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5 in 1 Diagnostic Toxo/Rubella/Cmv/Hsv1/2 Igg/Igm Test Kit

Short Description:

  • Format: cassette
  • Specifications: 25t/box
  • Specimen: Whole Blood,serum, plasma
  • Reading Time: 15 minutes
  • Storage Condition: 4-30ºC
  • Shelf Life: 2 years
  • Ingredients and Content
  1. Rapid Test Cassette(25 bags/ box)
  2. Dropper (1 pc/bag)
  3. Desiccant (1 pc/bag)
  4. Diluent (25 bottles/box, 1.0mL/ bottle)
  5. Instruction (1 pc/box)

 


  • FOB Price: US $0.5 - 9,999 / Piece
  • Min.Order Quantity: 5000 Pcs/Order
  • Supply Ability: 100000 Piece/Pieces per Month
  • Product Detail

    Product Tags

    Product name

    5 in 1 Diagnostic Toxo/Rubella/Cmv/Hsv1/2 Igg/Igm Test Kit

     Sample type : Whole Blood,serum, plasma

     [Intended use]

    Toxoplasma gondii (Toxo), Rubella virus (Rubella), Cytomegalovirus (CMV) and Herpes simplex virus 1/2 (HSV 1/2)

    It is suitable for the rapid detection of   Toxo/Rubella/Cmv/Hsv1/2 in human  whole blood ,serum, plasma samples.

    [Usage]

    Read the IFU completely before testing, allow the test device and specimens to equilibrate to room temperature (15~25) prior to testing.

    Method : 

    [Result judgment]

    • Positive: Control line and at least one test line appear on the membrane.The appearance of lgG test line indicates the presence of ToRCH specificlgG antibodies. The appearance of lgM test line indicates the presence ofToRCH specific lgM antibodies. And if both lgM and IgG line appear, itindicates that the presence of both ToRCH specific lgG and lgM antibodies.
    • Negative: One colored line appears in the control region(C).No apparentcolored line appears in the test line region.
    • Invalid: Control line fails to appear. Insufficient specimen volume orincorrect procedural techniques are the most likely reasons for control linefailure. Review the procedure and repeat the test using a new test cassette.lf the problem persists, discontinue using the lot immediately and contactyour local distributor.

    [Precautions]
    1. Please use the test card within the guarantee period and within one hour after opening:
    2. When testing to avoid direct sunlight and electric fan blowing;
    3. Try not to touch the white film surface in the center of the detection card;
    4. Sample dropper cannot be mixed, so as to avoid cross contamination;
    5. Do not use sample diluent that is not supplied with this reagent;
    6. After the use of detection card should be regarded as microbial dangerous goods processing;
    [Application limitations]
    This product is an immunological diagnostic kit and is only used to provide qualitative test results for clinical detection of pet diseases. If there is any doubt about the test results, please use other diagnostic methods (such as PCR, pathogen isolation test, etc.) to make further analysis and diagnosis of the detected samples. Consult your local veterinarian for pathological analysis.

     


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