Medlera Malaria Pf/Pan Rapid Test

Medlera Malaria Pf/Pan Rapid Test is a rapid immunochromatographic assay for the qualitative detection and differentiation of P.falciparum (HRP-2) and P. falciparum, P. vivax, P. malariae, P. ovale (through pan-pLDH antigens) malaria antigen in human whole blood samples. The test is intended as an aid in the earlier diagnosis of Malaria infection.

Description

01. Comprehensive Malaria Detection:

Medlera Malaria Pf/Pan Rapid Test is an immunochromatographic assay for the qualitative detection and differentiation of P.falciparum (HRP-2) and P. falciparum, P. vivax, P. malariae, P. ovale (through pan-pLDH antigens) malaria antigens in human whole blood samples.

02. Early Diagnosis Aid:

Intended as an aid in the earlier diagnosis of Malaria infection, offering a comprehensive approach to facilitate effective management and monitoring of the condition.

03. Professional Use:

Designed for use by Professional Technical Persons, ensuring accurate and reliable results in a clinical setting.

04. Innovative Single-Well Technology:

Utilizes single-well technology for easier testing, providing convenience and efficiency.

05. Low Sample Volume:

Requires only 5µL of human whole blood samples, reducing discomfort during sample collection.

06. Faster Background Clearance:

Faster and clearer background clearance for quicker and more efficient testing.

07. Monoclonal Antibodies Utilized:

Utilizes monoclonal antibodies to detect and differentiate P.falciparum and P.vivax, P.ovale & P.malariae parasites, ensuring accuracy.

08. Lowest Detection Limit:

Has the lowest detection limit among all industry standards, capable of detecting 35 p/µL of the sample.

09. Rapid Results:

Confirm results in 25 minutes, providing quick and reliable diagnostic information.

 

Additional information

What is detected

P.falciparum (HRP-2) and P. falciparum, P. vivax, P. malariae, P. ovale (through pan-pLDH antigens) malaria antigen

Its function

Aid in management and monitoring of Malaria infection

The type of specimen required

human whole blood samples

The intended user

Professional Technical Person

Sensitivity of Test

100%

Specificity of Test

100%