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. Author manuscript; available in PMC: 2011 Nov 11.
Published in final edited form as: Chem Commun (Camb). 2011 Oct 5;47(43):11936–11938. doi: 10.1039/c1cc15124j

Fig. 2.

Fig. 2

Representative chromatograms of trimethylsilylated derivatized hydroxylated products (ω1, ω2, ω3) from reactions of 3 μM BM3 enzymes with 1.5 mM lauric acid for 2 h. 12-Hydroxydodecanoic acid was used as internal standard (I.S., 10 nmol).