Product Description
| Brand | SD Biosensor |
| Sample Type | Whole Blood |
| Pack Size | 40T |
| CAT No | RK025-40 |
Standard Q Malaria P.f/P.v is an immunochromatographic assay for the differential detection between Plasmodium falciparum Histidine-Rich Protein II (HRP II) and pLDH (plasmodium lactate dehydrogenase) specific to Plasmodium vivax in human whole blood.This test is intended for professional use,only for an initial screening and reactive specimen should be confirmed by a supplemental assay such as microscopic examination of thin blood smear.
Prompt and Precise Malaria DetectionThe STANDARD Q Malaria P.F/P.V Ag test offers rapid results within 15-20 minutes, allowing healthcare professionals to quickly identify malaria infections caused by P. falciparum and P. vivax. Its high accuracy and inherent quality control make it a reliable choice for frontline disease diagnosis in a wide range of settings.
Easy and Portable Diagnostic SolutionThis malaria rapid diagnostic test is lightweight, compact, and requires no additional equipment or electricity. Its user-friendly design, coupled with single-use cassettes and straightforward visual interpretation, makes it suitable for clinics, laboratories, and field use-even in resource-limited environments.
Stable and Long-Lasting PerformanceWith a shelf life of 24 months and robust storage requirements, the STANDARD Q Malaria test guarantees stable performance when stored between 2-30C. Its durable construction and secure packaging ensure each cassette is ready for accurate use anytime.
FAQ's of SD Biosensor STANDARD Q Malaria P.F/P.V Ag:
Q: How is the SD Biosensor STANDARD Q Malaria P.F/P.V Ag test performed?
A: The test is conducted using a whole blood sample acquired via fingerstick or venous draw. The sample is placed onto the test cassette, followed by a buffer. Results are visually interpreted, with lines indicating positive or negative findings for P. falciparum and P. vivax antigens.
Q: What are the main benefits of using this malaria rapid diagnostic test?
A: Benefits include rapid results within 15-20 minutes, high accuracy, differentiation between P. falciparum and P. vivax, no need for specialized equipment or electricity, and simple operation. It's ideal for field deployment and clinical settings alike.
Q: When should this test be used?
A: This test should be used when malaria infection is suspected in a patient, enabling immediate detection and supporting timely treatment, especially in situations where laboratory microscopy is unavailable or results are needed quickly.
Q: Where can the STANDARD Q Malaria test be utilized?
A: This test is suitable for use in hospitals, clinics, diagnostic laboratories, and field locations-especially where access to electricity and sophisticated lab infrastructure is limited. It is designed for professional use only.
Q: What is the process for interpreting the results?
A: After applying the sample and buffer, wait 15-20 minutes. The appearance of the control line confirms the test is valid. Additional lines in the test area indicate the presence of P. falciparum (HRP2 antigen) and/or P. vivax (pLDH antigen).
Q: How should the test be stored for optimal performance?
A: Keep the test kits at a temperature between 2-30C, away from direct sunlight. Do not freeze the product, and ensure it remains in its original packaging until ready for use.
Q: What ensures the reliability of each test cassette?
A: Every cassette features an integrated control line that serves as an internal quality check. If the control line does not appear, the test is considered invalid and should be repeated with a new cassette.