Gene editing or genome editing allows DNA to be added, removed, modified, or replaced at particular locations in the genome. The techniques could be used in various application areas, such as correcting specific genetic mutations in the human genome and preventing the spreads of diseases. Among the gene editing techniques, the Clustered Regularly Interspace Short Palindromic Repeats (CRISPR)/Cas9 is awarded the Nobel Prize in Chemistry 2020. CRISPR/Cas9 works as molecular scissors to make cuts in DNA at specific locations to change the genomes. This technique is faster, cheaper, more accurate and efficient than other existing genome editing methods. We provide the solution for establishing gene edited cell lines for research use. We can help you to design and construct the CRISPR/Cas9 plasmids, to package different types of virus, and then to do gene editing on your interested cell lines or microorganism. 

We are particularly interested in making reporter knock-in stem cells for research and drug discovery purpose. The stem cells carrying endogenous reporter can then been differentiated into more relevant cell models such as organoid.  Our platform for organoid engineering is being prepared now.

We have successfully modified the genome on many cell types including iPS cells and neural stem cells using CRISPR/Cas9 technology.  Our service is 100% guaranteed.  You can get money back if the gene editing is not successful.