Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent Kit / Reagent Kit Access® Antibody Test SARS-CoV-2 IgG For use with Access Family of Immunoassay Systems 200 Tests 20 µL Sample VolumeC58961
Picture of Reagent Kit Access® Antibody Test SARS-CoV-2 IgG For use with Access Family of Immunoassay Systems 200 Tests 20 µL Sample VolumeC58961

Reagent Kit Access® Antibody Test SARS-CoV-2 IgG For use with Access Family of Immunoassay Systems 200 Tests 20 µL Sample VolumeC58961

Reagent-Kit-Access®-Antibody-Test-SARS-CoV-2-IgG-For-use-with-Access-Family-of-Immunoassay-Systems-200-Tests-20-µL-Sample-VolumeC58961

SKU #

#1167489

MPN #

C58961

Brand

Beckman Coulter

Stock

In Stock

Quantity

100

Features

REAGENT, ACCESS SARS-COV-2 IGG(200TESTS/KT) D/S

$1,299.25 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1167489
Manufacturer # C58961
Brand Access®
Manufacturer Beckman Coulter
Application Reagent Kit
Container Type Well
For Use With For use with Access Family of Immunoassay Systems
Number of Tests 200 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Sample Type Serum / Plasma Sample
Storage Requirements Requires Refrigeration
Test Name SARS-CoV-2 IgG
Test Type Antibody Test
Time To Results 25 Minute Results
Type Chemiluminescent Immunoassay
UNSPSC Code 41116020
Volume 20 µL Sample Volume
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  • The Access SARS-CoV-2 IgG assay is only for use under the Food and Drug Administration's Emergency Use Authorization: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet requirements to perform moderate or high complexity tests
  • The Access SARS-CoV-2 IgG assay is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection; at this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
  • Negative results do not preclude acute SARS-CoV-2 infection; if acute infection is suspected, direct testing for SARS-CoV-2 is necessary
  • False positive results for the Access SARS-CoV-2 IgG assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • The Access SARS-CoV-2 IgG assay is designed to target antibodies against the coronavirus spike protein that may be more likely to confer immunity
  • The Access SARS-CoV-2 IgG assay can be run in random access mode, seamlessly integrating into current laboratory workflow without the need for batching or special maintenance
  • Time-to-first result (approx.): 25 minutes