2009
DOI: 10.1016/j.scienta.2008.09.020
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Detection of somaclonal variation in micro-propagated Echinacea purpurea using AFLP marker

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Cited by 38 publications
(24 citation statements)
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“…The reasons accounting for somaclonal variations remain unclear, although factors such as culture duration, number of subcultures or transfers (Borse et al, 2011), phytoregulators (Biswas et al, 2009), explant type (Chuang et al, 2009), passage through the indirect callus phase (mass of undifferentiated cells with regeneration potential) (Peredo et al, 2006), genotype (Khan et al, 2009), culture medium composition (Lutts et al, 1998), and ploidy and mosaicism levels (Nakano et al, 2006) are considered capable of inducing this variability in vitro.…”
Section: Resultsmentioning
confidence: 99%
“…The reasons accounting for somaclonal variations remain unclear, although factors such as culture duration, number of subcultures or transfers (Borse et al, 2011), phytoregulators (Biswas et al, 2009), explant type (Chuang et al, 2009), passage through the indirect callus phase (mass of undifferentiated cells with regeneration potential) (Peredo et al, 2006), genotype (Khan et al, 2009), culture medium composition (Lutts et al, 1998), and ploidy and mosaicism levels (Nakano et al, 2006) are considered capable of inducing this variability in vitro.…”
Section: Resultsmentioning
confidence: 99%
“…Genomic DNA of each accession was extracted from freshly harvested young leaves by using CTAB (hexadecyltrimethylammonium bromide) procedure described by Chuang et al (2009). The samples of bulked leaf tissues (500 mg) collected from five individual plants were used for DNA extraction.…”
Section: Methodsmentioning
confidence: 99%
“…The explant tissue can affect the frequency and nature of somaclonal variation [38,39]. The use of meristematic tissues, such as the pericycle, procambium and cambium, as starting materials for tissue culture reduces the possibility of variation [40].…”
Section: Explant Sourcementioning
confidence: 99%