NULISA™ Assays for Neurology

Unlocking Neurological Diseases with
High-Sensitivity Protein Detection

The convergence of disease modifying therapies and high-sensitivity protein detection technologies is transforming neurology. These advancements promise earlier diagnoses, personalized treatment plans, and improved patient outcomes across a spectrum of CNS diseases.

NULISAseq Multiplex Panels

Multiplex analysis of biologically informed content with the highest-sensitivity and broadest dynamic range.

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NULISAseq CNS Disease Panel 120

Profile Biomarkers of CNS Disease at the Lowest Limit of Detection

The ONLY neurology panel with Brain-Derived Tau assays. Simultaneous analysis of 120 proteins from a single 25ul sample with fg/ml sensitivity empowers researchers to detect disease earlier and differentiate between clinically similar phenotypes.

NULISAseq Mouse Panel 120

Discover More Biology in preclinical models

With the largest multiplexed protein panel for mouse studies, researchers can comprehensively measure inflammation from precious small volume samples and maximize the information captured in basic research and preclinical studies.

NULISAqpcr Single-plex Assays

Ultra-high sensitivity measurement of your most informative biomarkers.
Detect important low abundance proteins with attomolar sensitivity (low fg/mL)

NEW!
BD-pTau217

In neurodegenerative conditions marked by Tau accumulation, protein sources may originate from either brain or peripheral tissues. For Alzheimer’s disease, when detecting pTau217 from blood or plasma it is critical to distinctly detect brain originated pTau217 versus that originated from peripheral tissues.

NfL

Elevated levels of Neurofilament light (NfL) can indicate the extent of neuronal injury and are useful for diagnosing and monitoring the progression of neurological diseases, such as Amyotrophic Lateral Sclerosis (ALS), Alzheimer’s Disease (AD), Multiple Sclerosis (MS), etc.

IL-1B

Coming Soon! Overproduction of Interleukin-1 beta (IL-1β) is associated with various inflammatory diseases, including rheumatoid arthritis, inflammatory bowel disease, and certain neurodegenerative disorders like Alzheimer's disease.

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Related Publications

Check out these selected publications demonstrating the superior performance of NULISA assays to detect critical cytokines and immune related biomarkers.

Hear from the Experts in Neurology

Advancing biomarker research for CNS Disease

  • Precision Biomarkers for Early Diagnosis
    Early diagnosis is key to effective intervention in CNS diseases. Biomarkers such as amyloid-β and tau proteins for Alzheimer’s Disease, α-synuclein for Parkinson’s Disease, and neurofilament light chain (NfL) for ALS, MS, and other conditions are transforming early detection capabilities. These markers enable clinicians to detect subtle pathological changes before the onset of clinical symptoms.
  • Fluid Biomarkers from Blood and Cerebrospinal Fluid (CSF)
    Traditionally, CSF has been the primary source for biomarker detection, but recent innovations have Blood-based biomarker detection reduces reliance on invasive procedures like lumbar punctures, improving patient compliance and accessibility. Plasma tau, NfL, and glial fibrillary acidic protein (GFAP) are emerging as reliable indicators for diseases like Alzheimer’s, FTD, and TBI, offering less invasive diagnostic options.
  • Biomarkers for Monitoring Disease Progression
    Dynamic biomarkers such as phosphorylated tau (p-tau) and NfL allow clinicians to track disease progression and treatment efficacy. Longitudinal tracking of biomarkers such as NfL provides valuable insights into disease progression in ALS, MS, and other neurodegenerative conditions.
  • Improved Therapeutic Development
    High-sensitivity detection accelerates drug development by identifying target engagement and treatment responses at early stages.

Key Therapeutic Areas

Alzheimer’s Disease (AD)

Biomarkers such as amyloid-β, p-tau, and total tau (t-tau) are critical for early detection and monitoring. High-sensitivity techniques enable the detection of these markers in plasma, making routine screening feasible.

Parkinson’s Disease (PD)

α-synuclein aggregates in CSF and blood are being explored as diagnostic and prognostic markers. High-sensitivity assays can distinguish subtle changes associated with early disease stages.

Amyotrophic Lateral Sclerosis (ALS)

NfL and other neurodegeneration-related proteins serve as reliable indicators of motor neuron injury. Their levels in blood and CSF correlate with disease progression and therapeutic response.

Multiple Sclerosis (MS)

NfL and GFAP are emerging as valuable biomarkers for assessing inflammatory and neurodegenerative processes in MS. High-sensitivity detection enhances the precision of these measurements.

Frontotemporal Dementia (FTD)

Genetic and protein biomarkers, including progranulin and tau, provide insights into FTD subtypes. Sensitive assays enable earlier differentiation from other dementias.

Traumatic Brain Injury (TBI)

Acute biomarkers like GFAP and ubiquitin C-terminal hydrolase L1 (UCH-L1) aid in diagnosing and prognosticating TBI severity. High-sensitivity detection ensures rapid and accurate evaluation in clinical settings.

FOR RESEARCH USE ONLY. Not for use in diagnostic procedures. 

Steve Williams, MD, PhD

CSO

Dr. Willams serves as the company’s Chief Scientific Officer. He was previously Chief Medical Officer at Standard Biotools and at SomaLogic where he pioneered the discipline for discovery and validation of predictive, diagnostic and prognostic models using machine-learning applied to large-plex proteomics. 20 such tests were used for drug characterization, safety and efficacy when incorporated in clinical drug trials at Pharma/Biotech and 17 different multivariate tests were validated and translated into regulated healthcare uses. Prior to SomaLogic, Dr. Williams was at Pfizer in the UK and the USA as a clinical triallist in Translational Medicine, and subsequently as VP, Global Clinical Technology. He sat on the National Advisory Council for the National Institute of Biomedical Imaging and Bioengineering, the Executive Committee for the FNIH Biomarkers Consortium, and worked with FDA and PhRMA on developing evidentiary standards for biomarker qualification. Dr. William’s medical training was in London, at Charing Cross and Westminster Medical School, followed by a PhD in medicine/physiology at the same institution and training in Radiology at the University of Newcastle Upon Tyne. Steve is co-inventor on 26 proteomics patents and author/coauthor on multiple foundational proteomics manuscripts.

Justin McAnear

CFO

Mr. McAnear serves as the company’s Chief Financial Officer. He brings over 25 years of operational and financial leadership experience across various sectors and was instrumental in taking 10x Genomics public in 2019, serving as its CFO for over five years. Mr. McAnear served for over 3 years as Tesla’s VP of Worldwide Finance and Operations, supporting landmark initiatives such as the Model X and Model 3 launches and Solar City acquisition.  He also held various roles at Apple and J&J earlier in his career and served as a naval officer and aviator for over 9 years.