β2-MG test Rapid Test poct Kits

β2-MG test Rapid Test poct Kits

Methodology                                                                                

Fluorescence Immunoassay

β2-MG is important indicator to reflect glomerular filtration rate, renal transplantation, renal function, with higher analytical sensitivity, wider of lower detection line, lower concentration values for better precision, and more efficient operation.

Product Name                                                                              

General Name:β2-MG Test Kit(Immunofluorescence)

Package                                                                                           

Test card: Aluminum foil pouch 1pc/bag, desiccant

Package size: 25pcs/box

Interpretation of test results                                                 

1.The analysis of test results are accomplished by  immune-fluorescence  quantitative

   analyzer of  our company's NORMAN series.

2.The concentration of β2-MG in the unknown samples can be read directly in the    

    corresponding batch of ID card standard curve by fluorescence signal value we

    measured. The default results use mg/L as a unit.

Performance Indicators                                                          

1.Detection limit: ≤0.1 mg/L.

2.Linear range:0.1-20mg/L, the linear correlation coefficient r should not be less than  

   0.9900 in this range.

3.Accuracy: Recovery rate is within the range (80% ~ 120%).

4.Repeatability: CV≤15%.

5.Difference between batches: CV≤15%.

Expected values/Reference range                                       

The reference range study was conducted based on β2-MG content of 95% of the 

distribution range of statistical analysis in 120 healthy people, the result was as follows:

It is recommended that each laboratory established its own reference range, which may 

be unique to the population it serves depending upon geographical, patient, dietary, or 

environmental factors.

Notice Of  Detection Result                                                    

1.The test results should take clinical symptoms,health history,other laboratory tests, 

   etc. into account, just for clinical reference, nor as a sole factor of clinical diagnostic.

2.All operation must be strictly in accordance with operating procedures to get the correct

   result. The accuracy of test results may be affected by any changes to operational 

   procedures.

Clinical Significance                                                                  

Sample       reference range (mg/L)

Serum         1.01-2.97

Urine          0.10-0.30

Product Advantage                                                                    

Strong anti-interference ability

Different sample types: serum, urine

Wide test range:0.1-20mg/L

High sensitivity,

Good repeatability

Single sample test or batch test.

Package & Delivery                                                                    

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About Us                                                                                        

Nanjing Norman Biological Technology Co., Ltd is dedicated to R&D and manufacturing of automated chemiluminescence system. Founded in 2008, Norman biological has been upholding the idea that R&D shapes future ,and concentration determines success. Ever since the beginning, Norman has been focusing on developing and manufacturing chemiluminescence instruments and reagents.

Norman's manufacture center is located in the Yuhua District and owns an over 2,000m2 GMP-approved clean workshop. The R&D base, which is over 2,000m2 , is located in state-level new Jiangbei district. Now there are over 100 R&D engineers, 40% of which hold a PhD or master's degree.

R&D shapes future, and concentration determines success. Driven by the commitment to "provide complete solution to improve human health", Norman will consistently do its utmost to drive the IVD industry forward and contribute more to human health.

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If you are interested in working with us, please feel free to contact.