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EAE (MOG-induced)

This article explains the "EAE (MOG-induced)" model, which is widely used in research and new drug development for multiple sclerosis (MS). We will summarize its characteristics, main uses, research subjects, and key products.

EAE (MOG-induced)

EAE isPathological model widely used to study multiple sclerosis (MS)In this model, immune cells are activated by injecting mice with MOG (myelin oligodendrocyte glycoprotein) peptide along with an immunostimulant. This causes the immune cells to attack their own nerves (myelin) and induce inflammation.

By using the EAE model,Clarifying the pathological mechanisms of multiple sclerosis, and evaluating the efficacy of new immunotherapies and anti-inflammatory drugs.This will be possible.

The main subjects of research utilization

Diseases for research How to use a disease model
Multiple Sclerosis (MS) Used for efficacy evaluation of new therapeutic agents and confirmation of neuroprotective effects
Optic neuritis To elucidate the mechanism of vision loss caused by inflammation and demyelination of the optic nerve, which is often associated with MS, and to evaluate drug efficacy for symptom relief.

EAE models are primarilyEvaluation of Novel Therapeutics for Central Nervous System Autoimmune Diseases Such as Multiple SclerosisIt is widely used. It is also widely used in basic research, such as elucidating the mechanisms by which autoreactive T cells cause inflammation and demyelination, and exploring new therapeutic targets.

How to use Details
Clinical scoring Quantitatively evaluate motor impairments such as reduced tail tension, hindlimb paralysis, and complete quadriplegia through daily scoring.
Histopathological analysis Create sections of the spinal cord and brain to evaluate the degree of inflammatory cell infiltration and demyelinated areas of myelin (myelin sheath).
Immunological analysis Measuring the dynamics of T cells, macrophages, etc. in the central nervous system and lymph nodes

EAE (MOG-induced) review

Demonstration of establishing a multiple sclerosis model using MOG peptide

In this paper,Confirmation of response to multiple sclerosis (MS)In the study, synthetic MOG peptide injections into H-2b mice (e.g., C57BL/6J) induced T cell responses similar to multiple sclerosis, causing severe and chronic neuropathology, including ascending paralysis.

Pathology varies depending on the mouse strain, indicating the importance of epitope specificity and self-reactive T cells in disease induction.

Reference: National Library of Medicine
https://pubmed.ncbi.nlm.nih.gov/7621871/

EAE (MOG-induced) Main Products

Here, we introduce two products from the top 10 Google search results for "EAE (MOG induction) products," specifically those on which product pages could be confirmed, listed in order of search ranking (as of June 4, 2026).

Multiple Sclerosis (EAE) Mouse Model

This is an autoimmune disease mouse model developed by Biosyngen for preclinical multiple sclerosis research.

Manufacturer/Distributor Analysis items Primary Endpoint
BioSiteGen Japan Co., Ltd. Weight measurement, clinical scores (motor function such as paralysis), and histopathological analysis (cellular infiltration by H&E staining, etc.) Improvement (decrease) in clinical score, suppression of weight loss, and reduction in infiltration of inflammatory cells and demyelination in spinal cord tissue.

Hooke Kit MOG35-55CFA Emulsion PTX

This kit is provided for efficient induction of EAE in mice. It includes an emulsion pre-mixed with MOG35-55 antigen and complete Freund's adjuvant (CFA), along with pertussis toxin (PTX).

Manufacturer/Distributor Analysis items Primary Endpoint
Manufacturer: Hooke Laboratories, Inc.
Distributor: Cosmo Bio Co., Ltd.
Clinical scores (decreased tail tone and hindlimb paralysis), body weight changes, histopathological assessment of central nervous system tissue, and immunological analysis Confirmation of EAE incidence, degree of motor dysfunction, lesion formation in the spinal cord

Summary

This article introduced information on the EAE (MOG-induced) model, which is used in multiple sclerosis research and new drug development.When conducting non-clinical studies, reliable model selection is important.This can be said. This site introduces pathological models used in preclinical studies, so please refer to the following articles as well.

3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories, Inc. has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories, Inc. is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • Labcorp Holdings Inc. provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • Labcorp Holdings Inc.’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio Co., Ltd.offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio Co., Ltd. provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio Co., Ltd. delivers unmatched analytical precision and consistency.

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