“After several unsuccessful gene targeting in mouse embryonic stem cells, using traditional methods and also CRISPR/Cas9, we approached CCP Transgenic Unit to help us to create a mouse model with single nucleotide exchange in the gene of our interest. They created the strategy, optimized conditions, injected mice and in four months we received first chimeras and in few weeks got germ line transmission. For very reasonable price. Perfect!”

“My research group has been in close contact with CCP for more than 5 years. Their excellent assistance with the mouse models has been essential for several high profile studies we have published in the last two years. Currently, we are analyzing together novel mouse knockout strains with the exciting phenotype. I very much appreciate CCP expertise in the phenotyping of both embryonic as well as adult mice. We would not be able to get that far without their help.”

“I was most impressed by the professionalism, cooperativeness, efficacy and technical competence of the CCP staff. Thanks to their expertise and cutting-edge technologies for constructing knock-out and transgenic mice, their skill in phenotyping technologies and scientific insight, our collaborations at CCP enabled us to move our projects a new level of scientific relevance. It is a real pleasure to have such a supportive and invaluable expert partner involved in your work.”

“We closely collaborate with the CCP for over four years and we have had only the best experience. Together we generated multiple mouse models of inducible and tissue-specific mitochondrial deficiency, which took our research to a whole new level. Everyone at the CCP has always been very helpful whenever we needed advice or practical help. We are happy to have the opportunity to work together and we plan new challenging projects for the future.”

“We established a collaboration with the CCP for a knock-out mouse model. They are highly professional and cooperative and offer a wide range of detailed analyses that have enriched the quality of our project. In our case, the gene they deleted is a noncoding RNA (ncRNA), and although the functionality of this class of genes is poorly characterized and their phenotypic analyses can lead to non-canonical outputs, they immediately join this challenging project with dedication and carefulness. We also had the opportunity to visit the institute, and we were positively impressed to see such a fully equipped facility. Highly recommended!”