Polypeptide with function of reducing uric acid and application of polypeptide
A technology for reducing uric acid and activity, applied in the field of peptides
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Embodiment 1
[0040] Take 100μl 18mg / ml Tyr-Glu-Gly solution in a 10ml centrifuge tube, add 50μl xanthine oxidase, incubate in a water bath at 30°C for 10min; add 2.9ml of the Tris-HCl buffer solution with pH 8.0, 400μl xanthine Standard stock solution, kept at 30°C for 20 minutes in a water bath; after the reaction, add 150 μl of 1M HCl, pass through a 0.22 μm aqueous membrane after cooling, replace the peptide sample with pH 8.0 Tris-HCl buffer as a blank control, and wait for the test.
Embodiment 2
[0042] Take 100μl 16mg / ml Tyr-Glu-Gly solution in a 10ml centrifuge tube, add 50μl xanthine oxidase, incubate in a water bath at 30°C for 10min; add 2.9ml of the Tris-HCl buffer solution with pH8. The stock solution was incubated in a water bath at 30°C for 20 minutes; after the reaction, 150 μl of 1M HCl was added, cooled and passed through a 0.22 μm aqueous membrane, and the peptide sample was replaced with pH 8.0 Tris-HCl buffer as a blank control, to be tested.
Embodiment 3
[0044] Take 100μl 14mg / ml Tyr-Glu-Gly solution in a 10ml centrifuge tube, add 50μl xanthine oxidase, incubate in a water bath at 30°C for 10min; add 2.9ml of the Tris-HCl buffer solution with pH8. The stock solution was incubated in a water bath at 30°C for 20 minutes; after the reaction, 150 μl of 1M HCl was added, cooled and passed through a 0.22 μm aqueous membrane, and the peptide sample was replaced with pH 8.0 Tris-HCl buffer as a blank control, to be tested.
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