Specific primer and parting method for II-type MHC gene for anti-bacterial potential detection on crested ibis
A typing method and genotyping technology, which can be applied to biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. question
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example 1
[0043] 1. Sample preparation: Crested ibis blood and tissue samples came from artificial populations such as Deqing, Sado, Beijing, Henan, Yangxian and Louguantai.
[0044]2. DNA extraction: phenol chloroform method to extract blood and tissue DNA.
[0045] 3. Primer synthesis: According to the obtained crested ibis class II-MHC gene sequence, specific primers for the II-A1 site were designed to amplify exon 2 for genotyping of the modified site, and BGI synthesized primers. The primer sequences are as follows:
[0046]
[0047] 4. Primer amplification: apply the above amplification primers to PCR respectively to amplify the extracted sample DNA. Set the PCR thermal cycle annealing temperature range to 64°C.
[0048] 5. Amplification result detection: take 2 ul of the above-mentioned PCR amplification products and carry out agarose gel electrophoresis, the gel concentration is 1.5%. The result is as figure 1 As shown, this primer can effectively amplify the target band,...
example 2
[0062] 1. Sample preparation: Crested ibis blood and tissue samples came from artificial populations such as Deqing, Sado, Beijing, Henan, Yangxian and Louguantai.
[0063] 2. DNA extraction: phenol chloroform method to extract blood and tissue DNA.
[0064] 3. Primer synthesis: According to the obtained crested ibis class II MHC gene sequence, specific primers for the II-B1 site were designed to amplify exon 2, and the primers were synthesized by BGI. The primer sequences are as follows:
[0065]
[0066] 4. Primer amplification: apply the above amplification primers to PCR respectively to amplify the extracted sample DNA. Set the PCR thermal cycle annealing temperature range to 63°C.
[0067] 5. Amplification result detection: take 2 ul of the above-mentioned PCR amplification products and carry out agarose gel electrophoresis, the gel concentration is 1.5%. The result is as figure 2 As shown, this primer can effectively amplify the target band, the fragment size of ...
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