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. Author manuscript; available in PMC: 2014 Mar 5.
Published in final edited form as: Biochemistry. 2013 Feb 21;52(9):1547–1558. doi: 10.1021/bi301008r

Figure 1.

Figure 1

C18 RP-HPLC and ESI-MS analysis of purified recombinant pro-cathelicidin, LL-37 and hCLD. Proteins were analyzed on a Waters XBridge BEH130 C18 column (4.6 × 150 mm, 3.5μm) using a linear gradient of 5 – 65% acetonitrile at a flow rate of 1 mL/min over 30 min. The experimental values of the molecular masses of the desired products are shown together with expected values calculated based on the average isotope compositions (in parentheses).