A Molecular Marker Affecting the Loin Circumference Traits of Duroc Pigs and Its Application
A technology of molecular markers and traits, applied in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., can solve the economic loss of pig farming enterprises without systematic and detailed research on waistline phenotype selection and determination , the reduction in the utilization rate of breeding pigs and other issues, to achieve the effect of improving the body shape selection process, increasing sales profits, and improving core competitiveness
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Embodiment 1
[0032] (1) Experimental animals
[0033] The experimental pig group used in this example is 627 purebred American Durocs of Guangdong Wenshi Breeding Pig Technology Co., Ltd., which is the core group of the breeding pig branch company, and the group pedigree records are detailed.
[0034] In this experiment, Chinese and American Duroc pigs were selected from this resource group. The pigs have free access to food and water, and the entire feeding method and feeding conditions are always consistent, which is a conventional method.
[0035] Duroc pigs have a small number of litters, with an average of only 9 to 10 pigs in a large group, but they grow fast, have a high feed conversion rate, a high carcass lean meat rate, a high intramuscular fat content, and strong stress resistance. Domestic commercial pig production has established a relatively mature hybrid supporting system. Among them, Du Dachang's hybrid combination continues to maintain an absolute dominant position in my ...
Embodiment 2
[0049] Example 2 Target DNA sequence amplification and sequencing
[0050] (1) Primer design
[0051] The DNA sequence of SEQ ID NO.1 on pig chromosome 4 was downloaded from Ensembl website (http: / / asia.ensembl.org / index.html). And use primer design software primer premier 6.0 to design primers. The DNA sequences of the designed primers are as follows:
[0052] Primer C-F: 5'-GGGTGAGGGTGGGATTAG-3';
[0053] Primer C-R: 5'-TTGCGTTAGTGATTGTCCTG-3';
[0054] (2) PCR amplification
[0055] Add 1 μL of DNA template, 3.4 μL of double distilled water, 5 μL of 2×Tag PCR StanMixwithLoading Dye, and 0.3 μL of primers C-F and C-R into the 10 μL reaction system. The PCR reaction conditions were as follows: 5 minutes of pre-denaturation at 94°C, 35 cycles of denaturation at 94°C for 30 s, annealing at 54.3°C for 30 s, extension at 72°C for 45 s, and finally 5 min at 72°C.
[0056] (3) DNA sequence determination
[0057] Finally, the PCR-amplified products were sequenced, and the seq...
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