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. 2006 Aug 7;34(13):3722–3730. doi: 10.1093/nar/gkl503

Figure 1.

Figure 1

Plasmid with BsmAI restriction site and fragment lengths relevant to the detection of mutation. An oligonucleotide with damaged sites was inserted at the SmaI restriction site of pUC18. Misrepair of the damage leads to ‘mutant’ fragment of 1755 bp length, whereas successful repair results in 1352 and 403 bp fragments after digestion with BsmAI.