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Sample GSM3560476 Query DataSets for GSM3560476
Status Public on Aug 01, 2019
Title Sinorhizobium meliloti RFF231 pSRKGm, biological rep3
Sample type RNA
 
Source name rpoH1rpoH2 deletion strain RFF231 pSRKGm (control strain, carrying empty vector)
Organism Sinorhizobium meliloti
Characteristics genotype/variation: rpoH1rpoH2 deletion
strain: RFF231 pSRKGm
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 Starter cultures were diluted to ~0.1 OD-600 in 20 ml M9 sucrose medium with 50 ug ml-1 Gm and 500 ug ml-1 Sm, in 250 ml baffled flasks, and allowed to grow to mid-exponential phase (~0.5 to ~0.7 OD-600), with replicates from a single experiment grown to within ~0.1 OD-600 units of each other, and shaking (250 rpm) at 30°C. At mid-exponential phase, IPTG was added to a final concentration of 0.5 mM and the cells were grown for one hour before harvest.
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 Partek Genomics Suite 6.6 software, with the following settings: RMA for background correction; quantile normalization; log base 2 transformation; median polish summarization
 
Submission date Jan 11, 2019
Last update date Aug 01, 2019
Contact name Melanie J Barnett
E-mail(s) melbar@stanford.edu
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 (2)
GSE124982 Sinorhizobium meliloti as a model system to study Ca. Liberibacter asiaticus regulators. [RpoH]
GSE124984 Sinorhizobium meliloti as a model system to study Ca. Liberibacter asiaticus regulators.

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
c15967040_at 7.88101
c15967066_at 8.53723
c15965467i15965468f1_x_at 5.97644
15965467i15965468f1_x_at 6.1663
n15965467_at 7.41541
c15965206_at 8.49011
crna61i15965886f1_x_at 6.43122
rna61i15965886f1_x_at 10.922
rna61_at 10.0819
n15963831_at 9.3419
c15966619_at 8.78865
c15966492_at 9.99562
n15966596_at 10.9652
c15966488_at 10.9851
c15966380i15966381f1_x_at 7.84056
15966380i15966381f1_x_at 10.2221
n15966380_at 10.6786
c15966155i15966156f2_x_at 8.75273
15966155i15966156f2_x_at 13.005
c15966155i15966156f1_x_at 8.21405

Total number of rows: 12080

Table truncated, full table size 316 Kbytes.




Supplementary file Size Download File type/resource
GSM3560476_3D_RFF231_pSRKGm.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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