Tuberculosis Blood Test - Efficient and Quick 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

Experience the revolutionary Filariasis IgG/IgM Rapid Test Device from QL Biotech - tailored specifically to aid in the accurate diagnosis of Tuberculosis. This superior piece of technology has been ingeniously designed with a keen focus on ease of use and promptness of results. The Tuberculosis Blood Test can be conducted using different specimens, including Whole Blood, Serum, or Plasma, offering versatility and accommodating various medical or clinical settings. Our rapid test device guarantees results within a 15-minute timeframe - a feature that sets it apart in today's healthcare industry. This remarkable quick response time could be a game-changer in the management and control of Tuberculosis, especially in time-sensitive situations. QL Biotech, as a reputable brand in the biotechnology industry, ensures the highest quality in all our products. This Filariasis IgG/IgM Rapid Test Device is no different. We're confident in its ability to deliver accurate and rapid diagnostic results for Tuberculosis, contributing to the timely and effective treatment of the disease.

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.



In the fast-paced world of healthcare, our Tuberculosis Blood Test device serves as a reliable tool for healthcare professionals, elevating the standard of care and contributing to better patient outcomes. With its straightforward operation and speed of diagnosis, it significantly reduces the waiting time for results, offering a seamless user experience. Elevate your diagnostic accuracy and speed with QL Biotech's Filariasis IgG/IgM Rapid Test Device, the perfect ally in the fight against Tuberculosis. Embrace the future of healthcare diagnostics today with QL Biotech. Discover the difference with our Tuberculosis Blood Test - because every second counts in making a diagnosis.

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