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GeneArt® Precision TALs

Precise, efficient gene sequence targeting and modification technologies

From precision genome editing and gene modification technologies to high-efficiency delivery systems, we have developed a broad range of solutions to help you create the modified genes, expression systems, and stable cell lines you need for your research—from culturing cells to modification, detection, and analysis. Our technologies—including GeneArt® TALs and CRISPRs—enable you to reliably modify genomic sequences and analyze the phenotypic outcomes. In addition, we can deploy a combination of advanced technologies to produce a custom construct or cell line that meets your specifications. Balancing performance and cost, our cell engineering portfolio is built on 20 years of industry-leading innovation and can grow with your research needs.

Which technology is right for you?   Request our new Genome Editing eBook  

Featured Technologies

Precise and flexible editing; targeting to any gene in any cell, with all-around freedom.

Perform siRNA- or miRNA-mediated loss-of-function analysis in eukaryotic systems.

Generate isogenic cell lines in your preferred cell background in much less time compared to traditional methods.

Rapid and efficient editing with multiplexing capabilities.

Create single-copy isogenic cell lines using Flp recombinase–based vectors and parental cell lines containing stably integrated Flp recombination target (FRT) sites.

Essential tools for monitoring the efficiency of your genome editing experiments.

Featured Applications


Tools for plant genome editing, cloning, DNA assembly, amplification, and analysis, plus Agrobacterium tumefaciens LBA4404 for transformation.


Modify and study gene and protein expression, and explore disease and differentiation pathways, using a variety of gene delivery techniques.


Allow us to generate high-performance cell lines with stable expression of your gene using a combination of our advanced technologies.

Technical resources