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MALARIA PAN/PF RAPID TEST STRIP | MALARIA RAPID TEST KIT STRIP CASSETTE-25PACK
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KSh2,500.00KSh3,000.00
PRODUCT DESCRIPTION:
- The Malaria P.f. /Pan Rapid Test Cassette(Whole Blood) in Kenya is a qualitative,membrane based immunoassay for the detection of P.f., P.v., P.o. and P.m. antigens in whole blood.
The membrane is pre-coated with anti-HRP-II antibodies and anti-Aldolase antibodies. During testing, the whole blood specimen reacts with the dye conjugate, which has been pre-coated on the test cassette. - The mixture then migrates upward on the membrane by capillary action, reacts with anti-Histidine-Rich Protein II (HRP-II) antibodies on the membrane on P.f. Test Line region and with anti-Aldolase antibodies on the membrane on Pan Line region.If the specimen contains HRP-II or Plasmodium-specific Aldolase or both, a colored line will appear in P.f. line region or Pan line region.
- The absence of the coloredlines in P.f. line region or Pan line region indicates that the specimen does not contain HRP-II
and/or Plasmodium-specific Aldolase.
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MALARIA PAN/PF RAPID TEST KIT STRIPS CASSETTE.
FEATURES:
-The test cassette contains anti-HRP-II of Plasmodium falciparum antibodies conjugated gold and
anti-Plasmodium falciparum Aldolase antibodies conjugated gold and anti-HRP-II antibodies and
anti-Aldolase antibodies coated on the membrane.
PRECAUTIONS:
• For professional in vitro diagnostic use only. Do not use after expiration date.
• For whole blood specimen use only. Do not use other specimens.
• Do not eat, drink or smoke in the area where the specimens or kits are handled.
• Handle all specimens as if they contain infectious agents. Observe established precautions
against microbiological hazards throughout all procedures and follow the standard procedures
for proper disposal of specimens.
• Wear protective clothing such as laboratory coats, disposable gloves and eye protection when
specimens are assayed.
• The used test should be discarded according to local regulations.
• Humidity and temperature can adversely affect results.
• Do not exchange or mix buffer and test cassettes from kits of different lot numbers.
• Caution must be taken at the time of specimen collection. Inadequate volume of specimen may
lead to lower sensitivity.
• Be sure to add sufficient buffer to the cassette’s sample well. Invalid result may occur if
inadequate buffer is added.
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