SNP (single nucleotide polymorphism) marker for Chinese cabbage type crop bolting and flowering identification
A crop and marker technology, applied in the direction of recombinant DNA technology, DNA/RNA fragments, etc., can solve the problem that the BrFLC5 gene cannot be transcribed normally
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[0071] Example 1: Identification of Pi3+1(G-A) variation in BrFLC5 in Chinese cabbage varieties using SNP markers developed based on KASP technology.
[0072] (1) Extraction of whole-genome DNA of Chinese cabbage varieties: take the leaf tissues of Chinese cabbage varieties to be tested (281 parts of Chinese cabbage), extract whole-genome DNA by CTAB method, and dilute the whole-genome DNA of each Chinese cabbage variety to 15 ng / μl;
[0073] (2) Dilute primers: Dilute according to the primer dilution information provided by the synthetic primer company. First, centrifuge the dry powder primers to prevent splashing of the dry powder primers near the nozzle when opening the cap. According to the primer dilution information, dilute the forward FAM fluorescent primers, The concentration of forward VIC fluorescent primer and reverse primer (sequence information as shown in SEQ ID NO: 1, SEQ ID NO: 2 and SEQ ID NO: 3 in the sequence table) was diluted to 10 μM;
[0074] (3) Prepare...
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