• CloneCatcher™ Gold with a guaranteed minimum efficiency between 8 x 1010 and 1.2 x 1011* • Construct libraries of greater complexity than ever before • Library construction possible with small amounts of input DNA • Use less topoisomerase-loaded vector and reduce overall cost • Convenient single-use-tubes • Super-fast 10 minute protocol
Transferring exogenous DNA into E. coli is a standard laboratory method for cloning genes and constructing cDNA, genomic and epitope libraries. The limiting factor in many library-screening efforts or multiple fragment ligations is the efficiency by which DNA can be introduced into E. coli. Electroporation is one method to efficiently introduce DNA into E. coli.
CloneCatcher™ Gold are based on a proprietary method that allows rapid development and testing of new strains that are task specific. The resulting mutants have optimized performance profiles that produced substantially enhanced results.
Sharing your experience will help scientists like you. Achieve Reviewer Status and Win an iPad 3 (All reviews published will be entered into the next drawing on May 31st 2013).
