Confidence in Your Results
Our high-quality assays enable researchers to detect and quantify blood-based biomarkers for neurodegenerative diseases with the exceptional sensitivity and specificity you’ve come to expect from Beckman Coulter.
And our partnerships with world-class research centers facilitate a deeper understanding of biomarkers involved in conditions such as Alzheimer's disease.
Blood-based Neurology Disease Assays
| Assays for Research Use Only | IFU | Information Bulletin |
| BD-pTau 217 | Link | Link |
| p-Tau217 | Link | Link |
| GFAP | Link | Link |
| NfL | Link | Link |
| APOE ε4 | Link | Link |
| ß-AmyIoid 1-42 | Link | Link |
| BD-Tau | Link | Link |
| Research Use Only Assays in Development | ||
| MTBR-Tau (CSF) | ||
| TDP-43 | ||
| p‑Tau 205 | ||
For Research Use Only. Not for use in diagnostic procedures.
Advance Alzheimer's disease research with high-specificity detection of brain-derived pTau217
The high-specificity, automated Access BD-pTau217 RUO assay enables improved biological differentiation and supports disease staging in Alzheimer's disease research:
- Selectively detects brain-derived pTau217, reducing contribution from peripheral tau signal in plasma-based studies
- Supports research into disease staging, progression, and key inflection points
- Enables improved characterization and stratification of research populations, including complex or real-world cohorts
Explore analytical performance and assay design
Poster: A New High-Throughput, Fully Automated Immunoassay for Plasma Brain-Derived pTau217
For Research Use Only. Not for use in diagnostic procedures.
Fully Automated APOE ε4 Testing
Our newly available APOE ε4 RUO blood-based immunoassay offers >99% concordance with PCR genotyping—in only 20 minutes. While not
diagnostic, APOE ε4 status can provide insights into risk of developing Alzheimer’s disease.
“We are investing in our immunoassay technology to develop new, blood-based, high throughput, high sensitivity assays to detect and measure neurological biomarkers at a scale to address the growing global challenge."
Building on our legacy of innovation, we are advancing the future of diagnostics around the globe to deliver accurate,
affordable testing solutions at scale.
Request More Information About Neurology
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1. GBD 2019 Dementia Forecasting Collaborators. Estimation of the global prevalence of dementia in 2019 and forecasted prevalence in 2050: an analysis for the Global Burden of Disease Study 2019. Lancet Public Health. 2022;7(2):e105-e125.https://www.thelancet.com/journals/lanpub/article/PIIS2468-2667(21)00249-8/fulltext
2. World Health Organization. Parkinson disease. August 9, 2023. Accessed February 7, 2025. https://www.who.int/news-room/fact-sheets/detail/parkinson-disease
3. Guan B, Anderson DB, Chen L, Feng S, Zhou H. Global, regional and national burden of traumatic brain injury and spinal cord injury, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. BMJ Open. 2023;13(10):e075049. https://bmjopen.bmj.com/content/13/10/e075049
4. Walton C, King R, Rechtman L, et al. Rising prevalence of multiple sclerosis worldwide: Insights from the Atlas of MS, third edition. Mult Scler. 2020;26(14):1816-1821. https://pubmed.ncbi.nlm.nih.gov/33174475/"doi:10.1177/1352458520970841
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Educational Resources
p-Tau217 and Alzheimer’s disease
Plasma p-Tau217 levels have shown correlation with amyloid pathology, which has implications for identifying neurodegenerative diseases such as AD. Elevated levels of p-Tau217 can help distinguish AD from other forms of dementia.
Measuring p-Tau217 may help to further research into AD pathology and flag samples from those with early-stage AD pathology.
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