Cell Modification

Cell modification products, including gene editing tools, vectors, and transfection reagents, allow scientists to introduce genetic changes into cells to enhance their therapeutic potential. These modifications can improve cell efficacy, target specificity, and safety profiles. Gene editing, such as CRISPR-Cas9, enables precise alterations to correct genetic defects or engineer immune cells for cancer therapies. The use of vectors and transfection reagents facilitates the delivery of these genetic instructions into cells, enabling their successful modification. Cell modification is a cornerstone of next-generation therapies, offering customized treatment solutions for a range of diseases.