Eve Technologies is offering early access to the Human MSD® Discovery Assay® Neurodegeneration 7-Plex Array, enabling simultaneous measurement of seven biomarkers associated with Alzheimer’s disease, Parkinson’s disease, and other neurodegenerative disorders.
This new multiplex assay combines biomarkers of amyloid and tau pathology, neuroaxonal injury, astrocytic activation, and proteins involved in neurodegenerative disease processes. Researchers can investigate multiple aspects of neurodegeneration from a single sample using the ultrasensitive Meso Scale Discovery® (MSD®) platform.
GFAP | NfL | pTau217 | Aβ40 | Aβ42 | LRRK2 | TDP-43
$169.97 per sample | Starting from 50 μL | No minimum sample requirement
For Research Use Only. Not for use in diagnostic procedures.
Neurodegenerative diseases involve complex and often overlapping biological processes. While individual biomarkers provide valuable information, combining complementary targets can help researchers explore different aspects of disease biology within the same study.
The new Human MSD® Neurodegeneration 7-Plex Array brings together seven biomarkers in a single multiplex immunoassay, providing a broader approach to neurodegeneration research.
By measuring GFAP, NfL, pTau217, Aβ40, Aβ42, LRRK2, and TDP-43 simultaneously, researchers can investigate relationships between multiple biomarker pathways while conserving valuable sample material.
The Neurodegeneration 7-Plex Array combines established research biomarkers with emerging targets of interest in neurodegenerative disease research.
| Biomarker | Biological Relevance | Research Applications |
|---|---|---|
| GFAP – Glial Fibrillary Acidic Protein | A protein associated with astrocytes and astrocytic activation. | Alzheimer’s disease, neuroinflammation, glial responses, and neurodegeneration |
| NfL – Neurofilament Light Chain | A structural neuronal protein released during neuroaxonal injury. | Neurodegenerative disease progression, neuronal injury, and longitudinal biomarker studies |
| pTau217 – Phosphorylated Tau 217 | A phosphorylated form of tau strongly associated with Alzheimer’s disease-related pathology. | Alzheimer’s disease, tau-related pathology, and biomarker discovery |
| Aβ40 – Amyloid Beta 40 | An amyloid-beta peptide frequently studied alongside Aβ42 to investigate amyloid biology. | Alzheimer’s disease, amyloid metabolism, and Aβ42/Aβ40 research |
| Aβ42 – Amyloid Beta 42 | An aggregation-prone amyloid-beta peptide associated with amyloid plaque pathology. | Alzheimer’s disease, amyloid accumulation, and neurodegenerative disease biology |
| LRRK2 – Leucine-Rich Repeat Kinase 2 | A kinase involved in cellular signaling and lysosomal processes, with genetic and biological links to Parkinson’s disease. | Parkinson’s disease, LRRK2-associated pathways, and neurodegenerative mechanisms |
| TDP-43 – TAR DNA-Binding Protein 43 | An RNA-binding protein implicated in neurodegenerative proteinopathies. | ALS, frontotemporal dementia, LATE, and TDP-43-related neurodegeneration |
Together, these seven biomarkers provide opportunities to investigate multiple biological processes, including amyloid and tau pathology, neuronal injury, astrocytic responses, and disease-associated protein pathways.
Alzheimer’s disease research increasingly incorporates multiple biomarkers to investigate different aspects of disease pathology.
The combination of pTau217, Aβ40, Aβ42, GFAP, and NfL enables researchers to explore amyloid- and tau-associated changes alongside markers of astrocytic activation and neuroaxonal injury.
The inclusion of TDP-43 also provides an additional research target of interest for investigating overlapping neurodegenerative pathology and age-related dementia.
LRRK2 is an important area of investigation in Parkinson’s disease, particularly in studies of genetic susceptibility, kinase signaling, and lysosomal biology.
By combining LRRK2 with biomarkers such as NfL and GFAP, the panel supports research investigating relationships between Parkinson’s disease-associated pathways, neuronal injury, and glial responses.
TDP-43 plays a central role in the pathology of most amyotrophic lateral sclerosis (ALS) cases and many forms of frontotemporal lobar degeneration.
The inclusion of TDP-43 alongside NfL and GFAP creates opportunities for exploratory biomarker studies involving neuroaxonal injury, glial responses, and TDP-43-associated disease processes.
| Specification | Details |
|---|---|
| Assay Name | Human MSD® Discovery Assay® Neurodegeneration 7-Plex Array |
| Assay Code | MSDND7 |
| Technology | Meso Scale Discovery® (MSD®) Electrochemiluminescence |
| Format | Multiplex immunoassay |
| Biomarkers | GFAP, NfL, pTau217, Aβ40, Aβ42, LRRK2, TDP-43 |
| Sample Volume – Single Analysis | 50 μL |
| Sample Volume – Duplicate Analysis | 75 μL |
| Price | $169.97 per sample (single analysis) |
| Minimum Sample Requirement | No minimum sample count |
| Intended Use | Research Use Only (RUO) |
| Availability | Early Access |
Sample compatibility: Contact our scientific team to confirm the suitability of your sample matrix and project requirements before submitting samples.
Eve Technologies provides biomarker testing services to researchers worldwide, supporting projects ranging from initial exploratory studies to large-scale research programs.
With more than 20 years in operation and experience supporting research across academic, biotechnology, and pharmaceutical settings, our laboratory helps researchers access specialized immunoassay testing without the need to establish these workflows in-house.
Our Discovery Assays service offers:
Whether you are planning a pilot study, investigating new biomarker combinations, or expanding an existing neurodegeneration research project, our team can help you explore the available testing options.
The Human MSD® Neurodegeneration 7-Plex Array is a multiplex immunoassay offered by Eve Technologies that simultaneously measures seven neurodegeneration-related biomarkers: GFAP, NfL, pTau217, Aβ40, Aβ42, LRRK2, and TDP-43. It uses the ultrasensitive MSD® electrochemiluminescence platform and is available for research use.
The panel includes glial fibrillary acidic protein (GFAP), neurofilament light chain (NfL), phosphorylated tau 217 (pTau217), amyloid beta 40 (Aβ40), amyloid beta 42 (Aβ42), leucine-rich repeat kinase 2 (LRRK2), and TAR DNA-binding protein 43 (TDP-43).
The biomarker combination is relevant to research investigating Alzheimer’s disease, Parkinson’s disease, ALS, frontotemporal dementia, and other neurodegenerative conditions. Its individual markers are associated with different disease processes, making the panel useful for exploratory research into overlapping biological pathways.
The assay is intended for research use and is not a clinical diagnostic test.
Yes. The panel contains several commonly studied Alzheimer’s disease-related biomarkers, including pTau217, Aβ40, Aβ42, GFAP, and NfL. It also includes TDP-43, which is of research interest in overlapping neurodegenerative pathology.
Yes. Both amyloid beta 40 and amyloid beta 42 are included, allowing both analytes to be measured within the same multiplex panel. Researchers interested in calculating an Aβ42/Aβ40 ratio should confirm analytical suitability for their sample type and intended analysis.
The listed sample requirements are 50 μL for single analysis and 75 μL for duplicate analysis. Contact our team to confirm any additional sample preparation or matrix-specific requirements.
No. Eve Technologies’ Discovery Assays operate on a flexible pay-per-sample basis, allowing researchers to submit small pilot projects or larger sample cohorts.
No. The Discovery Assays service is a laboratory testing service, and researchers pay for the individual samples submitted for analysis.
Yes. Eve Technologies currently offers early access to the Human MSD® Neurodegeneration 7-Plex Array. Researchers can review the assay details, request a quote, and submit an order through our website.