Method for detecting surface enhanced Raman spectra of blood RNA
A surface-enhanced Raman and spectral detection technology, applied in the application field of biomedical optical technology in life sciences, can solve the research reports of SERS spectral detection and other issues
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[0029] 1. Separate the serum from the whole blood of patients with colon cancer and normal people, and store it in a -80°C refrigerator within two hours to prevent RNA cleavage. Use Trizol LS reagent to extract RNA from serum, and use 30 μL DEPC water Dissolve the RNA and store it in a -80°C refrigerator for later use. Use NanoDrop ND 1000 to quantify the RNA at a concentration of 18.8 to 56.4 ng / mL.
[0030]2. Dissolve 10 mg of silver nitrate in 50 ml of deionized water, heat to 100°C to make it boil, then add 1 ml of trisodium citrate with a concentration of 1% dropwise, and stir rapidly, after the dropwise addition Continue to keep boiling for 6 hours to obtain silver sol. After the silver sol is naturally cooled, use a centrifuge to centrifuge the above silver sol at 10,000 rpm for 10 minutes to make the silver sol layered. The supernatant is discarded, and the concentrated silver sol in the lower layer is taken.
[0031] 3. Take 5 μl of concentrated silver sol and drop it...
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