N-Acetyl L-Tyrosine
This page depicts the oxidation of N-Acetyl L-Tyrosine (NAT) by Horse Radish Peroxidase (HRP). Each sample of NAT was dissolved in pH 5 phosphate citrate buffer. The method used on the HPLC was "HPA_0604156".
The Dioxane Conundrum
The following two graphs depict the difference in reaction when dioxane is present and when it is not. The conclusion is that dioxane quenches the oxidation of NAT.
Beaker Reaction vs. Immobilized Enzyme Bio-Reactor
The following graphs depict the difference in HPLC data when the reaction is conducted in a beaker and when the reaction is ran using the immobilized enzyme technique using a bio-reactor.
Concentration Test
These graphs depict the difference in concentration of NAT and H2O2. Increasing the concentration will help to obtain more products.
Flash Chromatography
The objective of flash chromatography is to isolate peaks seen in the HPLC. Running flash chromatography allows for the product to be isolated.
The following graphs show the difference between running the flash system under conditions with wavelength at 276 and 300 with 223 and 276. The first graph is the NAT standard ran through the HPLC. The two flash chromatography graphs show the difference in changing the methods of the flash system.
The following graph shows a difference between
Antioxidants in Reaction
The following graph depicts the oxidation of 2mM NAT by H2O2 with various concentrations of ascorbic acid in pH 5 buffer.
The following is the oxidation of 2mM NAT by H2O2 with various concentrations of reduced GSH in pH 5 buffer.