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Isolation of plant DNA from fresh tissue

Jeff J. Doyle
- Vol. 12, pp 13-15
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The article was published on 1990-01-01 and is currently open access. It has received 10843 citations till now. The article focuses on the topics: Fresh Tissue.

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Universal primers for amplification of three non-coding regions of chloroplast DNA

TL;DR: Six primers for the amplification of three non-coding regions of chloroplast DNA via the polymerase chain reaction (PCR) have been designed and worked for most species tested, which means that they may be used to study the population biology and evolution of plants.
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Genetic linkage maps of Eucalyptus grandis and Eucalyptus urophylla using a pseudo-testcross: mapping strategy and RAPD markers

TL;DR: The combined use of RAPD markers and the pseudo-testcross configuration is proposed as a general strategy for the construction of single individual genetic linkage maps in outbred forest trees as well as in any highly heterozygous sexually reproducing living organisms.
Journal ArticleDOI

A set of universal primers for amplification of polymorphic non‐coding regions of mitochondrial and chloroplast DNA in plants

TL;DR: The genetic information present in the plant mitochondrial DNA and chloroplast DNA is of great interest in phylogeny and in population genetics, largely because of the non-mendelian mode of inheritance of these genomes.
Journal ArticleDOI

A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae

TL;DR: PHR1-binding sequences are present in the promoter of Pi starvation-responsive structural genes, indicating that this protein acts downstream in the Pi starvation signaling pathway.
Journal ArticleDOI

PCR-amplified microsatellites as markers in plant genetics.

TL;DR: Polymerase chain reaction amplification of ( AT)n and (TAT)n microsatellites in soybean revealed that they are highly polymorphic, as a consequence of length variation, somatically stable and inherited in a co-dominant Mendelian manner.
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