to inflammation or tissue damage, with levels potentially rising up to 1000-fold.

Product Specifications:

Sample Types: Whole Blood (WB), Serum (S), Plasma (P)
Sample Volume: 5 μL
Assay Time: 5 minutes
Working Range: 5-300 mg/L
Performance: Coefficient of Variation (CV) ≤ 15%
Storage Conditions: 2-30°C
Shelf Life: 18 months

Ordering Information: The Serum Amyloid A (SAA) Test Kit is available in packs of 25 tests per box, with 20 boxes per carton. Compatible with KS-001 and KS-002 analyzers.

Analyzer Specifications:

KS-001: Single-channel, 120 tests/hour, 7” LCD touch screen, built-in thermal printer, dimensions 265x212x128 mm, weight 2.5 kg.
KS-002: 12-channel, up to 120 tests/hour, 8” LCD screen with VGA interface, built-in thermal printer, dimensions 490x328x336 mm, weight 16 kg.

Technical Strengths:

Semi-Liquid Phase Reaction enhances sensitivity and accuracy by allowing more complete antigen-antibody binding.
Red Nanofluorescent Microsphere Technology provides stability and reduces interference from endogenous substances.

Clinical Reference and Certification: The SAA test is certified by CE and NMPA, with a clinical reference range of less than 10 mg/L.

Additional Test Parameters: The document also lists various other tests with their respective sample types, volumes, assay times, working ranges, clinical references, shelf lives, and certifications, including tests for cardiac markers, diabetes, hormones, infections, and other conditions.

Catalog excerpts

Serum Amyloid A (SAA) Test Kit (FIA) 00022C-1

Serum amyloid A (SAA) is an early and sensitive blood biomarker for tissue injury and inflammation and has been indicated in many inflammatory diseases. The level of SAA circulating in the blood is known to increase dramatically in response to tissue damage or inflammation, classifying it as an acute phase protein. Circulating SAA concentrations may increase up to 1000-fold following inflammation, infection, tissue injury and cell necrosis and decline rapidly following recovery. Test cassette Extraction buffer Beijing O&D Biotech Co., Ltd. Web: www.odbio.com Contact: Grace Zhang, [email protected]; Jason Du, [email protected] ADD: West, Floor 4, Building 1, No.1, Shunqiang Road, Renhe Town, Shunyi District, Beijing, China

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Serum Amyloid A (SAA) Test Kit (FIA) 00022C-2

Specification Sample type Sample vol. Assay time Working range Performance Storage Shelf Life Ordering Information Item Serum Amyloid A (SAA) Test Kit Packing 25 tests/box; 20 boxes/ctn

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Serum Amyloid A (SAA) Test Kit (FIA) 00022C-3

Compatible Instruments Specifications Item KS-001 Dry Fluorescent Immunoassay Analyzer KS-002 Dry Fluorescent Immunoassay Analyzer Catalogue Number Testing Modes Auto-test/Queuing/Instant test Automatic testing Testing Speed 120 T/h under the Queuing Mode 8" LCD screen. The instrument can be connected to a monitor by VGA interface. Built-in thermal printer Built-in thermal printer

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Serum Amyloid A (SAA) Test Kit (FIA) 00022C-4

Technical Strength 1. Semi-Liquid Phase Reaction Half of the immune reaction is done in the liquid phase, which effectively improves the sensitivity and accuracy of the product. In the sample, the antigen binds more fully to the fluorescently labeled antibody. The release of fluorescent microspheres on the NC membrane is more uniform. Test results of whole blood samples have better repeatability. 2. Red Nanofluorescent Technology a. Comparing with ordinary fluorescein 1) FITC (fluorescein isothiocyanate) and other fluorescent substances are light sensitive and thus easily quenched. Their fluorescence...

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