Minimum Order Quantity
1 Kit

मुख्य निर्यात बाजार
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मुख्य घरेलू बाज़ार

Malaria P.f/P.v Ag qualitatively analyzes Plasmodium falciparum and Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.

Accurate Dual Detection

This rapid test kit identifies both Plasmodium falciparum and Plasmodium vivax antigens, supporting prompt and appropriate malaria treatment. High sensitivity and specificity ensure reliable diagnostics for healthcare providers, improving the accuracy of patient care.

Ease of Use and Fast Results

With a simple procedure requiring only 5 L of whole blood, professionals can conduct tests efficiently. Results are available in just 15 minutes, aiding timely clinical decision-making, particularly in laboratory or high-throughput settings.

Comprehensive Kit and Clear Controls

Each kit contains all essential components, including cassettes with visible expiry dates and built-in controls for procedural verification. This ensures every test performed maintains consistent quality, enhancing safety and reliability.

FAQs of MALARIA Pf/ Pv Ag RAPID TEST:

Q: How is the MALARIA Pf/Pv Ag RAPID TEST performed?

A: The test requires collecting 5 L of whole blood and adding it, along with assay buffer, to the cassette. Results can be read visibly after 15 minutes, with internal control lines confirming test validity.

Q: What samples are needed for this malaria rapid test?

A: This assay is designed to use whole blood, obtained from patients suspected of having malaria. Only 5 L of blood is required for each test, minimizing patient discomfort and sample preparation time.

Q: When can results from the MALARIA Pf/Pv Ag RAPID TEST be seen?

A: Test results are available within 15 minutes after the addition of the sample and buffer to the cassette, enabling rapid diagnosis and treatment decisions.

Q: Where is this test suitable for use?

A: The kit is intended for professional and laboratory use, including hospitals, clinics, and diagnostic centers, and is supplied by exporters and manufacturers based in India.

Q: What is the benefit of using a built-in procedural control line?

A: The control line ensures that each test is performed correctly, indicating whether the assay has functioned as intended. This feature increases confidence in the accuracy and reliability of results.

Q: How do I ensure the test has not expired before use?

A: Each test cassette displays a visible expiry date. Always check this date prior to performing any test to guarantee the effectiveness and validity of the assay.

Q: What is included in the MALARIA Pf/Pv Ag RAPID TEST kit?

A: Each kit contains 25 test cassettes, droppers, assay buffer, and a package insert detailing instructions for use, offering a comprehensive solution for malaria antigen detection.