A kind of preparation method of cold shock protein
A technology for cold shock protein and protein solution, applied in the field of preparation, can solve problems such as no biological activity, and achieve the effects of simplified preparation conditions and large yield
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[0018] The preferred embodiments of the present invention are given below in conjunction with the accompanying drawings to describe the technical solution of the present invention in detail.
[0019] The preparation method of the cold shock protein of the present invention comprises the following steps:
[0020] Step 1: Extract total RNA by TRIzol method; grind mouse tissue samples with a mortar, add 1ml of lysate for every 50-100mg of tissue, rinse cells with PBS, add 1ml of TRIzol reagent, blow and mix, transfer to 1.5ml EP tube, Then add chloroform for extraction, fully wash the precipitate with 75% ethanol, remove the supernatant after centrifugation, dissolve with DEPC water after drying, and store at -70°C for future use.
[0021] Step 2, eDNA first-strand synthesis Add 5 μl RNA solution, 1 μl Oligo(dT), 1 μl dNTP to 20 μl reaction system, react at 65°C for 5 minutes, and quickly cool on ice. Then add 4 μl buffer (buffer), 2 μl DTT (dithiothreitol), 1 μl Rnase inhibitor...
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