2011
DOI: 10.1016/j.scienta.2011.09.001
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Isolation and expression pattern of genes related to flower initiation in the evergreen azalea, Rhododendron×pulchrum ‘Oomurasaki’

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Cited by 21 publications
(18 citation statements)
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“…Quantitation was performed by using the difference in the threshold cycle values (ΔCt) between the two samples (the target genes and the reference genes, both azalea ACTIN and Histone H3) to calculate the relative amounts of the template present. The value of the relative expression was calculated as the standard using the maximum value for the RoPI gene, and the mean and standard error (SE) were calculated from the value of the relative expression (Cheon et al, 2011).…”
Section: Expression Analysis Of Kurume Azalea Pi/glo Homologmentioning
confidence: 99%
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“…Quantitation was performed by using the difference in the threshold cycle values (ΔCt) between the two samples (the target genes and the reference genes, both azalea ACTIN and Histone H3) to calculate the relative amounts of the template present. The value of the relative expression was calculated as the standard using the maximum value for the RoPI gene, and the mean and standard error (SE) were calculated from the value of the relative expression (Cheon et al, 2011).…”
Section: Expression Analysis Of Kurume Azalea Pi/glo Homologmentioning
confidence: 99%
“…In contrast to other plants, floral form mutations in azaleas have been poorly investigated at the molecular level. After initiation of floral bud formation, RpAP3 expression was increased in the floral buds of Rhododendron × pulchrum (Cheon et al, 2011), and RkAG was overexpressed in the second whorl of staminoid-petaled cultivars of R. kaempferi (Tasaki et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…The primer pairs used for the RT-qPCR assay were reported previously (Cheon et al, 2011(Cheon et al, , 2012. In the RT-qPCR assay, 0.5 μl of the cDNA samples was used as the template in a 20 μl RT-qPCR assay mix containing 10 μl SYBR Premix Ex Taq II (TaKaRa Bio) and 0.25 μM of each primer.…”
Section: Rna Extraction and Cdna Synthesismentioning
confidence: 99%
“…Each stage of floral organ formation was collected on 24 July and 7 August. RT-qPCR was performed with gene-specific primers (Cheon et al, 2011(Cheon et al, , 2012. Data are the mean ± SE (n = 3; normalized against both Histone H3 and ACTIN).…”
Section: Observation Of Floral Organ Developmentmentioning
confidence: 99%
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