NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM244717 Query DataSets for GSM244717
Status Public on Nov 15, 2008
Title Leaves-Wild type rep.1
Sample type RNA
 
Source name first two leaves of 10 day old light grown in vitro seedlings
Organism Solanum lycopersicum
Characteristics First two leaves of tomato seedlings grown in light conditions -Wild type
Treatment protocol No special treatments before harvesting were carried out.
Growth protocol For fruits, tomato plants were grown in pots with growing medium containing 50% of sand and 50% of Sun Gro Redi-earth Plug and Seedling Mix (Sun Gro Horticulture). All plants grown in growth chamber of Phytotron, NCSU at day temperature 26 C, night temperature 22 C, humidity 45% and intensity of light 500 μmol.m-2.s-1. Plants were watered once at day to field capacity and fertilized on a weekly basis with fertilizer recipe as described at http://www.ncsu.edu/phytotron/manual.pdf. After 9 weeks in the growth chamber transgenic and control ripe fruits of same age were harvested.
For leaves, tomato seeds were germinated on MS medium (agar Petri plates) in light conditions. First two leaves of 10 days seedlings were harvested.
For roots, tomato seeds were germinated on MS medium (agar Petri plates) in light conditions. First two leaves of 10 days seedlings were harvested.
Extracted molecule total RNA
Extraction protocol Ripe fruits were immediately frozen in liquid nitrogen after harvesting in the greenhouses. The harvested samples were then transferred to the laboratory and grinded to a fine powder in mortars and pestles using liquid nitrogen. Total RNA was extracted using a RNeasy Plant Mini Kit (Qiagen).
Leaf tissue was immediately frozen in liquid nitrogen after harvesting in the sterile conditions. The harvested leaf samples were then transferred to the laboratory and grinded to a fine powder in mortars and pestles using liquid nitrogen. Total RNA was
Root tips were isolated from rootsand immediately frozen in liquid nitrogen after harvesting in the dark conditions. The harvested root samples were then transferred to the laboratory and grinded to a fine powder in mortars and pestles using liquid nitro
Label biotin
Label protocol Complimentary RNA (cRNA) was produced according to Affymetrix Eukaryotic two-cycle target labeling assay as specified in the GeneChip Expression Analysis Technical Manual (http://www.affymetrix.com/support/technical/manual/expression_manual.affx).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Tomato Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400. Hybridization reactions to Affymetrix Maize GeneChip expression arrays were done using the services of Expression Analysis Inc. (http://www.expressionanalysis.com/).
Scan protocol Scanning of the Affymetrix Tomato GeneChip expression arrays were done using the services of Expression Analysis Inc. (http://www.expressionanalysis.com/).
Description Gene expression data from first two leaves of tomato seedlings grown in vitro in light conditions
Data processing Data extraction was also performed by Expression Analysis Inc. Expression values were calculated using the Affymetrix GeneChip Operating System (GCOS) and were based on the difference of the PM (Perfect Match) signal and MM (Mismatch) signal at each of the probe pairs. The fluorescent signal values from each array were normalized to achieve similar overall intensity between arrays. The fluorescent signal values of any hybridization reaction were then multiplied by a scaling factor to make their (trimmed) mean intensity equal to 500. The scaling factor is unique to each hybridization reaction and is in general below 10
 
Submission date Nov 26, 2007
Last update date Aug 14, 2011
Contact name Mariya Khodakovskaya
E-mail(s) mvkhodak@ncsu.edu
Phone 919-515-2225
Fax 919-515-3436
Organization name North Carolina State University
Department Plant Biology
Lab Plant Sensory Genomics Group
Street address 4218 Gardner Hall
City Raleigh
State/province NC
ZIP/Postal code 27695
Country USA
 
Platform ID GPL4741
Series (1)
GSE9683 Tomato wild type, vector control and transgenic lines expressing InsP 5-ptase: mature fruits, root tips, and leaves

Data table header descriptions
ID_REF
VALUE MAS5.0-calculated signal intensity
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 112.874 P 0.000296708
AFFX-BioB-M_at 132.636 P 5.16732e-05
AFFX-BioB-3_at 122.606 P 4.42873e-05
AFFX-BioC-5_at 419.38 P 4.42873e-05
AFFX-BioC-3_at 386.818 P 4.42873e-05
AFFX-BioDn-5_at 891.74 P 4.42873e-05
AFFX-BioDn-3_at 1414.66 P 4.42873e-05
AFFX-CreX-5_at 3707.62 P 5.16732e-05
AFFX-CreX-3_at 4633.39 P 4.42873e-05
AFFX-DapX-5_at 66.6475 P 0.000169227
AFFX-DapX-M_at 1195.17 P 4.42873e-05
AFFX-DapX-3_at 3591.93 P 4.42873e-05
AFFX-LysX-5_at 37.9078 P 0.000195116
AFFX-LysX-M_at 226.879 P 4.42873e-05
AFFX-LysX-3_at 937.706 P 5.16732e-05
AFFX-PheX-5_at 62.7558 P 4.42873e-05
AFFX-PheX-M_at 314.497 P 4.42873e-05
AFFX-PheX-3_at 806.384 P 4.42873e-05
AFFX-ThrX-5_at 25.2328 P 0.00359458
AFFX-ThrX-M_at 216.618 P 4.42873e-05

Total number of rows: 10209

Table truncated, full table size 396 Kbytes.




Supplementary file Size Download File type/resource
GSM244717.CEL.gz 952.6 Kb (ftp)(http) CEL
GSM244717.CHP.gz 54.2 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap