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Alzheimer's Disease Preclinical CRO Solutions for Drug Discovery
Tackle the complex challenges of Alzheimer's Disease with Cyagen's integrated research platform. We combine validated animal models, end-to-end CRO services, and expert-led strategy to accelerate the discovery of new AD therapeutics for scientists worldwide.
An Integrated Approach to AD Research & Its Challenges

Alzheimer's is the world's leading neurodegenerative disease, with a severe epidemiological outlook and vast unmet medical needs. While progress has been made in understanding key pathogenic mechanisms like Aβ plaques, tauopathy, and neuroinflammation, preclinical research still faces critical bottlenecks, including poor clinical translatability of models and a lack of standardized efficacy evaluation criteria.

To address these complex challenges, Cyagen has developed a powerful and integrated research platform. Our portfolio of specialized animal models, combined with comprehensive in vivo and in vitro services detailed below, provides the critical tools scientists need to overcome these hurdles and accelerate their discovery programs.
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Cyagen offers a comprehensive portfolio of Alzheimer’s disease research models and services, spanning ready-to-use and custom mouse models, AAV-induced disease modeling, and disease-relevant cell products. Integrated in vivo, in vitro, and ex vivo capabilities support mechanistic research, target validation, biomarker analysis, and preclinical therapeutic evaluation. 

Disease-Relevant Induced Alzheimer's Disease Animal Models

Model Name Key Mechanism Application Action
AAV-induced Alzheimer's Disease (AD) mouse model Bilateral hippocampal injection of AAV vectors expressing mutant human APP and PSEN1 in C57BL/6J mice. Alzheimer's Disease View More

Relevant Model

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Disease-Relevant Cell Lines for AD Research

Cyagen offers gene-edited human iPSC lines and differentiated neural cell models carrying key Alzheimer’s disease-associated genes and mutations. These disease-relevant cell models support mechanistic studies, target validation, and in vitro therapeutic evaluation across multiple aspects of AD pathology.
Catalog No Parental cell Cell line Genetic Modification Application Species
SY-iKO-00003 iPSC KO-iPSC-APOE APOE knockout AD Human
SY-iKI-00003 iPSC KI-iPSC-NEUROG2 NEUROG2 knock-in at the AAVS1 locus AD Human
SY-iKI-00002 iPSC KI-iPSC-NEUROG2-PSEN1 ΔE9 PSEN1 ΔE9 knock-in at the AAVS1 locus AD Human
SY-iMU-00013 iPSC MU-iPSC-APOE4 (p.C130R) APOE point mutation (p.C130R) AD Human
SY-iMU-00014 iPSC MU-iPSC-APP-Swedish (p.K670N, p.M671L) APP Swedish mutation (p.K670N, p.M671L) AD Human
SY-iMU-00021 iPSC MU-iPSC-APOE (p.R154S) APOE point mutation (p.R154S) AD Human
SY-iMU-00023 iPSC MU-iPSC-PSEN1 (p.M146L) PSEN1 point mutation (p.M146I) AD Human
SY-iMU-00033 iPSC MU-iPSC-APP (p.E693Q) APP point mutation (p.E693Q) AD Human
SY-iMU-00020 iPSC MU-iPSC-TREM2 (p.R62H) TREM2 point mutation (p.R62H) AD Human
SY-iMU-00001 iPSC MU-iPSC-TARDBP (p.M337V) TARDBP point mutation (p.M337V) ALS/FTD/AD Human
SY-MU-00031 HT-22 MU-HT22-App (p.K595N, p.M596L) App (p.K595N, p.M596L) AD Mouse
SY-iN-00001 iPSC iPSC-NPC (Neural progenitor cells) — Neurology Human
SY-iCN-00001 iPSC iPSC-CN (Cortical neurons) — AD Human
SY-iAS-00001 iPSC iPSC-AS (Astrocytes) — AD Human
SY-iMG-00001 iPSC iPSC-Microglia — AD/PD/ALS Human
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Precision Drug Administration

Our team of skilled specialists is highly experienced in precision injection methodologies tailored for CNS research. We offer a comprehensive array of validated administration routes to ensure accurate and reliable delivery of your therapeutic candidates.
  • Systemic Delivery: Intravenous (tail vein), Intraperitoneal, Subcutaneous, etc.
  • CNS-Targeted Delivery: Stereotactic brain injection, Intrathecal injection, Intraventricular injection, and Intranasal administration.

