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Sample GSM4712754 Query DataSets for GSM4712754
Status Public on May 10, 2023
Title 160108_3200: Sinorhizobium meliloti JOE3200, biological rep2
Sample type RNA
 
Source name Rm1021 strain carrying the empty vector, pCM130 (control strain)
Organism Sinorhizobium meliloti
Characteristics strain: JOE3200
genotype/variation: carrying the empty vector, pCM130 (control strain)
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 grown overnight in PYE medium with 0.5 ug ml-1 oxytetracycline; diluted to ~0.25 to ~0.30 OD-600 in 25 ml of the same medium with 10 mM taurine, in 125-ml flasks; and allowed to grow for 4.5 hours, shaken (250 rpm) at 30°C, 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, prior to 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 Aug 06, 2020
Last update date May 12, 2023
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)
GSE155833 Identifying the regulon of the Sinorhizobium meliloti JspA protease

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
n14523056_at 9.06329
n14523057_at 8.69151
n14523058_at 7.73609
n14523059_at 8.13901
n14523060_at 7.76887
n14523061_at 8.04648
n14523062_at 7.08675
14523062i14523064f1_x_at 9.0515
c14523062i14523064f1_x_at 6.78112
n14523064_at 8.98549
14523064i14523065f1_x_at 7.7836
c14523064i14523065f1_x_at 6.57543
14523064i14523065f2_x_at 5.3286
c14523064i14523065f2_x_at 5.45918
n14523065_s_at 11.1088
n14523066_s_at 9.24111
14523066i14523067f1_x_at 6.00507
c14523066i14523067f1_x_at 6.45017
14523066i14523067f2_x_at 7.73172
c14523066i14523067f2_x_at 5.7889

Total number of rows: 12080

Table truncated, full table size 316 Kbytes.




Supplementary file Size Download File type/resource
GSM4712754_160108_3200.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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