Are seeds suitable for flow cytometric estimation of plant genome size?

Cytometry Part A

Volumn 64, Issue 2, 2005, Pages 72-79

  Sliwinska, Elwira ^a   Zielinska, Elzbieta ^a,b   Jedrzejczyk, Iwona ^a  

^a UNIVERSITY OF TECHNOLOGY AND LIFE SCIENCES   (Poland)

^b WARSAW UNIVERSITY OF LIFE SCIENCES   (Poland)

Author keywords

Anethum graveolens; Beta vulgaris; Brassica napus var. oleifera; DNA content; Flow cytometry; Helianthus annuus; Pisum sativum; Staining inhibitors; Zea mays

Indexed keywords

BUFFER; CELL NUCLEUS DNA; FLUOROCHROME; PROPIDIUM IODIDE; REDUCING AGENT;

ARTICLE; BEET; CELL CYCLE G0 PHASE; CELL CYCLE G1 PHASE; CELL NUCLEUS; COST; CYTOSOL; DILL; DNA CONTENT; ENDOSPERM; FLOW CYTOMETRY; GENOME SIZE; INTERCALATION COMPLEX; ISOLATION PROCEDURE; MAIZE; MEASUREMENT; MITOSIS INHIBITION; NONHUMAN; PEA; PLANT GROWTH; PLANT SEED; PRIORITY JOURNAL; RAPESEED; SEEDLING; SUNFLOWER; TISSUE SPECIFICITY;

ANETHUM GRAVEOLENS; BETA VULGARIS; BRASSICA NAPUS; CELL NUCLEUS; DNA, PLANT; FLOW CYTOMETRY; GENOME, PLANT; HELIANTHUS; PEAS; PLANT LEAVES; PLANTS; PLOIDIES; PROPIDIUM; SEEDS; ZEA MAYS;

EID: 17044402106     PISSN: 15524922     EISSN: None     Source Type: Journal    
DOI: 10.1002/cyto.a.20122     Document Type: Article

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