Left boundary flanking sequence of exogenous event inserting vector for transgenic rape T45 and its application
A technology of exogenous insertion and flanking sequences, which can be used in applications, genetic engineering, plant genetic improvement, etc., and can solve problems such as specificity and characterization that have not yet been found
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[0041] 1. PCR amplification of sequences flanking the left border of the transgenic rapeseed T45 event exogenous insertion vector
[0042] First preheat 20% SDS to 65°C, take 15ml SDS extraction buffer (0.1TrisHCl, 0.05MEDTA, 1M NaCl pH8.0) and add it to a 50ml centrifuge tube, then add 2.5μl β-mercaptoethanol and mix well; liquid nitrogen Grind about 3g of leaves, transfer the powder to 50ml of a 50ml centrifuge tube containing extraction buffer, shake and mix on a shaker, add 2ml of preheated 20% SDS, mix well, and bathe in 65°C water for at least 30 minutes, during which time Shake the test tube gently; after the water bath, quickly place the centrifuge tube on ice, add 3ml 3M KAc, mix well, and place it on ice for 30 minutes; centrifuge at 5000g at 4°C for 5min; transfer the supernatant to a new 50ml centrifuge tube, Add 2 / 3 volume of isopropanol, mix well, place at -20°C for more than 30min; centrifuge at 6000g, 4°C for 15min, pour off the supernatant, wash with 75% ethan...
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