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doi: 10.1093/humupd/dmab026 166

The catalytic degradation of UA was monitored by recording the changes in absorbance at 290 nm every 10 min using a UVVis spectrophotometer

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After blocking with blocking solution (0.2% casein, 0.3% Triton X-100, and 3% goat serum diluted in PBS) for 2 h at room temperature, anti-C3 (1:100 dilution) antibody-stained sections were reacted overnight at 4 C

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