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Bisulfite conversion of genomic DNA for methylation Examination: protocol simplification with larger recovery relevant to constrained samples and improved throughput

Bisulfite genomic sequencing will be the most generally employed technique to research the 5-methylation of cytosines, the widespread covalent DNA modification in mammals. The process relies around the selective transformation of unmethylated cytosines to uridines. Then, the investigated genomic areas are PCR amplified, subcloned and sequenced. In the course of sequencing, the at first unmethylated cytosines are detected as thymines. The efficacy of bisulfite PCR is generally small; mispriming and non-precise amplification typically occurs because of the T richness of the goal sequences.

Protein sequences, three-D structures, and resources website to the review of useful protein domains and Lively sites

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