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Romaner007金蟲 (小有名氣)
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[求助]
關于甲基化PCR設計引物的問題,做這塊的速來圍觀,給點指導!
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TATAACATTTAACCCTGGTCAGGTTGCTAGGTCATATATTTTGTGTTTCCTTTCTCGGCCGGCCTGCGGCGGCGGCAGCGGCGGCGTTTCTCGCCTCCTCTTCGTCTTTTCTAACCGTGCAGCCTCTTCCTAGGCTTCTCCTGAAAGGGAAGGTGGAAGCCGTGGGCTCGGGCGGGAGCCGGCTGAGGCGCGGCGGCGGCGGCGGCACCTCCCGCTCCTGGAGCGGGGGGGAGAAGCGGCGGCGGCGGCGGCCGCGGCGGCTGCAGCTCCAGGGAGGGGGTCTGAGTCGCCTGTCACCATTTCCAGGGCTGGGAACGCCGGAGAGTTGGTCTCTCCCCTTCTACTGCCTCCAACACGGCGGCGGCGGCGGCTGGCACATCCAGGGACCCGGGCCGGTTTTAAACCTCCCGTGCGCCGCCGCCGCACCCCCCGTGGCCCGGGCTCCGGAGGCCGCCGGCGGAGGCAGCCGTTCGGAGGATTATTCGTCTTCTCCCCATTCCGCTGAAGCTGCTGCCAGGCCTCTGGCTGCTGAGGAGAAGCAGGCCCAGTCGCTGCAACCATCCAGCAGCC Blue CG is a potential site of mythelation in promotor region of gene X101. When the promotor DNA was treated with bisulfite, please design primers that should be as described below: 1. Confirm the site methylated or unmethylated with site-specific PCR. 2. PCR result is positive when the Blue CG is methylated. 3. PCR result is positive when the Blue CG is unmethylated. 4. PCR product will be 400 bp at length on agarose gel. 5. 20-21 bp of primers will be synthesized commercially. |

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具體是遇到什么問題了呢?可以加技術的Q:1951545998 016.艾德科技教你如何在線設計甲基化的引物 更多鏈接:http://www.aderr.com/cn/main.php ... 23&id=24445 |
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