Rapid Gonorrhea Test Cassette by QL Biotech: Filariasis IgG/IgM Detection

Short Description:

The Filariasis IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-lymphatic filarial parasites (W. Bancrofti and B. Malayi) in human serum, plasma or whole blood. This test is intended to be used as a screening test and as an aid in the diagnosis of infection with lymphatic filarial parasites. Any reactive specimen with the Filariasis IgG/IgM Rapid Test must be confirmed with alternative testing method(s).


Product Detail

Product Tags

Discover the ease and efficiency of diagnosing Filariasis with QL Biotech's Gonorrhea Test Cassette - a unique device designed to rapidly detect Filariasis IgG/IgM from whole blood, serum, or plasma samples. The Gonorrhea Test Cassette is an innovative product from QL, a renowned brand in the biotech industry known for its reliable and high-quality medical devices. The Gonorrhea Test Cassette leverages advanced biotech to deliver results in just 15 minutes, revolutionizing the field of disease detection. It is incredibly straightforward to use, making it ideal for medical professionals. The device offers enhanced accuracy and speed, traits that are essential in today's fast-paced medical world. With QL Biotech's Gonorrhea Test Cassette, you can rest assured that disease detection is accurate and rapid. It eliminates the need for lengthy laboratory tests and is a convenient product for swift on-site diagnostic testing. This Filariasis IgG/IgM Rapid Test Device is a testament to QL's commitment to developing pioneering biotechnological products that empower healthcare professionals and improve patient care.

Product Detail

Brand: QL

Specimens: : Whole Blood/Serum/Plasma

Reading time: in 15 minutes.

Pack:25 T

STORAGE  2‐30°C

KIT COMPONENTS(Device)

Individually packed test devices

Each device contains a strip with colored conjugates

and reactive reagents pre-spreaded at the

corresponding regions

Disposable pipettes

For adding specimens use

Buffer

Phosphate buffered saline and preservative

Package insert

For operation instruction

SUMMARY AND EXPLANATION OF THE TEST

The lymphatic filariasis known as Elephantiasis, mainly caused by W. bancrofti and B. malayi, affects about 120 million people over 80 countries1,2. The disease is transmitted to humans by

the bites of infected mosquitoes within which the microflariae sucked from an infected human subject develops into third-stage larvae. Generally, repeated and prolonged exposure to infected larvae is required for establishment of human infection.

The definitive parasitologic diagnosis is the demonstration of microflariae in blood samples3.

However, this gold standard test is restricted by the requirement for nocturnal blood collection and lack of adequate sensitivity. Detection of circulating antigens is commercially available. Its

usefulness is limited for W. bancrofti4. In addition, microfilaremia and antigenemia develop from months to years after exposure.

Antibody detection provides an early means to detect filarial parasite infection. Presence of IgM to the parasite antigens suggest current infection, whereas, IgG corresponds to late stage of infection or past infection5. Furthermore, identification of conserved antigens allows ‘pan-filaria’ test to be applicable. Utilization of recombinant proteins eliminates cross-reaction with

individuals having other parasitic diseases6. The Filariasis IgG/IgM Rapid Test uses conserved recombinant antigens to simultaneously detect IgG and IgM to the W. bancrofti and B. malayi parasites without the restriction on specimen collection.

ASSAY PROCEDURE

Bring the specimen and test components to room temperature if refrigerated or frozen. Place the test device on a clean, flat surface.
For whole blood test

Apply 1 drop of whole blood (about 40-50 µL) into the sample well. Then add 1 drop (about 35-50 µL) of Sample Diluent immediately.

For serum or plasma test

Fill the pipette dropper with the specimen. Holding the dropper vertically, dispense 1 drop (about 30-45 µL) of specimen into the sample well making sure that there are no air bubbles.

Then add 1 drop (about 35-50 µL) of Sample Diluent immediately.

Set up timer. Results can be read in 15 minutes. Positive results can be visible in as short as 1 minute. Don’t read result after 15 minutes.

INTERPRETATION OF ASSAY RESULT


1.In addition to the presence of C band, if only T1 band is  developed, the test indicates for the presence of anti-W. bancrofti  or B. malayi IgG antibody. The result is positive.
2.In addition to the presence of C band, if only T2 band is  developed, the test indicates for the presence of anti-W. bancrofti  or B. malayi IgM antibody. The result is positive.
3.In addition to the presence of C band, both T1 and T2 bands are  developed, the test indicates for the presence of both IgG and IgM  anti-W. bancrofti or B. malayi. The result is also positive.



If only the C band is present, the absence of any burgundy color in the both test bands (T1 and T2) indicates that no anti-W. bancrofti or -B. malayi antibody is detected in the specimen. The

result is negative.

If no C band is developed, the assay is invalid regardless of any burgundy color in the test bands. Repeat the assay with a new device.



QL Biotech is a leading player in the biotech industry, known for integrating innovative technologies into its products. The Gonorrhea Test Cassette is a prime example of this commitment to innovation. It is a powerful tool in the hands of medical professionals, enabling them to diagnose Filariasis effectively and efficiently. In conclusion, the Gonorrhea Test Cassette from QL Biotech simplifies the diagnostic process, making it swift and accurate. It's time to step up your medical practice with this Filariasis IgG/IgM Rapid Test Device and experience quality, efficiency, and reliability like never before. Embrace the future of biotech with QL.

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