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Read Now: January Academic Times

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4 Short-term photo-illumination has negligible interference toward cell viability and functions of LDs

After the structural region comes a small integral membrane protein, p7, which seems to function as an ion channel 18,19

Previous assays have reported the use of low salt potassium phosphate buffers either as a component of the lipid substrates or as a diluent for the LPL source (e.g., PHP) to measure LPL activity where the NaCl concentration ranges from 0.1 to 0.3 M NaCl (Figure 3A), and therefore we recommend using 0.175 M NaCl when measuring LPL activity