
Xerra: 3D automation and ease of use for animal model characterization
The ability to engineer mouse models that represent human disease is a valuable tool used by research groups around the world to better understand the biology of disease and drug targeting characteristics. A gap in sensitivity and resolution between in vivo and ex vivo techniques may make it hard to characterize an animal model. Using Cryo-Fluorescence Tomography (CFT), researchers can now obtain a 3D rendering of their mouse model to precisely understand the anatomical location of their genes of interest.
CFT
– as high-res as it gets
Fluoro-tagged adeno-associated viruses (AAVs) are used to deliver genes to mammalian cells and express fluorescent marker proteins in animals. Cryo-fluorescence tomography (CFT) quantifies this fluorescence, and differentiates different AAV strains, across the whole animal.
AAV liver markers
In this experiment, rats were treated with AAV9-GFP and observed 4 weeks later. Fluorescence was seen only in the liver. White light imaging (left panel) showed the location to the liver. Using CFT, a fluorescent protein marker was detected (middle panel) and localized to the liver (right panel). Software analysis allowed the fluorescent marker to be quantified.
