Gene Expression Omnibus (GEO) Overview Version:2014-04-12Japanese page
An overview of the GEO entries broken down by the measurement platforms and the features of the measured samples.
RSS
Data Unit : [ DataSet / Sample / Platform ] Show explanation>> <<Hide explanation
DataSet : Series(GSE) x Platform(GPL). A set of related gene expression data.
Sample : Biological materials.
platform : Methods or instruments used for the gene expression profilings.
The numbers shown in the tabs are the numbers of the data (series, samples or platforms) belonging to the groups.
  Human
(4,712)
  Primates
(41)
  Rodents
(1,963)
  Mammals
(85)
  Vertebrates
(71)
  Invertebrates
(162)
  Plants
(837)
  Bacteria
(313)
  Viruses
(0)
  Phages
(18)
  Unclassified
(320)
  All
(8,522)
 
  SAGE NlaIII
(26)
  SAGE RsaI
(0)
  SAGE Sau3A
(0)
  MPSS
(9)
  GeneChip
(3,922)
  Tiling Array
(244)
  cDNA Array
(2,494)
  Oligo Array
(1,459)
  Bead Array
(334)
  Protein Array
(0)
  Antibody
(0)
  RT-PCR
(0)
  HT-Seq
(0)
  Other
(4)
  All
(8,522)
 
  brain
(202)
  blood
(1,042)
  connective
(493)
  reproductive
(148)
  muscular
(79)
  digestive
(111)
  liver
(99)
  lung
(348)
  urinary
(172)
  endo/exo-crine
(360)
  embryo
(30)
  adult aerial structure
(3)
  young aerial structure
(9)
  root
(0)
  meristem/growing tissue
(0)
  flower/sexual organ
(60)
  seed/fruit/grain
(0)
  pooled
(45)
  unclassified
(721)
  all
(3,922)
 
Sample ID Title Number of Data Institute Submission date Platform Sample type Species Organ class Reasoning of the classification
Keywords used for the classification are shown with bold font.
1 GSM48122 Col_8mer1 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum
2 GSM48123 Col_8mer2 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum
3 GSM48124 Col_8mer3 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum
4 GSM48125 Col_CSC1 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum
5 GSM48126 Col_CSC2 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum Lot batch = 510690
6 GSM48127 Col_CSC3 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum Lot batch = 510690
7 GSM48128 Col_Mock1 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum Lot batch = 510690
8 GSM48129 Col_Mock2 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum Lot batch = 510690
9 GSM48130 Col_Mock3 22,810 University of Alabama 2005-04-12 [GeneChip] [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array (GPL198) RNA Arabidopsis thaliana
Arabidopsis thaliana
young aerial structure Growth Conditions and Treatments: Arabidopsis thaliana L. (Columbia-0) seeds were sterilized and grown hydroponically as previously described (Zhang et al., 2002, MPMI 15(9) 963-970). Briefly, Arabidopsis seeds were surface sterilized and allocated in 50 ml Falcon tubes containing 10 ml of liquid medium (1 X Murashige and Skoog Basal Salt Mixture + 2% Dextrose, pH 5.8). The tubes were incubated with gentle shaking in a growth chamber with the following settings: constant light at 125 µmol m-2 sec-1 at a temperature of 23 °C. After 14 days, the seedlings were treated with either hydrolyzed crab-shell chitin (Sigma-Aldrich, St. Louis, Missouri) at a final concentration of 100 µg/ml or the purified chito-tetramer (degree of polymerization, d.p. = 4) or octamer (d.p. =8) at a final concentration of 1 µM. The control seedlings were similarly treated with an equivalent amount of water. Whole seedlings were collected 30 minutes after treatment, immediately frozen in liquid N2, and stored at –80 °C for later use. Three independent replicates were conducted. RNA and Microarray Methods: Total RNA was extracted from the plants using a modified Trizol method (Chomczynski and Sashi, 1987) (see also Protocols Manual at the AFGC web page http://www.arabidopsis.org/info/2010_projects/comp_proj/AFGC/RevisedAFGC/AFGC_Protocols_Dec_2001L.pdf) and purified with a silica membrane column (Qiagen, RNeasy). Fifteen micrograms biotinylated complementary RNA (cRNA) was prepared and used to hybridize ATH1 Arabidopsis GeneChips (Affymetrix) using the Affymetrix manufacturer’s protocols. The array images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) 1.1 with the target intensity set to 500. These data were imported into GeneSpring 7.0 (Silicon Genetics, Redwood City, CA, USA). To remove chip-to-chip signal variation, each measurement was divided by the 50.0th percentile of all measurements in that sample. All samples were normalized to the reference data set, consisting of four replicates of Columbia-0, untreated. Each measurement for each gene was divided by the median of that gene’s intensity in the reference data set. The normalized values (Normalized Ratio) are reported along with the intensity values for this array. Keywords = chitin, defense, elicitor, mutant, powdery mildew, Erysiphe cichoracearum Lot batch = 510690