Customized genome editing services using CRISPR/Cas9 technology for SNP replacement, large reporter gene knock-in, and DNA knock-out in iPSC and other cell lines.
We Accelerate your research with our comprehensive genome editing services. Our expert team utilizes CRISPR/Cas9 technology to tailor genome editing to your specific requirements. Whether you require permanent knock-out, conditional knock-out, point mutation, or insertion, we have you covered.
Our services are compatible with both in-house iPSC lines and custom-provided cell lines. If you choose cell lines derived from patients, rest assured that they have undergone thorough testing for Mycoplasma, HIV, Hepatitis B, and C, ensuring their quality and safety.
We offer efficient and effortless end-to-end services. We handle cell reprogramming and gene editing, allowing you to focus on your research while we optimize the process, taking the burden off your shoulders.
We offer a range of ready-to-use CRISPR-engineered cells for various disease models.
Established differentiation and marker staining protocols for a wide range of cell types, ensuring reliable and consistent results every time.
Drug discovery, drug screening, disease modeling, personalized medicine, and preclinical cell regeneration projects. Our approach allows us to develop tailored solutions that address your unique needs and accelerate the path to success.
Customized cell isolation services with an extensive network of ethically procured tissues from donors with specific requirements. Available in a variety of formats and can be obtained from a wide range of species and diseases.
It takes 2-5 months depending on the recovery of the cells provided by the customer, the proliferation rate and transfection efficiency of the cells, and validation assays requested by the customer.
We will ship 3 frozen vials of each clone to the customer. Live cultures are available upon requests. We will also provide final report in publication-ready format.
We will provide 1) the gene editing method we used to edit the cell line; 2) the recovery and maintenance method after you receive the cells; 3) Cell recovery and live culture delivery if desired; 4) in-house training course if desired.