Method and special primer set for identifying facticity to-be-tested variety belonging to CCRI 63
A primer pair and auxiliary identification technology, applied in biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., can solve problems such as counterfeiting, affecting the promotion effect of hybrid cotton, and affecting seed sales
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Embodiment 1
[0029] Example 1. Construction of the DNA fingerprint of China Cotton Institute 63
[0030] 1. Screening of SSR primer pairs
[0031] After a large number of cotton SSR primer screenings, it was found that 30 SSR primer pairs (nucleotide sequences are shown in Table 1) can be used to make the DNA fingerprint of China Cotton Institute 63.
[0032] Table 130 nucleotide sequences of primer pairs
[0033] Serial number
Primer name
Forward primer (5’→3’)
Reverse primer (5’→3’)
1
CIR62
TTTAGAGGAGAAGTTTAGG (sequence 1)
CAGTCTCTTGTAGTTTCATT (sequence 2)
2
CS62
GATGGCTACCTCCCTTTGTA (sequence 3)
CGTAAGGAAGCCTAGCAAAA (sequence 4)
3
NAU1070
ACCAACAATGGTGACCTCTT (sequence 5)
CCCTCCATAACCAAAAGTTG (Sequence 6)
4
NAU1102
ATCTCTCTGTCTCCCCCTTC (serial 7)
GCATATCTGGCGGGTATAAT (Sequence 8)
5
NAU1186
AATGGTCCTGCTCCAGATT (sequence 9)
AATCGTCGTCGTCGAATTAT (sequence 10)
6
NAU2026
GAATCTCGAAAACCCCATCT (sequence 11)
ATTTGGAAGCGAAGTACCAG (sequence 12)
7
NAU2173
GCCAAATAGGTCACACA...
Embodiment 2
[0073] Example 2. Application of 30 SSR primer pairs to assist in the identification of China Cotton Institute 63
[0074] The following cotton varieties were tested: Zhongzhimian No. 2 (Institute of Plant Protection, Chinese Academy of Agricultural Sciences), Ruiza 816 (Jinan Xinrui Seed Industry), Handan 8266 (Handan Academy of Agricultural Sciences), China Cotton Institute 63 ( China Cotton Seed Industry).
[0075] Detection method: extracting genomic DNA of cotton leaves, using genomic DNA as a template, respectively using the 30 SSR primer pairs for PCR amplification, and then performing 8% polyacrylamide gel electrophoresis and silver staining for color development.
[0076] The PCR system and PCR reaction procedures are the same as in Example 1.
[0077] See electrophoresis Figure 31 (1, 2, 3, 4 represent Zhongmian Institute 63, Zhongzhimian 2, Ruiza 816 and Han 8266, respectively). See Table 3 for the banding results.
[0078] Table 3 Band patterns after amplification of geno...
Embodiment 3
[0113] Example 3. Using 20 primer pairs among 30 SSR primer pairs to identify seed purity
[0114] A batch of China Cotton Institute 63 is collected from the seed production company (in the form of seeds, a total of 200 seeds; the seeds are theoretically China Cotton Institute 63, but usually due to the limited operation level in the seed production process, it is difficult to achieve 100% purity. Female parent plant phenomenon or other adulteration phenomenon), randomly select 26 seeds from 200 seeds, extract the genomic DNA of the seeds, use the genomic DNA as the template, and use 20 SSR primer pairs (see the table for specific SSR primer pairs) 4) Perform PCR amplification, and then perform 8% polyacrylamide gel electrophoresis and silver staining for color development. Using the genomic DNA of the male parent of China Cotton Institute 63 (2 replicate samples) as a template, respectively, 20 SSR primer pairs were used for PCR amplification, and then 8% polyacrylamide gel elec...
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