Information about Samples:
Sample_titleWT_3h_+P_rep1WT_3h_+P_rep2WT_3h_+P_rep3pnp1-1_3h_+P_rep1pnp1-1_3h_+P_rep2pnp1-1_3h_+P_rep3WT_3h_-P_rep1WT_3h_-P_rep2WT_3h_-P_rep3pnp1-1_3h_-P_rep1pnp1-1_3h_-P_rep2pnp1-1_3h_-P_rep3WT_1wk_+P_rep1WT_1wk_+P_rep2WT_1wk_+P_rep3pnp1-1_1wk_+P_rep1pnp1-1_1wk_+P_rep2pnp1-1_1wk_+P_rep3WT_1wk_-P_rep1WT_1wk_-P_rep2WT_1wk_-P_rep3pnp1-1_1wk_-P_rep1pnp1-1_1wk_-P_rep2pnp1-1_1wk_-P_rep3
Sample_geo_accessionGSM451826GSM451827GSM451828GSM451829GSM451830GSM451831GSM451832GSM451833GSM451834GSM451835GSM451836GSM451837GSM451838GSM451839GSM451840GSM451841GSM451842GSM451843GSM451844GSM451845GSM451846GSM451847GSM451848GSM451849
Sample_typeRNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNA
Sample_channel_count111111111111111111111111
Sample_source_name_ch12-week old WT rosette grown for 3 additional hours on +P medium2-week old WT rosette grown for 3 additional hours on +P medium2-week old WT rosette grown for 3 additional hours on +P medium2-week old pnp1-1 rosette grown for 3 additional hours on +P medium2-week old pnp1-1 rosette grown for 3 additional hours on +P medium2-week old pnp1-1 rosette grown for 3 additional hours on +P medium2-week old WT rosette grown for 3 additional hours on -P medium2-week old WT rosette grown for 3 additional hours on -P medium2-week old WT rosette grown for 3 additional hours on -P medium2-week old pnp1-1 rosette grown for 3 additional hours on -P medium2-week old pnp1-1 rosette grown for 3 additional hours on -P medium2-week old pnp1-1 rosette grown for 3 additional hours on -P medium2-week old WT rosette grown for one additional week on +P medium2-week old WT rosette grown for one additional week on +P medium2-week old WT rosette grown for one additional week on +P medium2-week old pnp1-1 rosette grown for one additional week on +P medium2-week old pnp1-1 rosette grown for one additional week on +P medium2-week old pnp1-1 rosette grown for one additional week on +P medium2-week old WT rosette grown for one additional week on -P medium2-week old WT rosette grown for one additional week on -P medium2-week old WT rosette grown for one additional week on -P medium2-week old pnp1-1 rosette grown for one additional week on -P medium2-week old pnp1-1 rosette grown for one additional week on -P medium2-week old pnp1-1 rosette grown for one additional week on -P medium
Sample_organism_ch1Arabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thaliana
Sample_characteristics_ch1tissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without rootstissue: seedlings without roots
Sample_characteristics_ch1age: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 2 weeks + 3hage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeksage: 3 weeks
Sample_characteristics_ch1genotype: WT Col0genotype: WT Col0genotype: WT Col0genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: WT Col0genotype: WT Col0genotype: WT Col0genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: WT Col0genotype: WT Col0genotype: WT Col0genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: WT Col0genotype: WT Col0genotype: WT Col0genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)genotype: pnp1-1 (SALK_013306)
Sample_characteristics_ch1treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: Full nutrient medium (+P)treatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate mediumtreatment: No phosphate medium
Sample_treatment_protocol_ch1After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.After two weeks, they were transferred to fresh +P or -P MS medium. For the -P medium, KH2PO4 was omitted but the potassium was compensated by K2SO4. Plantlets were rinsed with distilled water before transfer and then grown for 3h or one week.
Sample_growth_protocol_ch1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1WT and pnp1-1 plants (Columbia -0) were germinated and grown for 2 weeks on a full nutrient MS medium (+P) containing 0.6% phytagar (w/v) and 0.5% (w/v) Suc at 22˚C in a growth chamber under a 16-h photoperiod (with a fluorescent light intensity of 200 μmol m-2 s-1
Sample_molecule_ch1total RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNA
Sample_extract_protocol_ch1Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.Total RNA was isolated from seedlings, from which roots had been removed, using the RNeasy Plant Minikit (Qiagen), including DNase treatment according to the manufacturer’s instructions.
Sample_label_ch1biotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotinbiotin
Sample_label_protocol_ch1One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.One microgram of each total RNA sample was labeled using MessageAmp™ II-Biotin /Enhanced/ Single Round aRNA Amplification Kit from Ambion (Austin, TX), according to manufacture provided protocol.
Sample_taxid_ch1370237023702370237023702370237023702370237023702370237023702370237023702370237023702370237023702
Sample_hyb_protocolLabeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).Labeled cRNA was hybridized on Affymetrix Arabidopsis ATH1 Genome arrays, stained and washed according to standard protocol by Affymetrix (Santa Clara, CA).
Sample_scan_protocolGeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.GeneChips were scanned using the and scanned by GeneChip Scanner 3000.
Sample_descriptionWT_3h_+P_rep1WT_3h_+P_rep2WT_3h_+P_rep3pnp1-1_3h_+P_rep1pnp1-1_3h_+P_rep2pnp1-1_3h_+P_rep3WT_3h_-P_rep1WT_3h_-P_rep2WT_3h_-P_rep3pnp1-1_3h_-P_rep1pnp1-1_3h_-P_rep2pnp1-1_3h_-P_rep3WT_1wk_+P_rep1WT_1wk_+P_rep2WT_1wk_+P_rep3pnp1-1_1wk_+P_rep1pnp1-1_1wk_+P_rep2pnp1-1_1wk_+P_rep3WT_1wk_-P_rep1WT_1wk_-P_rep2WT_1wk_-P_rep3pnp1-1_1wk_-P_rep1pnp1-1_1wk_-P_rep2pnp1-1_1wk_-P_rep3
Sample_platform_idGPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198