Product Description
ULTRA Malaria P.F/P.V Ag
Ultra Malaria P.f/Pv 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.
| Title | Detail |
| Format | Immunochromatographic Assay |
| Sample Type | Whole blood |
| Sample Volume | 3µl |
| Detects | Histidine-Rich Protein-II from (Plasmodium falciparum)& lactate dehydrogenase from (Plasmodium vivax) |
| Immobilized Material | Monoclonal anti- P.falciparum HRP- 2 & Monoclonal anti- P.vivax pLDH |
| Storage Temperature | 2-40C/36-104F |
| Shelf Life | 24 months |
| Performance | Sensitivity:-100%, Specificity:-100% |
Technical Details 
Reliable Detection in MinutesThe ULTRA Malaria P.f/P.v Ag test offers rapid, accurate detection for both P. falciparum and P. vivax malaria strains in as little as 15 minutes. Its immunochromatographic technology provides clear visual endpoint results, ensuring quick clinical decisions at the point of care. The kit includes all components needed for testing, making it highly suitable for diverse clinical and field environments.
Easy, Professional UseDesigned for professional in vitro diagnostic applications, the device uses whole blood samples from either fingerstick or venipuncture. Its user-friendly operation involves applying blood, adding buffer, and reading results-all without the need for special instrumentation. Each test is individually packaged with complete accessories and instructions, enhancing convenience and reducing cross-contamination risks.
Ideal for Challenging EnvironmentsWith a portable, lightweight design and storage requirements of 2-30C, the test is suitable for various settings, including remote or resource-limited areas. The long shelf life and disposable format allow medical professionals, suppliers, and distributors to confidently stock and use the test with minimal logistical constraints.
FAQ's of SD BIOSENSOR ULTRA Malaria P.f/P.v Ag:
Q: How is the SD BIOSENSOR ULTRA Malaria P.f/P.v Ag test performed?
A: The test is carried out by collecting a whole blood sample from a fingerstick or venipuncture, applying it to the device's test strip, adding the supplied buffer, and interpreting the visual result within 15 minutes, following the included instructions.
Q: What does the ULTRA Malaria P.f/P.v Ag test detect?
A: This test specifically detects antigens from Plasmodium falciparum and Plasmodium vivax, enabling the qualitative identification of these malaria species within a patient's blood sample.
Q: When should this malaria test be used?
A: The test should be used when rapid identification of malaria infections is clinically indicated, such as in symptomatic individuals, during malaria outbreaks, or routine screening in endemic regions by healthcare professionals.
Q: Where can the test be used most effectively?
A: The test is designed for professional settings, including clinics, hospitals, field hospitals, or remote healthcare centers, especially where quick diagnostic turnaround is critical and laboratory infrastructure may be limited.
Q: What are the benefits of using this rapid malaria test?
A: Benefits include rapid results within 15 minutes, high sensitivity and specificity for both P. falciparum and P. vivax, ease of use without special equipment, and suitability for a wide range of environments due to its portability and extended shelf life.
Q: How should the test kits be stored and handled?
A: Store the kits at temperatures between 2C and 30C, avoiding freezing. Each kit is individually packaged with desiccant and should be kept sealed until use to maintain product integrity.