1  as measured by fluorescence polarization of diphenylhexatriene.

2 8% increase in fluorescence anisotropy using diphenylhexatriene.

3  and anionic lipid probes, trimethylammonium diphenylhexatriene and cis-parinaric acid, embedded in e

4 the partition constant for trimethylammonium diphenylhexatriene and oleic acid, an average 2-fold inc

5 n packing with enhanced rotational motion of diphenylhexatriene (DPH) about its long axis were demons

6 fetime and rotational dynamics parameters of diphenylhexatriene (DPH) chain-labeled phosphatidylcholi

7 nd operationally simple method to synthesize diphenylhexatriene (DPH) is reported.

8 The average membrane location of a series of diphenylhexatriene (DPH)-derived membrane probes was ana

9 ophan excited-state energy to membrane-bound diphenylhexatriene (DPH).

10 ng order was determined from measurements of diphenylhexatriene fluorescence anisotropy decay.

11       DAG also caused an overall decrease in diphenylhexatriene fluorescence polarization (decreased

12  both stopped-flow fluorescence quenching of diphenylhexatriene in lipid bilayers and photoincorporat

13  sterols on the fluorescence polarization of diphenylhexatriene incorporated into DPPC-containing ves

14      Oxidation-induced fluorescence decay of diphenylhexatriene-labeled phosphatidylcholine (PC), equ

15 ydroergosterol), altering membrane fluidity (diphenylhexatriene) or membrane permeability (leakage as

16 fluorescent membrane probe trimethylammonium diphenylhexatriene (TMA-DPH).