1992
DOI: 10.1093/oxfordjournals.aob.a088335
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Flow Cytometric Determination of Nuclear Replication Stages in Tomato Seeds during Priming and Germination

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Cited by 120 publications
(85 citation statements)
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“…Flow cytometry was performed according to a protocol modified from Bino et al (1992), and Arumuganathan and Earle (1991) on a BD Biosciences FACSCalibur flow cytometer (BD Biosciences, San Jose, CA, USA), using three to five young leaves per plant (approx. 15-20 mm in length, resulting in approximately 70 mg of tissue) stained with propidium iodide.…”
Section: Dna Contentmentioning
confidence: 99%
“…Flow cytometry was performed according to a protocol modified from Bino et al (1992), and Arumuganathan and Earle (1991) on a BD Biosciences FACSCalibur flow cytometer (BD Biosciences, San Jose, CA, USA), using three to five young leaves per plant (approx. 15-20 mm in length, resulting in approximately 70 mg of tissue) stained with propidium iodide.…”
Section: Dna Contentmentioning
confidence: 99%
“…Osmotic priming was carried out on top of filter paper soaked with 30% (w/v) PEG-6000 (-1.0 MPa) in a sealed Petri dish from 6 h to a maximum of 7 d at 20°C in darkness (Bino et al, 1992). After priming, seeds were washed for 5 min under running tap water to remove PEG from the seed coat.…”
Section: Priming Aging and Lmbibition Conditionsmentioning
confidence: 99%
“…and pepper (Capsicurn annuum L.), imbibition is coupled to initiation of DNA replication in cells of the embryo root tip, as was demonstrated by flow cytometric analysis of isolated nuclei (Bino et al, 1992;Lanteri et al, 1993). In these species, the embryonic cells progress through the S phase of the cell cycle into the G, phase before visible germination.…”
mentioning
confidence: 98%
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