A method for detecting short-chain fatty acids in serum and lymphoid tissue based on gc-ms
A technology for medium and short-chain fatty acids and lymphoid tissue, applied in the field of analytical chemistry, can solve the problems of complicated operation steps, low recovery rate results, high time cost, and achieve the effects of good repeatability and high recovery rate.
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Embodiment 1
[0040] (1) Instruments and reagents
[0041] Agilent 7890A gas chromatograph (Agilent Technology, USA); IKA VORTEX 3 vortex mixer (IKA, Germany); HH-S constant temperature water bath (Jintan Medical Instrument Factory, China); Refrigerated centrifuge (Thermo Fisher, USA) ); Milli-Q ultrapure water system (Millipore, USA).
[0042] Acetic acid, propionic acid, butyric acid, 2-ethylbutyric acid, pentafluorobromoben (Sigma-Aldrich, USA); Acetone, n-hexane (China Comeo Reagent Co., Ltd.); Phosphate buffer (China Dingguo Biological Reagent) company);
[0043] (2) Sample pretreatment
[0044] Serum: Leave the collected whole blood at room temperature for 30 minutes, centrifuge for 20 minutes at 4°C and 2000 rpm, and take the supernatant;
[0045] Lymphoid tissue: Accurately weigh 50mg of lymphoid tissue, add 1mL of pre-cooled ultrapure water, use a tissue grinder to grind evenly at 4°C, vortex vigorously for 1min, extract by ultrasonic for 15min, centrifuge at 4°C 10000rpm for 10...
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