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AllTest Mycoplasma Pneumonia IgM Antibody Lateral Flow Immunochromatographic Assays Rapid Test

Basic Information
Place of Origin: CHINA
Brand Name: AllTest
Certification: CE
Model Number: cassette(IMPM-402)
Minimum Order Quantity: 500
Packaging Details: 40T/Kit
Supply Ability: 100 Million a year
Format: Cassette Specimen: Whole Blood,serum,plasma
Kit Size: 40T/Kit Cut-Off: See Insert
Storage: 2-30℃ Shelf Time: 24 Months
High Light:

rapid test kit

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infectious disease diagnostic tests

 

AllTest Mycoplasma Pneumonia IgM Lateral Flow Immunochromatographic Assays Rapid Test

 

 

Applications:

 

The Mycoplasma Pneumonia Antibody Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Mycoplasma Pneumonia in whole blood, serum, or plasma to aid in the diagnosis of Mycoplasma Pneumonia infection.

 

 

Description:

 

Mycoplasma Pneumonia is the causative agent of respiratory tract nfectious diseases and complication of other systems. There will be a symptom with headache, fever, dry cough, and muscle pain. People of all age groups can be infected while youth, middle-aged and children under 4 years old have a higher infection rate. 30% of the infected population may have a whole lung infection.

In normal infection, MP-IgG can be detected as early as 3 weeks after infected, continue to rise very rapidly for a long term, peaking in about 5 weeks. Simultaneous detection of MP-IgG infection can improve the detection rate of MP infection.

 

 

How to use?

 

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.

 

 

INTERPRETATION OF RESULTS

(Please refer to the illustration above)

 

POSITIVE:* Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the test region (T).

 

*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of Mycoplasma Penumonia antibody present in the specimen. Therefore, any shade of color in the test region (T) should be considered positive.

 

NEGATIVE: One colored line appears in the control region (C). No apparent colored line appears in the test region (T).

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test cassette. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

 

Contact Details
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Phone Number : +8615857153722

WhatsApp : +8613989889852