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For uricase intervention experiments during PM 10 and OVA co-exposure, groups of mice were exposed to intranasal saline, OVA (100 g)/PM 10 (200 g), or OVA (100 g)/PM 10 (200 g)/uricase (10 U) in fixed volumes of 50 l phosphate-buffered saline on days 1, 3, and 5

The methods employed and their corresponding examples are discussed in detail below ( Figure 1

Its molecular structure has made it a subject of interest in laboratory environments where peptide stability and consistency are required

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