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My protocol: lysate in RIPA buffer; 1D in pre-cast 4-12% gradient gel; transfer at 30V over 2 h; block in 8% non-fat milk in tris-buffered saline with 0.1% tween 20 (TBS-T); incubate with primary...
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I've transferred HepG2 cells from DMEM/F12 to DMEM with high glucose. They look fine in the first 24 hr, then they inevitably start clumping . Any suggestions on how to avoid this?
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