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One step test for CK-MB/ctnI/Myo (Colloidal Gold)

One step test for CK-MB/ctnI/Myo (Colloidal Gold)

Product code: 2765
Commitment to quality
Commitment to quality
The product is exactly as described on the website.
Warranty up to 10 years
Warranty up to 10 years
Lifetime product warranty
Easy Payment
Easy Payment
Accept Visa + Credit card

Product information

Manufacturer: Getein Biotechnology Co., Ltd (Nanjing, China)
 
 
The CK-MB/cTnI/Myo Rapid Test Kit (colloidal gold essence) applies immunochromatography to detect concentrations in serum, plasma or in whole blood samples. The rapid test kit gives quick results within 10-20 minutes with higher accuracy for diagnosis and treatment.

 

The quality of products:

 

For fast results within 8-18 minutes with higher accuracy for diagnosis and treatment.

 

Uses:

 

CK-MB/cTnI/Myo Rapid Test Kit (colloidal gold essence) applies immunochromatography to detect the concentration of CK-MB/cTnI/Myo in serum, plasma or in whole blood samples.

 

This test is performed to assist in the analysis and clinical diagnosis of diseases associated with myocardial injury such as acute myocardial infarction, angina, acute myocarditis, and syndromes and syndromes. acute coronary artery.

 

Application:

 

Widely used in emergency rooms, laboratories, cardiology, cardiac surgeries, public health institutes, on-site treatment emergencies, providing rapid diagnosis for patients.

 

Test rule:

 

The CK-MB/cTnI/Myo test uses 1 monoclonal CK-MB/cTnI/Myo antibody conjugated with colloidal gold and another monoclonal antibody coated on the test result line.

 

After the sample is injected into the test tube, the monoclonal antibody CK-MB/cTnI/Myo labeled with colloidal gold will combine with CK-MB/cTnI/Myo in the sample to form an antigen-antibody complex. .

 

This complex will migrate to the test tag analysis area by capillary action and will encounter the immobilized antibody on the membrane to produce a red line on the test result line.

 

The intensity of the color on the result line is proportional to the concentration of CK-MB/ cTnI/ Myo.

 

Then insert this test result barcode into the FIA8000 quantitative immunoassay device, the concentration of CK-MB/ cTnI/ Myo will be measured and displayed on the screen.

 

CK-MB/cTnI/Myo concentrations are stored in the FIA8000 and are readily displayed when required.

 

Results will be able to be transferred to laboratory or hospital information systems if these systems are connected to the FIA8000.

 

Warnings and cautions:

 

Diagnosis in vitro.

 

Used by medical professionals.

 

Do not use the kit after the expiry date printed on the outside of the box packaging.

 

Store test cards in sealed bags until needed. The test card can only be used once.

 

The straw should only be used for 1 sampling. Do not reuse.

 

Specimens, test cards and straws are highly infectious. Therefore, it is necessary to have appropriate treatment and disposal methods according to local regulations to avoid this situation.

 

Use caution and strictly follow the instructions for use.