We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us

Download Mobile App





New COVID-19 Antibody Assay Can Analyze Up to 40,000 Samples per Day Using Serum or Dried Blood

By LabMedica International staff writers
Posted on 24 Sep 2020
A new COVID-19 antibody assay can analyze up to 40,000 samples per day and is suitable for both serum and dried blood sampling.

The new COVID-19 antibody has been developed by LGC's Immunogenicity Centre of Excellence (Cambridge, UK) and uses serum or capillary blood collected remotely with the Mitra microsampling device from Neoteryx LLC (Torrance, CA, USA). More...
Individuals can be tested for SARS-CoV-2 antibodies by visiting a blood draw center to provide a serum sample via phlebotomy, or by collecting their own blood sample at home using the Mitra device and a simple fingerstick method. The Mitra blood samples can be posted through the regular mail to LGC's Centre of Excellence laboratory for testing, where sample data are processed and reported using the company's custom LIMS system. The assay developed by LGC for SARS-CoV-2 antibody testing achieves specificity of (95% CI) 100% (98.7-100.0) and sensitivity of (95% CI) 98.0% (87.0-99.0) for samples taken 21 days post positive PCR test. Sample results can be reported within 24 hours of sample receipt.

"A real value of remote blood sampling with the Mitra device for testing in LGC's outstanding lab is that people don't have to leave home to learn if they have developed SARS-CoV-2 antibodies," said James Rudge, PhD, Technical Director, Neoteryx. "Our Mitra is designed with volumetric absorptive microsampling, or VAMS technology, which enables virtually anyone to collect a few drops of blood on the device with scientific precision."

"Our assay is suitable for partnering with employers for back to work testing using the self-sampling Mitra device, and therefore does not require a phlebotomist to take the blood sample in a healthcare setting," added LGC's Commercial Director, Michael van der Merwe. "The assay can also support patient stratification for clinical trials and COVID-19 vaccine development. As well as qualitative data, we can also provide semi-quantitative data on the level of antibodies present indicating the magnitude of the immune response."

Related Links:
LGC's Immunogenicity Centre of Excellence
Neoteryx LLC



Platinum Member
Fully Automatic ACLIA Analyzer
MAGLUMI X8
Gold Member
SARS-CoV-2 PCR Test
Macurra SARS-CoV-2 PCR Kit
New
Gold Member
Platelet Function Analyzer
PL-12
Japanese Encephalitis Test
Japanese Encephalitis Virus Real Time PCR Kit
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: Graphical abstract (Pola, I., Akinyemi, T., Tan, K. et al. Nature Communications(2026). https://doi.org/10.1038/s41467-026-74971-4)

Blood Biomarker Study Reveals Population-Specific Differences in Alzheimer’s Disease

Blood-based biomarkers are emerging as tools for detecting Alzheimer’s disease–related changes without relying on advanced brain imaging or cerebrospinal fluid (CSF) analysis. However, much of the foundational... Read more

Molecular Diagnostics

view channel
Image Credit: Shutterstock

Blood Test for Lung Cancer Screening Receives FDA Breakthrough Device Designation

Lung cancer remains the leading cause of cancer death in the United States, yet only about 18% of people eligible for screening undergo low-dose computed tomography, the current guideline-recommended method.... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.