Hangzhou Funworld Biotech Co.,Ltd

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

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Hangzhou Funworld Biotech Co.,Ltd
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Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

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Malaria Pf/Pv Rapid Test Device(Whole Blood)

FOB Price : Get a Price/Quote

Min.Order : 1000 Piece(s)

Certification : ISO13485,CE

Brand Name : Funworld

Payment Terms : T/T,D/P

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product information

  • brand name : Funworld

  • certification : ISO13485,CE

  • min.order : 1000 Piece(s)

  • warranty : 2 years

  • payment terms : T/T,D/P

  • Packaging : Standard Export Carton

  • Specification : 25 Tests/ box

  • place of origin : China

product description

The Malaria P.f./P.v. Rapid Test Device (Whole Blood) is a qualitative, membrane based immunoassay for the detection of P.f and P.v antigens in whole blood. The membrane is pre‐coated with anti‐HRP‐II antibodies and anti‐pLDH 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‐pLDH antibodies on the membrane on P.v. Line region. If the specimen contains HRP‐II or Plasmodium‐specific P.vivaLDH or both, a colored line will appear in P.f line region or P.v. line region or two colored lines will appear in P.f line region and P.v. line region. The absence of the colored lines in P.f line region or P.v. line region indicates that the specimen does not contain HRP‐II and/or Plasmodium‐specific P.vivaLDH. 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. 

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Malaria Pf/Pv Rapid Test Device(Whole Blood)
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product information

product description

The Malaria P.f./P.v. Rapid Test Device (Whole Blood) is a qualitative, membrane based immunoassay for the detection of P.f and P.v antigens in whole blood. The membrane is pre‐coated with anti‐HRP‐II antibodies and anti‐pLDH 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‐pLDH antibodies on the membrane on P.v. Line region. If the specimen contains HRP‐II or Plasmodium‐specific P.vivaLDH or both, a colored line will appear in P.f line region or P.v. line region or two colored lines will appear in P.f line region and P.v. line region. The absence of the colored lines in P.f line region or P.v. line region indicates that the specimen does not contain HRP‐II and/or Plasmodium‐specific P.vivaLDH. 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. 

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