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Cleavage Phase (During Processing) Buffer exchange first: Move from elution buffer to cleavage buffer Never assume elution conditions are compatible Start with pilot experiments: Small scale (100 g) Time course (1h, 2h, 4h, 16h) Multiple protease ratios (1:50, 1:100, 1:200) Monitor by SDS-PAGE: Look for: Band shift, new bands, loss of material Quantify cleavage efficiency Scale up conservatively: Optimal conditions at small scale may not translate directly Verify at each scale Post-Cleavage Phase (Cleanup) Remove uncleaved protein: Subtractive affinity (if cleaved protein doesn't bind) Ion exchange (if charge difference sufficient) Size exclusion (if size difference sufficient) Remove protease: Use orthogonally-tagged protease Or: Accept co-purification if protease doesn't interfere Verify final product: SDS-PAGE: Single band

Mol Cell Neurosci 120:103722 Koak , Sarac S, Aydogan E, entrk E, Akakn D, Koroglu K, zer F (2017) Evaluation of the possible protective role of naringenin on gentamicin-induced ototoxicity: a preliminary study

After that, the wells were loaded with 5 M of DCFH-DA and incubated for 30 min at 37 C

Glaucoma: from pathogenic mechanisms to retinal glial cell response to damage

HHcy may contribute to the overactivation of Th1 and Th17 cells in the pathogenesis of psoriasis