2001
DOI: 10.1590/s0100-29452001000200051
|View full text |Cite
|
Sign up to set email alerts
|

EXTRAÇÃO DE DNA GENÔMICO DE Passiflora spp. PARA ANÁLISES PCR-RAPD

Abstract: A identificação e caracterização da diversidade genética de plantas por meio de técnicas moleculares envolvem a avaliação de vários indivíduos, necessitando-se, portanto, de métodos rápidos e precisos de extração do DNA. O co-isolamento de polissacarídeos, fenóis e compostos secundários é o principal problema encontrado no isolamento e purificação de DNA vegetal. Folhas das diversas espécies de Passiflora possuem níveis variados desses compostos que podem comprometer este procedimento. O presente estudo foi re… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
7
0
5

Year Published

2003
2003
2021
2021

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 13 publications
(12 citation statements)
references
References 7 publications
0
7
0
5
Order By: Relevance
“…Leaves of two plants from each accession were collected to extract the genomic DNA by the CTAB method according to Molinari & Crochemore (2001). Fresh plant tissue was macerated with a glass bar.…”
Section: Methodsmentioning
confidence: 99%
“…Leaves of two plants from each accession were collected to extract the genomic DNA by the CTAB method according to Molinari & Crochemore (2001). Fresh plant tissue was macerated with a glass bar.…”
Section: Methodsmentioning
confidence: 99%
“…The leaves were oven-dried (37ºC) for 12 h and then macerated until a fine dust. DNA extraction was performed as described by Molinari and Crochemore (2001). DNA concentration was estimated in a fluorimeter as described by the manufacturer (Hoefer Scientific Instruments).…”
Section: Dna Extractionmentioning
confidence: 99%
“…Moreover, the method is less laborious and safer, since 2-mercaptoethanol was eliminated from this protocol. 2-Mercaptoethanol is volatile and toxic and requires additional care when handled (Molinari and Crochemore, 2001;Sambrook and Russel, 2001). …”
Section: Resultsmentioning
confidence: 99%
“…Most of all, the impurities can interfere in the action of restriction enzymes, Taq polymerase in PCR reactions or electrophoretic separation of DNA fragments (Molinari and Crochemore, 2001). An efficient protocol for DNA isolation provides good conditions for PCR amplification allowing reproducibility and clear bands.…”
Section: Introductionmentioning
confidence: 99%