The sample extracts were kept dry at room temperature for ~50 years. These were the sample extracts studied here. One concern when analyzing a HCS assay preserved sample set that is 50 years old is the possibility of contamination over time. We did not find any blanks that had been stored under identical conditions as the sample extracts upon discovery of the sample set. Therefore sample analysis results could not be compared to blank analytical results retrieved

from an identical analytical protocol to assess the level of blank contamination. However, procedural blanks were generated and subjected to the same sample preparation and analysis scheme as the samples themselves. Analysis of procedural blanks for targeted organic species revealed that contamination from sample preparation SN-38 nmr and analysis was negligible. Furthermore, the samples remained sealed and unopened until their analysis, to prevent contamination from water vapor and oxygen. However, the samples were not initially sealed Lazertinib cell line under anaerobic conditions so it is possible that there was some oxygen present in the sealed tubes, which may have oxidized some of the species present in the sample extracts over time. When Miller moved from Columbia University to the University of California, San Diego in 1960, he took

the vials described above with him, together with the products of many other experiments he had conducted earlier while at the University of Chicago (Johnson et al. 2008). These were stored in a cardboard box until we

Amine dehydrogenase rediscovered them a few months before his death on May 20, 2007. Chemicals and Reagents All glassware and sample handling tools were rinsed with Millipore water (18.2 MΩ, <10 ppb total organic carbon), wrapped in aluminum foil, and then heated in air at 500 ºC overnight. All of the chemicals used in this study were purchased from Sigma-Aldrich or Fisher Scientific. Stock amino acid solutions (~10−3 M) were prepared by mixing individual amino acid crystals (97–99% purity) with doubly distilled (dd) H2O. The reagent o-phthaldialdehyde/N-acetyl-L-cysteine (OPA/NAC) was used as a chemical tag for the fluorescence detection and enantiomeric separation of primary amines. The derivatization solution was prepared by dissolving 4 mg OPA in 300 μL methanol (Fisher Optima), and then adding 250 μL 0.4 M sodium borate buffer (pH 9.4), 435 μL H2O, and 15 μL of 1 M NAC. The ammonium formate buffer used in the time of flight-mass spectrometry (ToF-MS) analyses described below was prepared by NH4OH titration of a 50 mM formic acid solution to pH 8. A 1 μM phenolphthalein solution in acetonitrile with 0.1% formic acid was used for mass calibration of the ToF-MS via an independent electrospray emitter (Glavin and Dworkin 2009).