SARS-CoV-2 Antigen Detection Kit

  1. 15 mins for result, easy to use
  2. Results more quickly than RT-PCR tests
  3. Overall coincidence rate is 98.6%
  4. Used in hospital, pharmacy, custom border, hotel, school or other places.
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Description

Product Name: SARS-CoV-2 Antigen Detection Kit (Colloidal Gold Immunochromatographic Assay)

  • 1.1 Package specification 10, 20, 40 tests/kit
  • 1.2 Kit Composition

Kit compositions & Components

  • Test Card / Colloidal gold-labeled SARS-CoV-2 N protein antibody; SARS-CoV-2 N protein antibody and goat anti-mouse IgG polyclonal antibody coated on NC membrane
  • Sample extraction solution / Pbs Buffer
  • Sample extraction tube

Package specification

  • 2.5 mL × 2/kit (10 tests/ kits / 10 vials)
  • 2.5 mL × 4/kit (20 tests / kits / 20 vials)
  • 2.5 mL × 8/kit (40 tests / kits / 40 vials)

Performance indicators

  • 2.1 Appearance

The outer package is intact, with no damage or contamination, and the label is clear and legible.

  • 2.2 Net content

The net content of sample extraction solution should be no less than the labeled value.

  • 2.3 Strip width

The strip width should be no less than 2.5 mm.

  • 2.4 Liquid migration speed

The liquid migration speed should be no less than 10 mm/min.

  • 2.5 Coincidence rate of negative reference

The in-house negative reference is detected, and the negative coincidence rate should be 100%.

  • 2.6 Coincidence rate of positive reference

The in-house positive reference is detected, and the positive coincidence rate should be 100%.

  • 2.7 Precision

The in-house precision reference is detected and the result should be positive, with uniform chromaticity.

  • 2.8 Limit of detection (LOD)

The in-house LOD references are detected, the results of L1 and L2 should be positive and the result of L3 should be negative.

  • 2.9 Stability

The original packaging should be stored at 2°C-30°C in a dark and dry place, and the shelf life is tentatively 12 months. Items 2.1-2.8 should be detected respectively within 3 months after the expiration of the original packaging reagent, and the results should meet the requirements of each test item.

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