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95% Accuracy White Dengue NS1 Antigen Test Kit Rapid Chromatographic Immunoassay

Categories Dengue NS1 Rapid Test Kit
Brand Name: LABNOVATION
Model Number: LQ-000102
Certification: ISO13485, ISO9001,
Place of Origin: China
MOQ: 10000/Pcs
Price: US$0.4-0.8/pcs
Payment Terms: D/A, D/P, T/T
Supply Ability: 500000/Day
Delivery Time: 5-7 work day
Packaging Details: Carton
Accuracy: >95%
Shele Life: 24 Months
Specimen: Serum, Plasma, Whole Blood
Group: All
Color: White
OEM ODM: Yes
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95% Accuracy White Dengue NS1 Antigen Test Kit Rapid Chromatographic Immunoassay

Dengue NS1 Antigen Rapid Test Kit

(Immunochromatography)


Specifications

Test ItemDengue NS1 Antigen Rapid Test Kit
Sample TypeSerum, Plasma, Whole Blood
Product Shelf Life24 Months
Test SpeedWithin 15 minutes
Sample Volume3 Full drops
Package25 Tests/Box
Storage ConditionStore 2-30℃

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.

Main Components

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

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.


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