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SRX1744808: Ruveia_undamaged
1 LS454 (454 GS FLX Titanium) run: 146,765 spots, 79.8M bases, 178.5Mb downloads

Design: Total RNA was extracted from 200 mg of olive mesocarp with RNeasy Plant Mini Kit (Qiagen Hilden, Germany) and treated with DNase I (Ambion, Austin, TX, USA). Three biological replicates consisting of 5 olives each were used for each biological condition (control undamaged olives). cDNAs were synthesized using the SMART PCR cDNA Synthesis kit (Clontech, Palo Alto, CA, USA). First strand synthesis was performed using 8 µg of total RNA, as described by Alagna et al. (2009). Double stranded cDNAs were purified using the QIAquick PCR purification kit (Qiagen, Hilden, Germany) and quantified with a fluorimeter (Victor 2, Perkin Elmer, Wellesley, MA, USA). To verify the cDNA quality and fragment length, all samples were separated on a 1.5% agarose gel.
Submitted by: ENEA
Study: Olea__bactrocera
show Abstracthide Abstract
Pyrosequencing of four cDNA libraries from damaged (pool of different stages of fly attack) and control undamaged fruits of ‘Ortice’ and ‘Ruveia’ (Olea europaea L.), characterized by a different tolerance to Bactrocera oleae, generated a comprehensive repertory of transcripts useful to study the genes modulated by Bactrocera oleae attack.
Sample: Ruveia_undamaged
SAMN04957804 • SRS1423869 • All experiments • All runs
Organism: Olea europaea
Library:
Instrument: 454 GS FLX Titanium
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: unspecified
Layout: SINGLE
Spot descriptor:
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Runs: 1 run, 146,765 spots, 79.8M bases, 178.5Mb
Run# of Spots# of BasesSizePublished
SRR3479026146,76579.8M178.5Mb2017-05-06

ID:
2502325

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