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Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats

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Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats

Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats
Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats

Large Image :  Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats

Product Details:
Place of Origin: China
Brand Name: DVOT
Certification: CE/BfArM/ PEI
Model Number: Malaria Pf/Pan Rapid Test
Document: Product Brochure PDF
Payment & Shipping Terms:
Minimum Order Quantity: 1250Test
Price: 0.17~0.23USD per Test
Packaging Details: Each boxes 25tests
Delivery Time: 5-8 Working days
Payment Terms: T/T, Western Union
Supply Ability: 1000000pcs

Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats

Description
Product Name: Malaria Pf/Pan Rapid Test Formats: Cassette
Reaction Time: 10-15 Minutes Shelf Life: 24 Months At Room Temperature 4- 30 Degrees
Others: The Kits Can Be Made According To The Customers' Artwork Or Design Time Of Use: Disposable
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Whole Blood Malaria Pf/Pan Rapid Test

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Malaria Pf/Pan Rapid Test Cassette

Rapid And Efficient Detection Reagent For Malaria Pf/Pan

 

 

     The Malaria Pf/Pan Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of circulating antigens of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae in whole blood.

 

Detection Principle

 

      The Malaria Pf/Pan Rapid Test Device (Whole Blood) 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‐Lactate Dehydrogenase antibodies. During testing, the whole blood specimen reacts with the dye conjugate, which has been pre‐coated on the test strip. 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‐Lactate Dehydrogenase antibodies on the membrane on Pan Line region. If the specimen contains HRP‐II or Plasmodium‐ specific Lactate Dehydrogenase or both, a colored line will appear in P.f line region or Pan line region or two colored lines will appear in P.f line region and Pan line region. The absence of the colored lines in P.f line region or Pan line region indicates that the specimen does not contain HRP‐II and/or Plasmodium‐specific Lactate Dehydrogenase. To serve as a procedure control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

 

STORAGE AND STABILITY

 

The kit can be stored at room temperature or refrigerated (2‐30°C). The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.

 

PROCEDURE

 

Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature (15‐30°C) prior to testing.

  1.  Remove the test device from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour.
  2.  Place the test device on a clean and level surface. Transfer the specimen by a pipette or a dropper:
  • To use a Pipette: Transfer 5ul of whole blood to specimen well of the test device, and then add 3 drops of buffer (approximately 180ul) to the buffer well, and start the timer.
  • To use a Disposable Specimen Dropper: Hold the dropper vertically; draw the specimen up to the Fill Line (approximately 5ul). Transfer the specimen to the specimen well, then add 3 drops of buffer (approximately 180ul) to the buffer well and start the timer.

      3. Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.

 

 

INTERPRETATION OF RESULTS

 

Whole Blood Malaria Pf/Pan Rapid Test Device Cassette Formats 0

 

LIMITATIONS OF THE TEST

  1. The Malaria Pf/ Pan Rapid Test Device (Whole Blood) is for in vitro diagnostic use only. This test should be used for the detection of P.f, P.v, P.o, P.m antigens in whole blood specimens only. Neither the quantitative value nor the rate of increase in P.f, P.v, P.o, and P.m concentration can be determined by this qualitative test. 
  2. The Malaria Pf/ Pan Rapid Test Device (Whole Blood) will only indicate the presence of antigens of Plasmodium sp. (P.f, P.v, P.o, P.m) in the specimen and should not be used as the sole criterion for the diagnosis of malaria infection. 
  3. As with all diagnostic tests, all results must be interpreted together with other clinical information available to the physician. 
  4. If the test result is negative and clinical symptoms persist, additional testing using other clinical methods is recommended. A negative result does not at any time preclude the possibility of malaria infection.

 

KIT COMPONENTS

  • Test Devices 
  • Disposable specimen droppers 
  • Buffer 
  • Package insert

MATERIALS REQUIRED BUT NOT PROVIDED

  • Pipette and disposable tips (optional) 
  • Specimen collection containers 
  • Lancets (for fingerstick whole blood only) 
  • Timer

 

 

 

 

 

 

 

 

 

 

Contact Details
Shenzhen Emeng Health Technology Co., LTD

Contact Person: Mr. Kayla YI

Tel: +86 13760822077

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