Ordering Information

Specifications and performance

Operation process

About this test

Malaria is one of humanity's most devastating infectious diseases. The causative agent of malaria is a single-celled protozoan parasite belonging to the genus Plasmodium. These parasites infect not only humans but also other vertebrates, from reptiles and birds to mammals.
The Malaria P.f/P.v Antigen Rapid Test is a rapid lateral flow immunoassay for the qualitative detection of histidine-rich protein II (HRP-II) specific for Plasmodium falciparum (P.f) and Plasmodium vivax (P.v) Lactate dehydrogenase (pLDH) in human whole blood, results can be obtained in 15~30 minutes with minimal technical staff and without any laboratory equipment.

Fast and easy to use

1.This kit is only used for veterinary diagnosis, please operate in strict accordance with the instruction manual.

Positive: Red bands appear in both the test area (T1 line) and the quality control area

(C line). The results show that the sample contains Plasmodium falciparum antigen.

Red bands appear in both the test area (T2 line) and the quality control area (C line) The results show that the sample contains Plasmodium vivax antigen.

Red bands appear in both the test area (T1 and T2 line) and the quality control area (C line) The results show that the sample contains Plasmodium falciparum antigen and

Plasmodium vivax antigen.

Negative: There is no red band appears in the test area (T1 and T2 line), and a red

band appears in the quality control area (C line). The results show that Plasmodium

falciparum antigen or Plasmodium vivax antigen is not detected in the sample.

Invalid: There is no red band in the quality control area (C line), regardless of whether there is a red band in the test area (T line), indicating the test result of the kit is

invalid, and it is recommended to retest.

Operation Suggestions

1. This product is only used for in vitro qualitative diagnosis, please use it within the

validity period.

2. Please read the instructions for use carefully before use and strictly follow the

instructions for use of the kit.

3. Please use it as soon as possible after opening the aluminum foil bag. If you find

that the aluminum foil bag packaging is damaged, please do not use it. Do not use it in an excessively high temperature or humidity and excessively dry environment. The

low-temperature storage kit needs to be restored to room temperature before to avoid moisture absorption.

4. The test of the sample must be carried out in a specific environment, and the blood

sample contacted during the test should be operated in accordance with the inspection

procedures of the infectious disease laboratory.

5. If you are using venous blood, tap the test tube or vial to mix the specimen. Before

aspirating the sample, aspirate the specimen back and forth several times in the

sample addition head.

6. The sample must be stored clean and not reusable to avoid contamination. The test

sample should avoid repeated freezing and thawing, and the sample with bacterial

contamination should not be used for the test. Samples need to be returned to room

temperature before use. Samples and test cards should be treated as infectious

substances and handled according to preventive measures for blood sources of

infection.

7. It should be kept clean, and the pollutants should be treated as waste. Waste

disposal is carried out in accordance with the local national regulations on safe disposal of waste, safe disposal of infectious waste and safe disposal of infectious waste,

please handle with caution.

Operation Flow