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Co-immunoprecipitation (Co-IP) assay Cells after indicated treatments were lysed in IP buffer (50 mM Tris-HCl, pH 7.5, 0.5% NP-40 (MF430, Mei5bio), 150 mM NaCl, 5 mM EDTA, 10% Glycerin) with protease inhibitor cocktail (B14001, Bimake) for 30 min at 4 C, followed by the enrichment of target proteins using Flag-M2 beads (B23102, Bimake) or specific antibodies overnight at 4 C

With one set of 20 strokes and another set of 10 strokes, the remaining sample was homogenized using a 2-ml homogenizer

Khaled Abd EA, Hanan N, Shwikar A, Ahmed E, Hany A, Doaa H

Additional research is exploring its influence on oxidative stress response, immune modulation, and cellular communication involved in tissue repair and remodeling

A multi-center, cross-sectional study on quality of life in cutaneous lupus erythematosus patients

Irreversible spectrin-haemoglobin crosslinking in vivo : a marker for red cell senescence