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500ul Inflammation Test Kit

Price Negotiable
Price: USD1.0-USD3.5 test
MOQ: 10,000tests
Delivery Time: 3-5 working days
Brand: Diagence
Product Description

Inflammation Kit Serum Amyloid A Test Kit Cassette For Self Use

 

Why we should test SAA

 

SAA is an acute phase protein and binds to plasma high-density lipoprotein (HDL). Now, clinical research focuses on SAA types during the acute reaction of inflammatory diseases. Compared with the well-proven acute phase protein-CRP, SAA is used to test whether it has any advantages in the diagnosis of acute inflammatory diseases. It remains to be determined.
 
Similar to CRP, it is used to assess the progress of acute phase reactions. SAA is a sensitive parameter. It begins to increase after about 8 hours of inflammatory response, and exceeds the upper limit of the reference range earlier than CRP. However, the difference between the median value of CRP in normal people and the upper limit of the reference range is about 10 times. Only 5 times in SAA. For minor infections, for example, many viral infections, elevated SAA is more common than CRP. In infectious diseases, the absolute rise of SAA is higher than that of CRP, so SAA determination, especially for "normal" and minor acute phase reactions, can provide a better distinction. Usually about two-thirds of cold patients have elevated SAA, but less than one-half of patients have the same increase in CRP. In virus infection cases, elevated SAA and CRP concentrations are seen in adenovirus infections.
 
Reference
 
Under normal circumstances, the level of cTnI in peripheral blood is very low: (0 ~ 0.3 μg/L). After the onset of AMI, due to its small molecular weight, it is quickly released from human blood and its concentration rises rapidly. Zaninotto et al. used 1μg/L cTnI as the positive diagnostic threshold. The diagnosis rate of patients with suspected AMI can reach 94.3%, and the diagnosis specificity is 100%.
The reference value of cTnI in peripheral blood under normal conditions: ①0.02~0.13 μg/L.②>0.2 μg/L is the critical value. ③> 0.5 μg/L can diagnose AMI.
 
Name Box Range Time Approved
SAA 31 x 21 x 22 cm 0.5~100 4Min CE/ISO

 

 

 

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