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Antibodies.
Product News

Revvity’s EUROIMMUN Receives CE Mark for Novel Measles Antibody Detection Assay

Revvity, Inc. (NYSE: RVTY), announced the launch of EUROIMMUN’s CE-marked Anti-Measles Virus ELISA 2.0 (IgG) to support the diagnosis of a measles virus infection or to determine the immune status against measles virus.
A lateral flow test.
Product News

BIOHIT Introduces the FAEX™ Sample System for Stool Sample Collection and Handling

BIOHIT OYJ is excited to announce the launch of the BIOHIT FAEX Sample System, a stool sample collection and handling solution that can be seamlessly incorporated into any diagnostic workflow.
Someone with their hands outstretched, with a cartoon stomach hovering above.
Product News

Landmark Study at Homerton University Hospital Confirms GastroPanel®’s Diagnostic Accuracy

BIOHIT HealthCare is pleased to announce that a clinical study conducted by Homerton University Hospital NHS Foundation Trust, London, has confirmed the diagnostic accuracy of GastroPanel in identifying gastric cancer risk in patients.
Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select Panel.
Product News

Thermo Fisher Scientific Announces 510(k) Clearance of Molecular Clinical Test for SARS-CoV-2, Flu A, Flu B and RSV

Thermo Fisher Scientific has received 510(k) clearance from the U.S. Food & Drug Administration (FDA) for the Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select Panel.
DNA double helix structure.
Product News

PacBio and Radboud UMC Announce Remarkable Study Results Using HiFi Long Read Sequencing To Help Advance Rare Disease Diagnostics

PacBio (NASDAQ: PACB), announced a significant publication from Radboud University Medical Center (Radboudumc) and its research partners in the American Journal of Human Genetics.
Neurons that appear like cobwebs.
Product News

Spear Bio Secures FDA Breakthrough Device Designation for its Novel pTau 217 Blood Test, Advancing Scalable Solutions for Early Alzheimer's Disease Diagnosis

Spear Bio Inc., announced that its pTau 217 blood test has been granted Breakthrough Device Designation by the U.S. Food and Drug Administration (FDA).
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