A microfluidic chip-based method for typing serum glucose profiles
A microfluidic chip and typing method technology, applied in the field of sugar analysis, can solve problems such as long-term separation mode, and achieve the effects of rapid separation and analysis capability, efficient separation and detection, and high resolution
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[0018] 1) Selection of electrophoresis buffer system:
[0019] The injection buffer system consists of 50mmol / L tris(Tris), 50mmol / L N-tris(hydroxymethyl)methyl-3-aminopropanesulfonic acid (TAPS), 1mmmol / L ethylenediaminetetra Acetic acid (EDTA) is composed of 1×TTE buffer solution, pH8.3; the sample separation system is composed of POP 4 or POP 7 gel;
[0020] 2) Preparation and labeling of serum samples
[0021] Take 100μL of blood, centrifuge at 3000r / min for 10min to separate the serum, add 2μL of 10mmol / lNH to the 2μL serum sample 4 HCO 3 Buffer and 3 μL deionized water, heat at 95°C for 5 minutes, put in the refrigerator (4°C) for about 15 minutes, add N-glycopeptidase F, incubate in a 37°C incubator for 12 hours (or overnight), and put it in the refrigerator (4°C) ) in an ice bath for 15 minutes, centrifuged for 15 minutes, and the supernatant after centrifugation was used for determination; take 6 μL of centrifuged and dried at 60°C for 120 minutes without a cover (...
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