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ISO13485 Rapid Neutralizing Antibody Test Kit 95.00% Acuracy

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.

ISO13485 Rapid Neutralizing Antibody Test Kit 95.00% Acuracy

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

Rapid Test Kit Neutralizing Antibody Rapid Test Kit High Quality Detection Rapid Antibody Test Kit

 

Intended Use

  • The Labnovation's SARS-CoV-2 neutralizing antibody rapid test kit is intended for the semi-quantitative determination of neutralizing antibodies to SARS-CoV-2 in human serum, plasma, fingersitick whole blood or venous whole blood specimens.
  • The test is intended use as an aid in identifying individuals with an adaptive immune response to SARS-COV-2, indicating recent or prior infection or assisting in evaluating the effectiveness of the vaccine clinical trials and mass vaccination.
  • Results are for the detection of total neutralizing antibodies to SARS-COV-2. Antibodies to SARS-COV-2 are generally detectable in blood several days after initial infection.

Specifications

Test ItemNeutralizing Antibody Test Kit
NumberLX-401701
Specificity98.00%
Sensitivity97.67%
Total Acuracy> 95.00%
Humidity35%-60%
Storage Temperature2-30°C
Sample TypeWhole bloo, Serum, Plasma
Sample VolumeWhole blood 20µL, Serum/Plasma 10µL
Package20 Tests/Kit
nspection MethodImmunochromatography
Shelf Life18 Months
TypeIVD Antibody Rapid Test
ApplicationFor Professional Testing Use

Main Components

  • 20 Test cassettes
  • 20 Disposable pipettes
  • 20 Sterile Safety Lancets
  • 1 Sample Buffer
  • 1 Colorimetric chart
  • 1 Instruction for use

Product Feature

  • Fast Test, get antigen test result within 10-15 minutes.
  • High sensitivity and specificity
  • Easy to operate, no need equipment, convenient and fast
  • Require little Specimens

Advantage

  • It can not only screen in the window period of infection oneset but also indicate the previous infection and reduce the rate of missed diagnosis
  • Blood sample detection , simple samplig, simple operation
  • Combined with nucleic acid kit to improve the screening rate of suspected patients
  • Rapid screening within 10-15minutes, resukts effective for 15minutes
  • Single detection, visual interpretation, no equipment, to adapt to the community
  • Easy operation, compatible with different samples
  • Room temperature storage

 

Notic

  • Sample should be human serum, plasma and whole blood only, other body fluid samples are not tested and may cause incorrect or inaccurate results.
  • All reagents have to be brought to room temperature (18 to 25 °C) before performing the test.

Use Step

  • Place the lanceton the test site.
  • Push down the lancet.
  • Collect the bloodby transfer pipette.

  • Add one drop of blood into the sample well.
  • Add 1-2 drops (30-60µL) of sample buffer into the sample well innediately.
  • Wait 15 minutes then read the result.

 

Interpretation of results

  • POSITIVE: The T line and C line are both displayed within the reaction window, indicates the neutralizing antibodies to SARS-COV-2 are detected. The result is positive.
  • NEGATIVE:The C line is displayed within the reaction window only, indicates absence of neutralizing antibody to SARS-COV-2.The result is negative..
  • INVALID:1. If the control (C) line is not displayed in 15 min, regardless of whether T line is present, the test result is invalid. It is recommended that the specimen should be re-tested.
    The test result is invalid after 20 min.

LIMITATIONS

  • The test is for in vitro diagnostic use only.
  • This test is designed for semi-quantitative detection of SARS-COV-2 neutralizing antibodies.
  • It is unknown at this time if the presence of antibodies to SARS-COV-2 confers immunity to re-infection. Consider other information including clinical history and local disease prevalence, in assessing the need for a second but different serology test to confirm an immune response.
  • The test results of this kit are for clinical reference only, and should not be used as the sole basis, and should be combined with other test methods, as live virus and pseudovirus neutralizing antibodies assay.

Application

  • Hospitals
  • Enterprise
  • School
  • Community
  • Family

FAQ

 

  • MOQ:

We have the MOQ limit,which is 10000 pieces.

  • Delivery date:

After order confirmed,we will arrange your order immediately,and offer you an
estimated delivery date.

  • Payment Method:

Business to business account.

  • Shipment:

We choose Air cargo or Ocean cargo.

  • Trade Company or Manufacturer:

Manufacturer

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