Preparation of a trace, efficient and stable triglyceride detection kit in adipocytes
A fat cell and triglyceride technology, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, etc., can solve the problems of high absorbance, easily damaged cell layer, oily red residue, etc., and achieves simple operation steps and reduces experiments. Time, high throughput effect
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[0027] Preadipocytes were isolated and purified from the subcutaneous adipose tissue of the neck and back of Tibetan pigs 2 days after birth, and differentiated by cocktail method (Insulin, Dex, IBMX) + rosiglitazone, and the cells on day 12 after differentiation were used for the experiment. No. 5 formula of the present invention is used in the experiment, and the detailed steps are as follows:
[0028] Step 1: Induce the differentiation of Tibetan pig preadipocytes in a 96-well plate for 12 days, take out the plate from the incubator, carefully suck off the culture medium, and pay attention not to touch the underlying cells with the tip of the pipette;
[0029] Step 2: Wash twice with PBS (200 ul / well), as gently as possible. After washing, add 200 ul of PBS to each well;
[0030] Step 3: Add 5 ul of Nile Red working solution and incubate at room temperature (20-25°C) in the dark for 5 minutes;
[0031] Step 4: Place the orifice plate in a microplate reader, and set a wavel...
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