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Genomic DNA was extracted from the leaf tissues of a single plant from each accession using the MATAB method described in Risterucci et al. (2000) and then diluted to 100 ng/μl.
Thus, the similarities of PC1 scores in DNA methylation from two different tissues of a single individual are specific.
All FLcDNA libraries were made from insect-induced tissues of a single Sitka spruce genotype (Table 1).
Figure 2b shows the relative abundances among the transcripts of the three tissues of a single individual.
Genomic DNA was extracted from the leaf tissues of a single danshen plant using the cetyltrimethylammonium bromide (CTAB) method.
RNA was extracted from the tissues of a single individual (Tri-reagent, Sigma-Aldrich) and reverse transcribed (Superscript III, Invitrogen).
Similar(45)
DNA (2.5 µg), extracted from leaf tissue of a single N. caerulescens plant via the phenol – chloroform procedure [49], was randomly sheared to 40 kb fragments and end repaired to blunt, 5'-phosphorylated 5'-phosphorylated
Briefly, the gill tissue of a single individual was ground in a glass tissue homogenizer and frozen until further processing.
Most of the sequence data were derived from whole-genome shotgun sequencing of a single megagametophyte, the haploid tissue of a single pine seed.
Whole genomic DNA was extracted from muscle tissue of a single H. abdominalis individual using a standard proteinase K/phenol-chloroform protocol [ 53].
The fifth sample (sample ID n24h-4) was derived from tissue of a single untreated quarter since the noninfected udder quarters of this cow differed in somatic cells counts.
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