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. 2007 Aug 7;35(15):e100. doi: 10.1093/nar/gkm575

Figure 2.

Figure 2.

ESI–FT ICR MS analysis of reaction products. The substrate dsDNA was reacted with 0 (A), 100 (B) or 200 (C) nM CTD. The products were purified according to the protocol described in MATERIALS AND METHODS section. The deconvoluted spectra of reacted products of 5′-phosphorylated 17-bp dsDNA were shown. For clarity, information concerning the length and measured mass of the major species are shown above the corresponding peaks.