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Neuroscience

Discover Cisbio’s solutions, with kits and reagents dedicated to neuroscience research

It is reported that about 40 million people around the globe are living with Dementia, and this number is likely to at least double by 2050.The study of all the neurodegenerative disorders and the associated molecular pathway represents one of the greatest challenges faced by researchers today. In this dedicated webpage, you will discover solutions, methods, and contents to help you in your day to day research.

Guide
Guide

Discover the pathways involved in neuroinflammation and neurodegeneration

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Guide
Guide

Taking autophagy regulation research a step further

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Boost your research on Alzheimer’s disease

Neurodegenerative diseases have been correlated to proteinopathies, owing to the excessive accumulation of misfolded, hyperphosphorylated, and aggregated proteins. These protein inclusions within neurons represent the primary hallmarks of major disorders such as Tau and amyloid-β proteins in Alzheimer’s Disease.

Our company already provides a large selection of life science assays to quantify these valuable biomarkers that represent the key signatures of neurodegenerative diseases

Pathogenesis of Alzheimer’s Disease - amyotrophic lateral
Pathogenesis of Alzheimer’s Disease

Neuroscience guide

If you want to learn more and discover a large panel of molecular pathways involved in Alzheimer’s Disease progression and in other neurodegenerative diseases, download our neuroscience guide here.

Download your guide

Download your guide about neurodegenerative diseases and neuroinflammation pathways
Tau aggregation in Alzheimer’s disease pathogenesis addressed with HTRF assays

Literature review about Tau investigation

The propagation of the aggregate form of the TAU protein is known to be involved in the pathogenesis of several neuronal disorders, including Alzheimer’s Disease. This note groups recently published studies giving examples of the use of HTRF assays for TAU aggregation studies.

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Dive deeper into Parkinson’s disease

A characteristic of many neurodegenerative diseases is the dysfunction in protein homeostasis and/or the aggregation of some proteins. Protein inclusions within neurons represent the primary hallmark of the major disorders such as α-Synuclein in Parkinson’s Disease.
Protein aggregation is increasingly considered a late stage hallmark of the disease. The key challenge is to identify biomarkers that are detected early, well before symptoms appear.
Our goal is to develop assays to track dysfunctions in neuronal protein degradation involving autophagy and mitophagy mechanisms, as well as important markers of neuroinflammation, to tackle attractive targets and open new hopes for the identification of innovative treatments.

Pathogenesis of Parkinson’s Disease
Pathogenesis of Parkinson’s Disease
Detection of phospho, total and aggregated a-Synuclein
to characterize biological samples

Poster on alpha-synuclein investigation

Cisbio provides various solutions to measure Total α-Synuclein, phosphorylated α-Synuclein (S129), or aggregated a-Synuclein on variable samples for in vitro testing. Download the poster to discover how.

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Neuroscience guide

Neurodegenerative diseases such as Parkinson’s Disease occur as a result of neuroinflammation and neurodegenerative progression. For the moment, these diseases are incurable. However as research progresses, many similarities between these diseases have been found at a sub-cellular level. This guide provides you with an overview of the current knowledge on neuroinflammation and neurodegeneration.

Download your guide

Download your guide about neurodegenerative diseases and neuroinflammation pathways

Tackling ALS and FTD research with HTRF technology

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects the motor system and leads to progressive muscle weakness, including that of the respiratory system. Frontotemporal dementia (FTD) is a disease characterized by the degeneration of cortical neurons (frontal and temporal lobes) and basal ganglia, associated with a loss of cognitive functions as well as behavioral and personality changes.

Up to 50% of patients with ALS develop frontotemporal dysfunction, while 15% of patients with FTD develop motor neuron dysfunction. Despite distinctly different symptoms, ALS and FTD share significant overlaps at the molecular level.

Cisbio offers you several solutions and reagents to investigate FTD and ALS.

Amyotrophic Lateral Sclerosis and Frontotemporal Disease investigations
Amyotrophic Lateral Sclerosis and Frontotemporal Disease investigations

Neuroscience guide

Discover the emerging pathways involved in ALS and FTD. Benefit from this guide to get a better understanding of the molecular and cellular basis of neurodegenerative diseases.

Download your guide

Download your neuroscience guide

Cisbio’s offer on rare diseases

A characteristic of many neurodegenerative diseases, including rare diseases such as Spinal Muscular Atrophy and Friedreich’s ataxia, is a dysfunction in protein homeostasis and/or the aggregation of some proteins.

Cisbio has developed a panel of ready-to-use assays to monitor biomarkers involved in challenging neurodegenerative diseases.

Spinal muscular atrophy

Friedreich’s ataxia

Taking neuroinflammation research a step further

Chronic neuroinflammation and related innate immune responses triggered by microglial and astrocyte cells play a major role in the development of neurodegenerative diseases. Neuroinflammation mediated by glial cells (microglia & astrocytes) is recognized as an important mechanism regulating brain function and dysfunction, thus contributing to the onset of neurodegenerative diseases.

Cisbio offers a wide range of high-quality cytokine, chemokine, biomarker and phosphorylation assays to monitor neuroinflammatory processes.

In the absence of dysregulation, glial cells and the brain’s immune cells elicit protective mechanisms to locally and rapidly respond to defective neurons, injury, and to damaged cells or neuronal invasion. In a healthy context, neuroinflammation is transient and maintains homeostasis in the brain. However, a sustained inflammation and dysregulation of the microglial and astrocyte cells adversely impacts homeostasis in the brain, and has been shown to exacerbate disease progression.

glial cells and brain’s immune cells
Webinar  on neuroinflammation

Linking neuroinflammation and neurodegeneration

New discoveries recently showed the involvement of neuroinflammation in the progression of neurodegenerative diseases such as amyotrophic lateral sclerosis, Parkinson’s disease, and Alzheimer’s disease. Featuring two experts, Michael Heneka (MD, PhD) and Shane Liddelow (PhD), this free on-demand webinar aims to highlight the importance of neuroinflammation research.

Watch webinar

Literature review on neuroinflammation

Literature review on neuroinflammation

Pursuing the quest for better understanding of neuroinflammation processes has led to investigations into the pro- and anti-inflammatory balance triggered by microglia and astrocyte cell behavior. This literature review has gathered scientific publications and reports on the effective implementation of HTRF assays.

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Neuroscience guide

This neuroscience guide provides an overview on the current knowledge of neuroinflammation pathways, and details the contribution of glial cells to neurodegeneration.

Download your guide

Download your guide about neurodegenerative diseases and neuroinflammation pathways