SNPs primers for detecting type 2 diabetes risk and application thereof
A type 2 diabetes and risk technology, applied in the field of SNPs primers, can solve the problem of low risk accuracy and achieve the effect of increasing body movement, high efficiency, and improving accuracy
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[0041] Sample collection and arrangement:
[0042] The inventor collected blood samples from 222 patients with type 2 diabetes and 140 normal controls from Ningbo Lihuili Hospital between May 2011 and April 2012 for research.
[0043] DNA was extracted using whole blood genomic DNA extraction kit (BioTeke, China), and the specific steps were as follows:
[0044] 1) Add 900 μL red blood cell lysate to a 1.5 mL microcentrifuge tube.
[0045] 2) Mix the anticoagulated blood thoroughly, and add 300 μL to the erythrocyte lysate in step 1.
[0046] 3) Let stand at room temperature for 10 minutes.
[0047] 4) Centrifuge at 12000 rpm for 20 seconds. Carefully remove the red supernatant and vortex for 15 seconds.
[0048] 5) Add 300 μL of nuclear lysate, and flick the centrifuge tube several times quickly and vigorously.
[0049] 6) Add 30 μg / mL RNase A, mix thoroughly, incubate at 37°C for 15 minutes, and then let stand to room temperature.
[0050] 7) Add 100 μL of protein prec...
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