Authors
Marcia Brady
Summary
CRISPR/Cas9 gene editing technology brings a DNA editing revolution, which is faster, more accurate, less cost and has a wide range of potential applications than previous DNA editing techniques. Geneticists and medical researchers can use CRISPR/Cas9 technology to quickly delete, insert, or alter a portion of a DNA sequence. Guided by gRNA, Cas9 targets specific sites in the DNA and forms a double-stranded break (DSB). During DSB repair, one or more genetic changes are introduced through the non-homologous end joining (NHEJ) or homology directed repair (HDR, repair template required) pathway.
Introduction
CRISPR Platform, one of the leading gene editing technology companies, is specializing in CRISPR/Cas9 gene editing services. Based on our professional scientists' team and national-class labs, we have been successfully implemented hundreds of genes deletion in cells and mice using CRISPR/Cas9 technology. We use optimized gene targeting strategies to achieve the most efficient gene editing efficiency, and we provide you with one-stop gene editing services, including designing gene editing strategies for the final cell line or model animal. To meet your research needs, we offer CRISPR/cas9 knockout, knock-in, point mutation, conditional knockout cell lines and animal models, etc.
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