SAA Serum Amyloid A Inflammation Test Kit 0.5-100.0mg/L Range

Inflammation Test with SAA (Serum Amyloid A) Assay Kit

Intended use:

In vitro quantitative determination of the concentration of serum amyloid A in human serum, human plasma, and human whole blood samples.

Summary:

SAA is a human acute phase protein, which is a normal component present at low levels in the blood. It rises quickly when the human body has bacterial or viral infectious inflammation, active disease, or large-scale tissue damage. In the acute phase of inflammation or infection ( 48h～72h) can increase rapidly, and decrease rapidly during the recovery period of the disease. Studies have shown that elevated serum SAA can be detected in diseases such as bacteria, fungi, viral infections, atherosclerosis, cardiovascular disease, and acute transplant rejection. Similar to C-reactive protein, SAA helps diagnose inflammation and evaluate its therapeutic effects. However, in some diseases, such as viral infections, cardiovascular diseases, transplant rejection, etc., SAA can be more sensitive than C-reactive protein, and can be Clinical diagnosis provides better reference value. Combined detection of C-reactive protein and SAA can improve the sensitivity of the diagnosis of infection. Commonly used detection methods include immunoturbidimetric method, enzyme-linked immunosorbent assay, immunofluorescence chromatography, chemiluminescence method, etc.

Storage and stability:

The test card and buffer can be stored at 2℃～30℃ for 24 months, and the buffer solution can be stored at 2℃～30℃ for 2h after opening the bottle. The aluminum foil bag of the test card should be used within 2 hours after it is opened. Transportation and storage should be carried out at 2℃～30℃.

Applicable instrument:

The models produced by Sichuan Xincheng Biological Co., LTD: IFP-2000, IFP-3000, Auto- HFIAS 1000, HFD-Station dry fluorescence immunoassay analyzer

Parameter: