Method for authenticating Beijing fatty chickens by microsatellite markers
A technology of microsatellite marking and fried chicken, which is applied in the application field of microsatellite marking, can solve the problems of restricting the preservation and development of chicken breeds, and achieve the effect of low detection cost, high accuracy and easy operation
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Embodiment 1
[0011] Example 1 Obtaining of SSR markers of the present invention
[0012] 100 original breeds of Beijing oil chicken and 40 original breeds of 5 reference breeds (Jingxing yellow chicken D2 line, silky silky chicken, Shiqi mixed chicken, Xianju chicken, Camellia chicken) were randomly selected. The Beijing oil chicken breed comes from the National Breed Preservation Farm of Beijing Institute of Animal Husbandry and Veterinary Medicine, Chinese Academy of Agricultural Sciences. The ratio of male to female is 1:1. Finally, the genomic DNA of 93 Beijing oil chickens and 40 chickens of other chicken breeds were obtained. 20 pairs of chicken-specific microsatellite markers were used for detection, and the polymorphisms of 19 microsatellite loci could not distinguish Beijing Youji chicken from other populations, and only the length polymorphism of LEI0070 marker in Beijing Youji chicken population had Characteristic, which can distinguish the Beijing Youjibao population from oth...
Embodiment 2
[0015] Embodiment 2 Utilizes the method of SSR marker to identify Beijing fried chicken
[0016] 1.1 Groups to be identified
[0017] Randomly select 40-50 chickens to be tested, the ratio of male to female is 1:1, blood is collected from the wing vein, anticoagulated with ACD, and stored at -20°C for later use.
[0018] 1.2 DNA extraction
[0019] The genomic DNA was extracted by the conventional phenol imitation method, dissolved in TE, and the purity and concentration of the DNA were double-checked by agarose gel electrophoresis and ultraviolet spectrophotometry, and then diluted to a concentration of 50ng / μl.
[0020] 1.3 Primers
[0021] According to chicken-specific SSR primers published in NCBI (http: / / www.ncbi.nlm.nih.gov / genome / sts / sts.cgi?uid=279930) (Table 2):
[0022] Table 2 SSR primers involved in the present invention
[0023]
[0024] 1.4 PCR reaction
[0025] PCR amplification was performed in a BioThermocycler. The PCR reaction program was pre-denatu...
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