Rare Disease Model Collaboration Program

As a leading provider of custom mouse and rat models, Cyagen aims to support the advancement of rare disease and related gene therapy research with our expertise. Cyagen ... Read More ›

Live KO/cKO Mice Shipped in 2 Weeks, only $1,299

Cyagen’s Weekly Flash Sales for Knockout Models will provide a list of specific gene knockout (KO) mice that are available until the ‘off-the-shelf date’ at a substantial discount. ... Read More ›

ACE2 Model Validation Report

In the wake of the COVID-19 pandemic, research teams around the globe are racing to develop vaccines and therapeutic options for the disease. Accurate animal models are essential ... Read More ›

Cyagen Ambassador Awards

Over the past 15 years, Cyagen has helped more than 3,000 university and company partners decipher the complexities of the genome in the most economical and accurate way. ... Read More ›

Grant Application Support Letter

To give your grant proposal a competitive edge, Cyagen's model generation experts can provide a letter of support that clearly outlines model generation strategies, budget, and timeline - ... Read More ›

Free Homozygous Breeding

Since the Cyagen Knockout Catalog Models repository was established, it has delivered ready-to-use heterozygous gene knockout (KO) mice to researchers worldwide in as fast as 3 months. In ... Read More ›

Advancing Neurodegenerative Disease Research with Animal Mod...

Population aging is one of the most important social health issues in the world today and will only increase in the future. With rising life expectancy and continually ... Read More ›

Knockout Mice - An Efficient Tool for Gene Function Research

Knockout mice have been essential for gaining proper understanding of gene function, studying human disease mechanisms, and accelerating drug development - playing an important role in biomedical advancements ... Read More ›

Rare Disease Research and Gene Therapy Resources List

As a leading provider of custom mouse and rat models, Cyagen aims to support the advancement of rare disease and related gene therapy research with our expertise. We ... Read More ›

The Pathogenic Gene of Huntington's disease – HTT

Huntington's disease (HD) is a rare, progressive brain disorder that is inherited in an autosomal dominant manner - this disorder is caused by a defective huntingtin (HTT) protein ... Read More ›

AAV-CRISPR/Cas9-Mediated Gene Editing - An Efficient Tool fo...

Familial hypercholesterolemia (FH) is characterized by elevated levels of low-density lipoprotein cholesterol (LDL-C) and premature cardiovascular disease (CVD). FH is an autosomal dominant genetic disease (with a gene ... Read More ›

Immunology and Inflammation Research - IL17A

Since IL17A plays an important role in infectious diseases, inflammatory, autoimmune diseases and cancer studies, IL17A has become a hot research target for many studies. In this Gene ... Read More ›