SNP molecular markers related to sheep tail types and applications thereof
A technology of molecular markers and sheep, applied in the field of genetic biology, can solve the problems of lack of SNP molecular markers and achieve the effect of maintaining stability
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Embodiment 1
[0035] Example 1 Using the SNP molecular marker Chr13-49051930 to identify sheep tail type.
[0036] The test subjects were small-tailed Han sheep and Dorper sheep hybrid sheep (100), Ujumqin and Australian Merino hybrid sheep (100), Luxi black-headed sheep (100), small-tailed Han sheep (100), Tan sheep (50), Ujimqin sheep (50), Hu sheep (50), Sunit sheep (50), Cele black sheep (50), Bayinbulak sheep (50 ), one month old.
[0037] The specific primers for SNP molecular markers are:
[0038] Forward primer: 5'-TACGACCCTTTCATTGGGGG-3'
[0039] Reverse primer: 5'-ACAGTCACAGGTGGTGCAAT-3'
[0040] (1) Collect 5 mL of anterior vena cava blood from sheep, and extract DNA by phenol-chloroform method;
[0041] (2) Using the genomic DNA of the sheep to be tested as a template, PCR amplification was carried out using specific primers for SNP molecular markers. The amplification system was shown in Table 1, and the amplification procedure was shown in Table 2 to obtain PCR products; ...
Embodiment 2
[0049] Example 2 Using the SNP molecular marker Chr13-49132297 to identify sheep tail type.
[0050] The test subjects were small-tailed Han sheep and Dorper sheep hybrid sheep (100), Ujumqin and Australian Merino hybrid sheep (100), Luxi black-headed sheep (100), small-tailed Han sheep (100), Tan sheep (50), Ujimqin sheep (50), Hu sheep (50), Sunit sheep (50), Cele black sheep (50), Bayinbulak sheep (50 ), one month old.
[0051] The specific primers for SNP molecular markers are:
[0052] Forward primer: 5'-aatggggacacattttccaa-3'
[0053] Reverse primer: 5'-tggctcttggtgagtggtta-3'
[0054] (1) Collect 5 mL of anterior vena cava blood from sheep, and extract DNA by phenol-chloroform method;
[0055] (2) Using the genomic DNA of the sheep to be tested as a template, PCR amplification was carried out using specific primers marked by SNP molecules. The amplification system was shown in Table 3, and the amplification procedure was shown in Table 4 to obtain PCR products; El...
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