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2 protocols using l methionine

1

Amino Acid and Compound Acquisition Protocol

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L-Alanine (CAS No. 56-41-7), L-Arginine (CAS No. 74-79-3), L-Asparagine (CAS No. 70-47-3), L-Aspartic acid (CAS No. 56-84-8), L-Cysteine (CAS No. 52-90-4), L-Glutamic acid (CAS No. 56-86-0), L-Glutamine (CAS No. 56-85-9), L-Histidine (CAS No. 71-00-1), L-Isoleucine (CAS No. 73-32-5), L-Leucine (CAS No. 61-90-5), L-Lysine (CAS No. 56-87-1), L-Methionine (CAS No. 63-68-3), L-Phenylalanine (CAS No. 63-91-2), L-Proline (CAS No. 147-87-3), L-Serine (CAS No. 56-45-1), L-Threonine (CAS No. 72-19-5), L-Tryptophan (CAS No. 73-22-3), L-Tyrosine (CAS No. 60-18-4), L-Valine (CAS No. 72-18-4), and Glycine (CAS No. 56-40-6) were purchased from MACKLIN. MHY1485 (CAS No. 326914-06-1) and Rapamycin (CAS No. 53123-88-9) were purchased from APExBIO.
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2

Evaluation of Cu NZs@PLGA Nanofibers' O2·- Scavenging Activity

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The O2· depletion activity of Cu NZs@PLGA nanofibers was investigated via the nitroblue tetrazolium (NBT) chromogenic method. Cu NZs@PLGA nanofibers were immersed in Tris-HCl buffer (10 mM, pH 7.4) (Biosharp, China) with a final Cu NZs concentration of 150 ng mL−1. After 0, 2, 6, or 12 h preincubation, the working solution containing 6.5 mM l-methionine (C11385354, Macklin, China), 37.5 μM NBT (C11167116, Macklin, China), and 10 μM riboflavin (C11507808, Macklin, China) was homogeneously mixed with the pre-treated Tris-HCl solutions, respectively, and irradiated using a SCIENTZ03-II UV radiation instrument (Scientz, China) with a wavelength of 254 nm (60 W, 150 mm) for 3 min at RT. UV irradiation resulted in the generation of O2· from riboflavin and l-methionine, which further converted NBT to blue formazan. After illumination, the absorbances of the mixtures were measured by a UV–Vis spectrophotometer at a wavelength of 560 nm. The clearance rate of O2· was calculated according to the same formula of H2O2 clearance rate.
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