Tetrachloroauric acid

Tetrachloroauric acid (0.01-10 mM) induces concentration-dependent structural perturbations in DMPC multibilayers, disrupting bilayer structure at 0.1-3 mM and promoting reordering at 5-10 mM^[1].
Tetrachloroauric acid (0.01-10 mM) induces mild, concentration-dependent structural perturbation in DMPE multibilayers, with less disruption than observed in DMPC multibilayers^[1].
Tetrachloroauric acid (0.01-0.1 mM; 18 °C, 37 °C) increases lipid packing order at the polar headgroup and acyl chain regions of DMPC LUVs at 18 °C and 37 °C, with a more pronounced effect at 37 °C^[1].
Tetrachloroauric acid (0.01-0.1 mM; 37 °C) induces non-monotonic changes in lipid packing order in isolated unsealed human erythrocyte membranes at 37 °C, with distinct minima and maxima at specific concentrations^[1].
Tetrachloroauric acid (0.01-0.1 mM; 18 °C, 37 °C) reduces DPH fluorescence lifetime (indicating increased interchain hydration) and increases rotational correlation time (indicating reduced rotational diffusion) in DMPC LUVs at 18 °C and 37 °C, with concentration-dependent response kinetics^[1].
Tetrachloroauric acid (0.01-0.07 mM; 37 °C) induces minor, non-monotonic changes in DPH fluorescence lifetime and rotational correlation time in isolated unsealed human erythrocyte membranes at 37 °C, indicating milder effects than in DMPC LUVs^[1].
Tetrachloroauric acid (0.1-10 mM) induces concentration-dependent morphological changes in intact human erythrocytes, transitioning from stomatocytes/spherostomatocytes at low concentrations to elliptocytes/knizocytes at high concentrations^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.