Information about Samples:
Sample_titleleaf blade in WL, rep1leaf blade in WL, rep2leaf blade in WL, rep3leaf blade in D, rep1leaf blade in D, rep2leaf blade in D, rep3leaf blade in FRD, rep1leaf blade in FRD, rep2leaf blade in FRD, rep3petiole in WL, rep1petiole in WL, rep2petiole in WL, rep3petiole in D, rep1petiole in D, rep2petiole in D, rep3petiole in FRD, rep1petiole in FRD, rep2petiole in FRD, rep3
Sample_geo_accessionGSM445710GSM445711GSM445712GSM445713GSM445714GSM445715GSM445716GSM445717GSM445718GSM445719GSM445720GSM445721GSM445722GSM445723GSM445724GSM445725GSM445726GSM445727
Sample_typeRNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNARNA
Sample_channel_count111111111111111111
Sample_source_name_ch1leaf blade in WLleaf blade in WLleaf blade in WLleaf blade in Dleaf blade in Dleaf blade in Dleaf blade in FRDleaf blade in FRDleaf blade in FRDpetiole in WLpetiole in WLpetiole in WLpetiole in Dpetiole in Dpetiole in Dpetiole in FRDpetiole in FRDpetiole in FRD
Sample_organism_ch1Arabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thalianaArabidopsis thaliana
Sample_characteristics_ch1tissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: leaf bladestissue: petiolestissue: petiolestissue: petiolestissue: petiolestissue: petiolestissue: petiolestissue: petiolestissue: petiolestissue: petioles
Sample_treatment_protocol_ch1Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).Seedlings were either treated with white light for 2 h (WL), incubated in the dark condition for 2 h (D), or pulse irradiation of FR light before incubated in the dark condition for 2 h (FRD).
Sample_growth_protocol_ch1Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.Seedlings were grown at 22 degrees on rocklwools under continuous white light for 19 days.
Sample_molecule_ch1total RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNAtotal RNA
Sample_extract_protocol_ch1Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.Total RNA was separately prepared from leaf blades and petioles using Sepazol RNA I super kit (Nacalai Tesque), and purified with RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.
Sample_label_ch1BiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotinBiotin
Sample_label_protocol_ch1Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.Followed Affymetrix experimental procedure. Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 microg total RNA.
Sample_taxid_ch1370237023702370237023702370237023702370237023702370237023702370237023702
Sample_hyb_protocolFollowed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.Followed Affymetrix experimental procedure. 200 micro liter of hybrization solution was used for 16 hrs at 45°C.
Sample_scan_protocolGeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).GeneChips were scanned using the Gene Array Scanner (Agilent).
Sample_descriptionThe 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.The 3rd and 4th rosette leaves were used.
Sample_platform_idGPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198GPL198