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The fluorescence analyses were performed using a BX41 Olympus upright microscope.
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Quantitative fluorescence analyses were performed using ImageJ software.
Flow cytometry acquisitions and analyses were performed using a three-laser Becton Dickinson fluorescence-activated cell sorter (FACSAria).
Aflatoxin B1 (AF B1) analyses were performed using a HPLC instrument consisting of two chromatographic pumps, sampling system, and fluorescence detector (HPLC-FLD).
Real-time PCR quantitative mRNA analyses were performed using SYBR green fluorescence (Stratagene, Cedar Creek, TX).
Gene-level analyses were performed using the mean normalized fluorescence values for all probes and replicates.
Water arsenic analyses were performed using continuous flow hydride generation atomic fluorescence spectroscopy (HGAFS).
In vitro analyses were performed using MCF7 breast cancer cells, which included immunoprecipitations and Fluorescence Resonance Energy Transfer FRETT) analyses to illustrate ERα complex formation.
The emitted fluorescence of EGFP was measured in log scale at 530 nm (FITC band pass filter) and the analyses were performed using CellQuestPro software (Becton Dickinson).
Statistical analyses were performed using STAMP26.
Statistical analyses were performed using GraphPad Prism.
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