Creating and screening for SNPs

One of the most powerful applications of genome editing technology involves the introduction of single-nucleotide substitutions at specific genomic sites to mimic single-nucleotide polymorphisms (SNPs) implicated in human diseases or to introduce stop codons that yield precise gene knockouts. However, screening hundreds of clones for a single-nucleotide edit remains a challenge, especially in the absence of a phenotype. The Guide-it Knockin Screening Kit provides the ability to quickly identify edited clones in 96-well plates, employing a simple and rapid workflow that comprises PCR amplification of the genomic target site followed by an enzymatic assay with a fluorescent readout. Click on the links below to learn more.