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1 issolution in a mixture of sulfuric acid and sodium bisulfite.
2 96-residue-long C-terminal part of D2) with sodium bisulfite.
3 atment of the palindrome-containing DNA with sodium bisulfite at high temperature results in deaminat
6 om primary chicken erythroid cells using the sodium bisulfite conversion technique and found all CpGs
8 assay entails initial modification of DNA by sodium bisulfite, converting all unmethylated, but not m
13 on involve the treatment of genomic DNA with sodium bisulfite; however, this method cannot distinguis
16 hylation-sensitive SSCP (Ms-SSCP) technique, sodium bisulfite modification of DNA converts unmethylat
18 all cytosines were converted to thymidine by sodium bisulfite mutagenesis, indicating that none of th
20 rom HCT116 cells and analysis of genome-wide sodium bisulfite sequencing data sets from several other
21 ethylation status of proximal GC boxes using sodium bisulfite sequencing reveals differential methyla
27 al reaction of gDNA with concentrated acidic sodium bisulfite to quantitatively convert C to uracil (
28 more, unbiased next-generation sequencing of sodium bisulfite treated total DNA from HCT116 cells and
29 dent sequence differences in PCR products of sodium bisulfite-treated DNA as described previously.
30 ymerase chain reaction and sequencing of the sodium bisulfite-treated DNA from HCC cell lines and HCC
32 lation-specific PCR and sequence analysis of sodium bisulfite-treated genomic DNA, we demonstrate a s
37 oportions of the C/T polymorphism induced by sodium bisulfite treatment of DNA reflects the DNA methy
40 ical fo r functional photosystem II (PS II), sodium bisulfite was utilized for in vitro random mutage
41 f methylated and unmethylated cytosines with sodium bisulfite, which exclusively converts unmethylate
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