A combination of molecular markers for germplasm identification of Litopenaeus vannamei and its application
A technology of molecular markers and Vannabin, which is applied in the field of aquatic animal genetics and breeding, can solve the problems of distinguishing different species, large differences, and difficulty in ensuring the authenticity of species and seedlings, and achieve the effect of improving accuracy
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Embodiment 1
[0027] Example 1: Development of a method for identification of Litopenaeus vannamei germplasm by combination of microsatellite markers
[0028] 1. Source of materials: Collection of germplasm materials from Zhengda, Kona Bay, SIS, Molokai, Ecuador, Kehai No. 1, and Guihai No. 1. Bay includes materials from 2012, 2014 and 2015, SIS includes materials from 2015 and 2016, materials from Guihai 1, Kehai 1, Molokai and Ecuador from 2014, the total number of samples 192.
[0029] 2. DNA extraction: The DNA of the above-mentioned materials was extracted using the Tiangen Plant Genome Extraction Kit. For the method, refer to the kit instructions. The concentration of the extracted DNA was measured using a Nanodrop 1000 (Thermo, USA), and stored in a -20°C refrigerator.
[0030] 3. Dilute the DNA extracted above to 50-100ng / μl respectively, use 13 pairs of high polymorphic microsatellite marker primers of the present invention to carry out PCR amplification, and the microsatellite pr...
Embodiment 2
[0038] Example 2: Application of the method for molecular identification of Litopenaeus vannamei germplasm
[0039] In view of the fact that the method established in the present invention has a high identification accuracy rate for different germplasms, the method of the present invention can be used to realize the identification of different germplasms of Litopenaeus vannamei and the species traceability of unknown source materials. The options offered are as follows:
[0040] 1. Collect germplasm materials from different domestic and international commercial germplasm companies. The number of individuals of each germplasm source is more than 30, and try to include materials from multiple generations and multiple regions. The DNA of the above-mentioned materials was extracted using the Tiangen Plant Genome Extraction Kit. For the method, refer to the kit instruction manual. The concentration of the extracted DNA was measured using a Nanodrop 1000 (Thermo, USA), and stored in...
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