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Cassette Dengue NS1 Rapid Test Kit Whole Blood Serum Plasma Antigen Diagnostic Kit

Labnovation Technologies, Inc.
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Address: 101 and 5th Floor, Building 1, No. 68,18th Road, Guangming Hi-Tech Park, Tangjia Community, Fenghuang Street, Guangming District, Shenzhen 518107 ,China

Contact name:Aimee li

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Labnovation Technologies, Inc.

Cassette Dengue NS1 Rapid Test Kit Whole Blood Serum Plasma Antigen Diagnostic Kit

Country/Region china
City & Province shenzhen
Categories Dyestuff Intermediates
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Product Details

Rapid Antigen Test Kit Dengue NS1 Antigen Rapid Test Kit High Accuracy Antigen Rapid Test Kit

 

Intenden Use

The Dengue NS1 Antigen Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection dengue virus NS1 antigen to dengue virus in serum/plasma/whole blood to aid in the diagnosis of Dengue viral infection.

Specifications

Test ItemDengue NS1 Antigen Rapid Test Kit
Number LQ-000102
Sample TypeSerum, Plasma, Whole Blood
Product Shelf Life24 Months
Test SpeedWithin 15 minutes
Sample Volume3 Drops(80μl-100μl)
Package25 Tests/Box
Storage ConditionStore 2-30℃
Humidity≤60%
Sensitivity97.92%
Specificity99.02%
Accuracy98.67%

Main Components

  • 25 Test Cassette
  • 25 Disposable Pipette
  • 1 Specimen Buffer
  • 1 Package Insert

Material Needed But Not Provided

  • Specimen Collection Containers
  • Centrifuge (for serum/plasma sample)
  • Timer

Analytical Resualts

  • Specificity: 99.02%
  • Sensitivity: 97.92%
  • Accuracy: 98.67%

Use Step

  • Take off the outer packing, put the cassette onto the desk with the sample window up.
  • Drop 3 drops (80μl-100μl) of serum/plasma/whole blood vertically into the sample well of cassette. If the whole blood sample is thick, add 1 drop (40-50μl) of specimen buffer into the sample well of cassette.
  • Observe the test results immediately within 15-20 minutes, the result is invalid after 20 minutes.

Interpreation Of Result

  • POSITIVE: Two distinct red lines appear. One line should be in the control region (C) and the other line should be in the test region (T).

  • NEGATIVE: One red line appears in the control region(C). No apparent red or pink line appears in the test region (T).

  • INVALID: No red lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.

Precautions

  1. For IN VITRO diagnose only.
  2. Do not use after the expiration date.
  3. The test result is invalid over 20 minutes.
  4. All samples and reagents should be considered potentially hazardous and handled in the same manner as an infectious agent after use.
  5. The strength of the quality control line does not indicate the quality problem of the reagent, a test result that is clearly visible demonstrates the reagent is effective.
  6. Do not use other kinds of quality control sample to test the reagent. Components of different batches cannot be exchanged for use to avoid erroneous results.

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