Thank you for visiting our booth at the 14th annual Zebrafish Disease Models Conference. Feel free to check out the additional resources we have shared on this page or browse our zebrafish genome editing services here.
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In vivo fluorescence detected in 7 and 14 days post-fertilization RedEfish. (A) mScarlet expression was unique to the olfactory pits (op) found in the RedEfish; however, some autofluorescence was detected in the pigment cells surrounding the eyes (e) in all embryos. (B) mScarlet expression was identified in the digestive tract, specifically the liver (as indicated by *). (C) More punctate expression was observed in the anterior gut region (ventral embryo positioning). (D) Punctate expression was observed also in the tail fin (as indicated by *). (E) By 14 dpf, mScarlet expression was identified in the caudal vertebrae and dorsal root ganglia (drg) and was detected in the caudal vein plexus (cpv). Some autofluorescence was noted in both RedEfish and Casper larvae.
Additional Resources
Not ready to commit yet? Check out these additional resources to learn more about our zebrafish services or to learn some zebrafish genome editing tips and tricks from our experts.
- HELio Ortholog Gene Finder
- Generation of the Polycistronic mScarlet: GSG-T2A: Ttpa Zebrafish Line
- Zebrafish Genome Editing: CRISPR vs. Tol2
- Zebrafish Injection Mix: Buy verses DIY, what are the real costs?
- 11 Steps to a Successful CRISPR Knock-in
- Modeling Human Diseases in Zebrafish
- The Challenge of Getting CRISPR-based Knock-ins to Work in Zebrafish
- 6 Things That Can Go Wrong While Making Your Zebrafish CRISPR Knock-In
- To Truly Validate Your sgRNAs, Go In Vivo