Figure 1From: Altering the selection capabilities of common cloning vectors via restriction enzyme mediated gene disruptionStrategies employed for cloning a kanamycin resistance cassette ( kanR) via selectable marker restriction enzyme mediated gene disruption. The cassette was cloned into the unique Sca I site present in the ampR gene of pUC19 and pBlueScript SK+. Relevant restriction sites and features of each vector are indicated.Back to article page