Intracellular amino acid metabolic profiling analysis method
A metabolic profile and analysis method technology, applied in the field of high-throughput analysis of intracellular amino acid metabolic profile, can solve problems such as difficulty in obtaining metabolome data, achieve high throughput of cell culture and operation, avoid the influence of intracellular metabolism, and optimize Effect of extracting repeatability and recovery
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Embodiment 1
[0026] Investigation on the analysis method of intracellular amino acid metabolism profiling in a small number of cells:
[0027] 1) Inoculate and culture HepG2 cells on a 96-well plate
[0028] at 175cm 2 HepG2 cells were adherently cultured in cell culture flasks: DMEM high-glucose medium with 10% FBS was given, and the cells were grown to 60-70% confluence at 37°C and 5% CO2 under constant conditions.
[0029] Cells were trypsinized and resuspended in DMEM medium containing 10% FBS. For cell counting, prepare a density of 2 x 10 4 cells / ml of cell suspension was used to inoculate 96-well plates.
[0030]In a 96-well plate, 100 μL of the above-mentioned HepG2 cell suspension (the suspension was prepared with 10% FBS in DMEM medium) was inoculated in each well, and kept at 37° C. and 5% CO 2 for 48 hours.
[0031] 2) Cell quenching and intracellular metabolite extraction
[0032] After HepG2 cells grew for 48 hours, the cells growing in each well of the 96-well plate wer...
Embodiment 2
[0059] Profile analysis of intracellular amino acid metabolism in HepG2 cells with fatty acid intervention:
[0060] 1) HepG2 cell culture and fatty acid intervention
[0061] at 175cm 2 Adhesive culture of HepG2 cells in cell culture flasks: give 10% FBS in DMEM high-glucose medium, and grow the cells to 60-70% confluence at 37°C and 5% CO2 under constant conditions.
[0062] Cells were trypsinized and resuspended in DMEM with 10% FBS. For cell counting, prepare a density of 2 x 10 4 cells / ml of cell suspension was used to inoculate 96-well plates.
[0063]In a 96-well plate, 100 μL of the above-mentioned HepG2 cell suspension (the suspension was prepared with 10% FBS in DMEM medium) was inoculated in each well, and kept at 37° C. and 5% CO 2 for 24 hours.
[0064] After the cells grew for 24 hours, they were subjected to fatty acid intervention. The fatty acids applied were palmitic acid (PA, C16:0), palmitoleic acid (POA, C16:1) and combinations of both. The method of...
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