Featured Technique: Stereotactic Brain Injection

Our stereotactic injection service enables targeted delivery to specific brain regions critical to AD pathology, such as the hippocampus and cortex, guided by 3D coordinates and verified through histological imaging.
Case Study: AAV Delivery to the CNS
Agent: AAV9-CMV-EGFP-HGH
Coordinates: -2mm, ±1.8mm, -1.5mm
Titer: 1.98×10¹⁴ vg/mL
Dose: 1×10¹⁰ vg/0.5μL/site
Imaging Time: 4 weeks post-injection
Figure: Precise injection site visualization using the brain stereotactic instrument.
Case Study: LPS-Induced Neuroinflammation Model
Agent: Lipopolysaccharide
Coordinates: +4.8mm, ±1.8mm, -8.0mm
Dose: 4μL/site (5 mg/mL)
Observation Time: 2 weeks post-injection
Observation: Rat displaying unidirectional rotational movement 14 days post-operation.
Figure: Significant behavioral changes observed 2 weeks post-injection.

Neurobehavioral Assessment for AD

We provide a focused suite of behavioral paradigms essential for evaluating the core cognitive and functional deficits associated with Alzheimer's Disease.
Behavioral Domain Recommended Tests for AD Research Function Tested
Learning & Memory Morris Water Maze Spatial learning and memory
Y-Maze Spatial working memory
Novel Object Recognition Recognition memory
Fear Conditioning Test Associative fear memory
Anxiety & Depression-like Behavior Elevated Plus Maze Anxiety-like behavior
Open Field Test Locomotor activity and anxiety
Motor Function & Coordination Rotarod Test Motor coordination, balance, and ataxia
General Well-being Nest Building Assessment of well-being and cognitive decline
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We offer a focused suite of analytical services to investigate the core pathological and molecular features of Parkinson's Disease, and to evaluate the efficacy of your therapeutic candidates.
Analysis Category Specific Services Key Applications & Targets in AD Research
Pathology & Biomarker Analysis Histology & Special Stains (H&E, Congo Red) Visualize general brain morphology and specifically identify dense-core amyloid plaques.
Immunohistochemistry (IHC) / Immunofluorescence (IF) Detect, localize, and quantify key pathological proteins directly in tissue sections (e.g., Aβ, p-Tau, Iba1 for microglia, GFAP for astrocytes).
ELISA & Immunoassays Accurately quantify levels of soluble/insoluble Aβ40/42, total Tau/p-Tau, and key inflammatory markers (e.g., cytokines) in brain tissue and plasma.
Gene & Protein Expression Western Blot Assess changes in protein levels and post-translational modifications (e.g., phosphorylation of Tau) for key biomarkers.
RT-PCR & qPCR Analyze the expression of target genes (e.g., APP, MAPT), inflammatory factors, and synaptic markers to understand mechanistic changes.
Physiological & Biochemical Analysis Biochemical Panels Assess the systemic impact of AD and therapeutic interventions by analyzing immune factors, antioxidant status, blood glucose, and lipid profiles.
Metabolic Testing (ITT, GTT) Evaluate metabolic dysregulation, a known comorbidity and potential driver of AD pathology.

AAV-induced Alzheimer's Disease (AD) mouse model

Model Validation Case Studies

Why Partner with Cyagen?
Comprehensive Model Solutions
Access a portfolio of ready-to-use, validated models and leverage our deep expertise in developing custom models on classic AD backgrounds.
Integrated Efficacy Platform
Utilize our one-stop, standardized services, from in-life behavioral studies to terminal molecular pathology.
Data-Driven Decision Support
Rely on our stringent quality control and commitment to reproducibility to deliver reliable data that supports your critical project decisions.
Expert-Led Study Design
Collaborate with our team of senior scientists to receive end-to-end support, from model selection to customized experimental protocol design.
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Global Antibody Drug Industry Development BlueBook (Frost & Sullivan)
Key Insights
The industry is undergoing a rapid transformation driven by next-generation modalities, globalized markets, and upstream technological innovations.
  • Market Structural Shift: Monoclonal antibodies drive steady growth, but ADCs and bispecifics are rapidly accelerating, reshaping the market with higher-value innovations.
  • Chinese Market Globalization: China is actively expanding globally, evidenced by a surge in high-value cross-border license-out deals.
  • Technology-Driven Efficiency: Advanced discovery engines—exemplified by Cyagen's HUGO-Ab platform and AI algorithms—are streamlining candidate screening, optimizing molecular design, and localizing the upstream supply chain.
  • Oncology-Focused Innovation: R&D pipelines remain heavily concentrated on high-incidence malignancies like non-small cell lung cancer, utilizing complex modalities to combat clinical resistance.
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