Promoter miR172c and application thereof
A fragment and sequence technology, which is applied to the promoter miR172c and its application fields, can solve the problems of gene expression accumulation in the outer edge, affecting the growth and development of plants, etc., and achieve the effect of strong specific expression activity.
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[0024] Example 1. Preparation of promoter and verification of specific expression
[0025] 1. Preparation and confirmation of the promoter
[0026] 1. Extraction of rice genomic DNA
[0027] (1) Take the leaves of Nipponbare rice, add liquid nitrogen, after fully grinding, pour the powder into a 1.5ml centrifuge tube;
[0028] (2) After the liquid nitrogen in the centrifuge tube is completely volatilized, immediately add 500ul DNA extraction buffer (0.1mol / LTris HCl (pH 8.0), 0.5mol / L NaCl, 0.05mol / L EDTA, 0.5% SDS), fully After mixing, incubate at 65°C for 30 minutes, during which the centrifuge tube is gently inverted up and down to fully mix the sample with the buffer;
[0029] (3) Centrifuge at room temperature for 15 minutes at 12,000 rpm;
[0030] (4) Transfer the supernatant to another centrifuge tube;
[0031] (5) Add an equal volume of tris-phenol and extract once;
[0032] (6) Extract again with equal volume of chloroform;
[0033] (7) Take the supernatant, add...
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