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  1. .... Overall, our data demonstrate that bisulfite-PCR/LDR/Universal Array approach is a quantitative and sensitive method for the measurement of DNA methylation. View larger version: In this window In a new window Figure 3. The quantification curves of the assay. Genomic DNAs of HCT15 and normal human...
  2. ...the development of a homogeneous DNA detection method that requires no further manipulations after the initial reaction is set up. This assay, named dye-labeled oligonucleotide ligation (DOL), combines the PCR and the oligonucleotide ligation reaction in a two-stage thermal cycling sequence with fluorescence...
  3. ...subclonal cultures representing individual lineages. From our time-lapse data, we were able to measure the inter-division times for all cells in the device. We extracted genomic DNA from subclones and prepared PCR-free shotgun sequence libraries, which were sequenced to 35-fold coverage (Methods...
  4. ...isolation of the DNA and proteins.SURVEYOR nuclease assay and Western blotThe DNA fragments of the AASV1 locus were amplified from extracted genomic DNA by PCR using the Q5 high-fidelity DNA polymerases (NEB). SURVEYOR nuclease assays were subsequently performed according to the manufacturer's instructions...
  5. ...is shown as reference for view of fluorescence image. Nepal et al . 1944 Genome Research www..org These data, together with the independent developmental dynamics, cDNA alignment, and reporter gene functional assays, argue that exon and intron 59- and 39-end associated RNAs are biochemically independent...
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