Ambryon

Validated AAV vector designs for in vivo CRISPR gene editing. Includes hfCas12Max, SaCas9, and CasMINI with customizable promoters and guide RNAs optimized for AAV packaging constraints.

Compact RNA-guided CRISPR nucleases for in vivo genome editing, including SaCas9 and CasMINI, with AAV-compatible reference designs.

Highly referenced CRISPR plasmids for genome editing research

Fluorescent and luciferase reporters and control vectors for AAV, lentiviral, and transfection platforms.

Curated collection of adenine and cytosine base editors for precise single-nucleotide editing without double-strand breaks