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. 2012 Sep;53(9):1993–2001. doi: 10.1194/jlr.D028746

Fig. 1.

Fig. 1.

Fluorescence emission spectra of ADIFAB excited at 386 nm in (A) Hepes buffer without (○) and with 1 μM each of LOPC(■) and OA(△). B: Hepes buffer without (○) and with 1 μM each of LPPC(■) and PA(△). Acrylodan is displaced and its fluorescence emission shifts to the red region of the spectrum upon binding of LPC and FA to the ADIFAB protein.