Professional Manufacturer of Rapid Test Devices
|Place of Origin:||China|
|Certification:||ISO9001, CE, TUV, FDA|
|Model Number:||HEV (Hepatitis E Virus)|
|Minimum Order Quantity:||10 Boxes or 400 Kits (40 Kits/Box)|
|Price:||Negotiable as per Order Quantity|
|Packaging Details:||40 Kits/Box, 50 Boxes/Carton, 317g/Box, 18kgs/Carton, Box Size: 250x125x65mm, Carton Size: 650x510x330mm|
|Delivery Time:||8 days|
|Payment Terms:||T/T, Western Union, MoneyGram|
|Supply Ability:||100,000 Kits Per Day|
|Result Time:||5-30 Minutes||Accuracy:||99%|
|Shelf Life:||2 Years||Certifite:||ISO9001, CE, TUV, FDA|
30 Minutes HEV Rapid Test Cassette,
FDA HEV Rapid Test Cassette,
Plasma HEV Rapid Test Cassette
HEV(Hepatitis E Virus) Antibody Rapid Diagnostic Kit (Colloidal Gold)
For the qualitative detection of HEV antibodies in serum and plasma
☀ High Sensitivity: 100%
☀ Specificity: 100%
☀ Reliable: Accuracy higher than 99%, early detection of the presence of HEV Antibody
☀ Convenient: Room Temperature Storage, Built-In Control Line
☀ Certified by Authoritative Certification System and Standards
☀ Fast: Results in 5-30 minutes, strong positive results may be observed promptly within 3 minutes
☀ Simple: No Instrument Required
☀ Winner of "the National Rapid Diagnostic Kit for Clinical Performance Assessment"
Diagnostic Kit for Hepatitis E Virus Antibody (Colloidal Gold) is a Chromatographic immunoassay (CIA) for direct qualitative detection of antibodies to Hepatitis E type virus (HEV) in human serum and plasma .
Diagnostic Kit for Hepatitis E Virus Antibody (Colloidal Gold) is a chromatographic immunoassay (CIA) for the detection of antibodies to HEV in human serum and plasma. HEV recombinant antigens are precoated onto membrane as a capture reagent on the test region.
During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HEV recombinant antigens. If antibodies to HEV are present, a pink colored band will develop on the membrane in proportion to the amount of HEV antibodies present in the specimen.
Absence of this pink colored band in the test region suggests a negative result.
To serve as a procedural control, a pink colored band in the control region will always appear regardless the presence of antibodies to HEV.
Reagents and Materials Provided
☀ Blood diluent in a dropper bottle. Store at 4-30°C.
☀ One sealed pouched cassette with desiccant & disposable pipe
☀ One piece of operating instruction with 40 test pouches.
Sample Collection and Preparation
☀ Have a certified phlebotomist collect whole blood into a red top collection tube (containing no anticoagulants) by veinpuncture.
☀ Allow the blood to clot.
☀ Separate the serum by centrifugation.
☀ Carefully withdraw the serum for testing or label and store it at 2-8°C for up to 7 days. Serum may be frozen at -20°C for at least three month.
☀ Have a certified phlebotomist collect whole blood into a purple, blue or green top collection tube (containing EDTA, citrate or heparin, respectively) by veinpuncture.
☀ Separate the plasma by centrifugation.
☀ Carefully withdraw the plasma for testing, or label and store it at 2-8°C for up to 7 days. Plasma may be frozen at -20°C for at least three months
Serum or Plasma Sample
Add 5ul of serum or plasma into sample well, and 80-100 ul buffer into B well. Observe the result in 20 minutes.
Interpretation of Results
|No apparent band in the test region (T), a pink-colored band appears in the control region (C). This indicates that no HEV antibody has been detected.|
|In addition to a pink-colored band in the control region (C), a pink-colored band will appear in the test region (T). This indicates that the specimen contains HEV antibodies.|
|If no band appears in the control region (C), regardless of the presence or absence of line in the test region (T). It indicates a possible error in performing the test. The test should be repeated using a new device.|
Store the test kits at temperature 4-30°C, in the sealed pouch for the duration of the shelf life (24 months).
Warning and Precautions
☀ For in vitro diagnostic uses only.
☀ Do not interchange reagents from different lots. Do not use test kit beyond expiration date.
☀ All patient samples should be treated as if capable of transmitting diseases.
☀ Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
Contact Person: Mr. Randy.Zhang