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Romaner007

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[求助] 关于甲基化PCR设计引物的问题,做这块的速来围观,给点指导!

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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具体是遇到什么问题了呢?可以加技术的Q:1951545998
016.艾德科技教你如何在线设计甲基化的引物  更多链接:http://www.aderr.com/cn/main.php ... 23&id=24445   
2楼2014-10-07 19:55:43
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