LGR4 gene detection kit
A gene detection and kit technology, applied in the field of LGR4 gene detection kits, to achieve high sensitivity
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Embodiment 1
[0021] 1. Tissue total RNA extraction
[0022] (1) Tissue homogenate: Take about 20-30mg of each liver and add 1mL TRIZOL reagent to lyse. Homogenize with a homogenizer in an ice bath, transfer the sample to a 1.5mL centrifuge tube, and place at room temperature for 5min.
[0023] (2) Liquid phase separation: Operate in a special fume hood for RNA extraction, add chloroform at a ratio of 0.2mL / mL Trizol, shake vigorously and mix well, place at room temperature for 2-3min, and then centrifuge at 12000g for 15min at 4°C.
[0024] (3) RNA precipitation: Carefully transfer the upper aqueous phase to a new 1.5mL centrifuge tube, add isopropanol at a ratio of 1:1, leave it at room temperature for 10min, then centrifuge at 12000g, 4°C for 15min.
[0025] (4) RNA rinsing: After centrifugation, a white precipitate appeared at the bottom of the tube, remove the supernatant, rinse the RNA precipitate with 75% ethanol (made in DEPC water), centrifuge at 7500g, 4°C for 5min.
[0026] (5)...
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