The ability to quickly install variant alleles in C. elegans and quantitatively measure the variant phenotypes provides researchers a path to rapidly address the consequence of gene variation for answering questions of disease biology.
We have preselected disease-relevant strains and validated their genetic identity with PCR and sequencing. These humanized model systems can serve as another efficient tool set to study human diseases.
Alzheimer’s Disease Panel
Strains carrying genetic mutations that are associated with Alzheimer’s disease, validated via PCR and sequencing.
Epilepsy Disorder Panel
Strains carrying genetic mutations that are associated with Epilepsy disorder, validated via PCR and sequencing.
