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Sample GSM3084292 Query DataSets for GSM3084292
Status Public on Apr 07, 2018
Title Sinorhizobium meliloti EC220, biological rep1
Sample type RNA
 
Source name Rm1021, merodiploid with ChvI D52E mutation/wild type ChvI and hygromycin resistance marker
Organism Sinorhizobium meliloti
Characteristics strain: EC220
Treatment protocol Stop solution (5% buffer equilibrated phenol in ethanol) was added to bacterial cultures, at one tenth the culture volume, before centrifugation at 4 degrees celsius. Bacterial cell pellets were frozen in liquid nitrogen and stored at -80 degrees celsius until RNA extraction.
Growth protocol Bacteria were cultured in LB medium supplemented with 500 ug/ml streptomycin. Cells were harvested at OD-600 = 0.5 - 0.7
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using a Qiagen RNeasy kit with modifications as described by Barnett et al. 2004 Proc Natl Acad Sci USA volume 101 pages 16636 to 16641.
Label biotin
Label protocol cDNA was fragmented and biotinylated as described by Barnett et al. 2004.
 
Hybridization protocol Four micrograms of biotinylated cDNA was hybridized to each chip at 48 degrees celsius for 16 hours as described by Barnett et al. 2004. GeneChips were washed and stained in the Affymetrix Fluidics Station 400
Scan protocol Chips were scanned at the Stanford PAN facility using an Affymetrix scanner 3000 7G
Data processing The data were analyzed using Affymetrix software GCOS v1.4 with Affymetrix default analysis setting and global scaling as the normalization method. The mean target intensity of each array was arbitrarily set to 500. Affymetrix Data Mining Tool v3.1 was used for data mining as previously described by Barnett et al. 2004.
 
Submission date Apr 06, 2018
Last update date Apr 07, 2018
Contact name Melanie J Barnett
Organization name Stanford University
Department Biology
Lab Sharon R. Long
Street address 371 Jane Stanford Way
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platform ID GPL9757
Series (1)
GSE112819 Identification of direct transcriptional target genes of ExoS/ChvI two-component signaling in Sinorhizobium meliloti

Data table header descriptions
ID_REF
VALUE GCOS v1.4 signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
i14523056f1_x_at 20.6 A 0.919434
ci14523056f1_x_at 65.7 A 0.466064
i14523056f2_x_at 21.9 A 0.780518
ci14523056f2_x_at 7.8 A 0.976074
i14523056f3_x_at 18.9 A 0.893555
ci14523056f3_x_at 120.1 A 0.088379
i14523056f4_x_at 295.1 P 0.000244
ci14523056f4_x_at 72.1 A 0.398926
i14524469f1_x_at 55.1 A 0.558105
ci14524469f1_x_at 263 P 0.00293
i14524469f2_x_at 156.1 A 0.19458
ci14524469f2_x_at 48.6 A 0.27417
i15141458f1_x_at 36.5 A 0.5
ci15141458f1_x_at 1318.3 P 0.011719
i15141458f2_x_at 18.2 A 0.625
ci15141458f2_x_at 60.2 A 0.5
i15963754f1_x_at 10.5 A 0.5625
ci15963754f1_x_at 134.5 A 0.316406
i15963754f2_x_at 591.9 P 0.005859
ci15963754f2_x_at 120.8 A 0.111328

Total number of rows: 12080

Table truncated, full table size 420 Kbytes.




Supplementary file Size Download File type/resource
GSM3084292_EC220_LB_1.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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