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Sample GSM1173153 Query DataSets for GSM1173153
Status Public on Jun 01, 2015
Title SC1X_LP-SC4B_LP
Sample type RNA
 
Channel 1
Source name SC1X_LP
Organism Daphnia pulex
Characteristics clone id: SC1X
genotype: ancient (~700-yr-old clone)
dietary group: LP (low P; C:P~120)
tissue: whole body
Growth protocol 20 C, 16:8 light: dark cycle, 1 mg C/L Scenedesmus algae at high or low phoshourus levels
Extracted molecule total RNA
Extraction protocol First, tissue is homogenized with Trizol Reagent (Ambion). Then RNA is extract with phenol and precipitated with Ethanol. The precipitate is captured and washed using Qiagen Rneasy spin column.
Label Cy3
Label protocol target protocol: Total RNA primed with T7-Oligo-dT and converted to aRNA using MessageAmpII aRNA Amplification Kit (Ambion) per manufacturer's recommnedations. aRNA primed with Random Hexamer Primer (Promega) and converted to ds cDNA using Double-stranded cDNA Synthesis Kit (Invitrogen). RNA degraded with RNaseA. ds cDNA purified with Invitrogen's ChargeSwitch Kit.
quality assessement protocol: Nanodrop ND-1000 (ThermoScientific) used to determine Total RNA concentrations. Bioanalyzer 2100 (Agilent Technologies) and RNA6000 Nano Kit (Agilent Technologies) used to determine Total RNA integrity. Nanodrop ND-1000 (ThermoScientific) used to determine aRNA concentrations. Bioanalyzer 2100 (Agilent Technologies) and RNA6000 Nano Kit (Agilent Technologies) used to determine aRNA integrity. Nanodrop ND-1000 (ThermoScientific) used to determine ds cDNA concentration. Bioanalyzer 2100 (Agilent Technologies) and DNA7500 Kit (Agilent Technologies) used to determine ds cDNA integrity.
ds cDNA labeled using NimbleGen Dual Color Labeling Kit (Roche NimbleGen) per manufacturer's recommendations. http://www.nimblegen.com
 
Channel 2
Source name SC4B_LP
Organism Daphnia pulex
Characteristics clone id: SC4B
genotype: contemporary (~10-yr-old clone)
dietary group: LP (low P; C:P~120)
tissue: whole body
Growth protocol 20 C, 16:8 light: dark cycle, 1 mg C/L Scenedesmus algae at high or low phoshourus levels
Extracted molecule total RNA
Extraction protocol First, tissue is homogenized with Trizol Reagent (Ambion). Then RNA is extract with phenol and precipitated with Ethanol. The precipitate is captured and washed using Qiagen Rneasy spin column.
Label Cy5
Label protocol target protocol: Total RNA primed with T7-Oligo-dT and converted to aRNA using MessageAmpII aRNA Amplification Kit (Ambion) per manufacturer's recommnedations. aRNA primed with Random Hexamer Primer (Promega) and converted to ds cDNA using Double-stranded cDNA Synthesis Kit (Invitrogen). RNA degraded with RNaseA. ds cDNA purified with Invitrogen's ChargeSwitch Kit.
quality assessement protocol: Nanodrop ND-1000 (ThermoScientific) used to determine Total RNA concentrations. Bioanalyzer 2100 (Agilent Technologies) and RNA6000 Nano Kit (Agilent Technologies) used to determine Total RNA integrity. Nanodrop ND-1000 (ThermoScientific) used to determine aRNA concentrations. Bioanalyzer 2100 (Agilent Technologies) and RNA6000 Nano Kit (Agilent Technologies) used to determine aRNA integrity. Nanodrop ND-1000 (ThermoScientific) used to determine ds cDNA concentration. Bioanalyzer 2100 (Agilent Technologies) and DNA7500 Kit (Agilent Technologies) used to determine ds cDNA integrity.
ds cDNA labeled using NimbleGen Dual Color Labeling Kit (Roche NimbleGen) per manufacturer's recommendations. http://www.nimblegen.com
 
 
Hybridization protocol Hybridization and post-hybridization washing using Hybridization Systems Kit (Roche NimbleGen) and Wash Buffer Kit (Roche NimbleGen) per manufacturer's recommendations. http://www.nimblegen.com
Scan protocol Image acquisition with Roche NimbleGen MS200 Scanner, 2 micron resolution.
Data processing Raw signal intensities extracted with NimbleScan 2.6 Software (Roche NimbleGen) as PAIR files.
 
Submission date Jun 24, 2013
Last update date Jun 01, 2015
Contact name Jacqueline Lopez
E-mail(s) jacqueline.ann.lopez@gmail.com
Phone 574-631-1902
Organization name University of Notre Dame
Department Biology
Lab Pfrender Laboratory
Street address 019 Galvin Life Science Center
City Notre Dame
State/province Indiana
ZIP/Postal code 46556
Country USA
 
Platform ID GPL11278
Series (1)
GSE48232 Identifying genes and pathways that respond differently to dietary C:P between old (~700-yr-old) and young (~10-yr-old) resurrected Daphnia pulicaria genotypes that differ in C and P physiology

Data table header descriptions
ID_REF
VALUE quantilie normalized, log2 ratio (Cy5/Cy3)

Data table
ID_REF VALUE
1000060_1_sc_30_1000060_1000180P00001 -0.127653320109426
100008_1_sc_67_100008_100137P00004 0.817991632773934
100009_3_1399871_1400680_1_SC13_1399882_1400677P00 1.06061047528507
100009_4_1403128_1403367_1_SC13_1403155_1403360P00 0.756985664793259
100009_5_1403624_1403706_1_SC13_1403624_1403706P00 0.0663295433894131
100010_1_sc_76_100010_100385P00154 0.398784877803447
1000131_1_sc_15_1000131_1000301P00033 0.00380308014618613
1000210_1_sc_8_1000216_1000403P00001 0.367722219418155
1000228_1_sc_5_1000228_1000303P00005 0.538498783318055
1000235_1_sc_12_1000235_1000385P00001 -0.5644809626407
1000302_1_sc_1_1000302_1002651P00649 0.453863181682058
1000302_2_sc_1_1000302_1002651P00020 -0.753133298160984
1000335_1_sc_24_1000335_1000630P00035 0.128560614825219
1000336_1_sc_4_1000336_1001676P00018 1.89784117994966
1000336_2_sc_4_1000336_1001676P00002 0.0270033577077342
1000336_4_sc_4_1000336_1001676P00001 0.0842154789662137
100034_1_sc_211_100034_100104P00001 -0.542686944961648
1000361_1_sc_15_1000361_1000506P00001 -0.0951632544869216
100036_2_1504384_1505256_1_SC13_1504408_1505253P00 -0.131908042189583
100036_3_1505325_1505953_1_SC13_1505355_1505953P00 -1.322633218132

Total number of rows: 134558

Table truncated, full table size 7764 Kbytes.




Supplementary file Size Download File type/resource
GSM1173153_540133_Cycle4_532.pair.gz 3.9 Mb (ftp)(http) PAIR
GSM1173153_540133_Cycle4_635.pair.gz 3.9 Mb (ftp)(http) PAIR
Processed data included within Sample table

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