NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM742505 Query DataSets for GSM742505
Status Public on Jun 17, 2011
Title 103 wild-type untreated rep. 1
Sample type RNA
 
Channel 1
Source name WT/-RAM
Organism Bacillus subtilis
Characteristics strain: CU1065 wild-type
genotype/variation: wild-type
Extracted molecule total RNA
Extraction protocol Cells were grown to mid-log phase (OD600 0.4) and split into 2 flasks. One flask was treated with 5 µg/ml ramoplanin for 10 minutes. Total RNA was isolated using the RNeasy Mini Kit (Qiagen Sciences, Maryland) and treated with TURBO DNA-freeTM (Ambion). RNA concentrations were quantified and cDNA was synthesized from 10 µg total RNA and differentially labeled according to manufacturer’s instructions with Cy3 (combined reference RNA) and Cy5 (sample) (Amersham). Before and after labeling for 1 h at room temperature) cDNA was purified using the Qiagen MinElute PCR Purification Kit (Qiagen, Maryland).
Label Cy5
Label protocol cDNA synthesis was performed using the SuperScriptTM Plus (Invitrogen) as per the manufacturer’s instructions using 10 microgram of total RNA. Total cDNA was labeled for 1h Cy3/5 Dyes to amino-allyl cDNA.
 
Channel 2
Source name WT+/-RAM, liaR +/-RAM (pooled reference RNA)
Organism Bacillus subtilis
Characteristics strain: CU1065
genotype/variation: wild-type, liaR deletion (pooled)
Extracted molecule total RNA
Extraction protocol Cells were grown to mid-log phase (OD600 0.4) and split into 2 flasks. One flask was treated with 5 µg/ml ramoplanin for 10 minutes. Total RNA was isolated using the RNeasy Mini Kit (Qiagen Sciences, Maryland) and treated with TURBO DNA-freeTM (Ambion). RNA concentrations were quantified and cDNA was synthesized from 10 µg total RNA and differentially labeled according to manufacturer’s instructions with Cy3 (combined reference RNA) and Cy5 (sample) (Amersham). Before and after labeling for 1 h at room temperature) cDNA was purified using the Qiagen MinElute PCR Purification Kit (Qiagen, Maryland).
Label Cy3
Label protocol cDNA synthesis was performed using the SuperScriptTM Plus (Invitrogen) as per the manufacturer’s instructions using 10 microgram of total RNA. Total cDNA was labeled for 1h Cy3/5 Dyes to amino-allyl cDNA.
 
 
Hybridization protocol Labeled cDNA samples were combined plus hybridization buffer (2X = 50% formamide, 10X SSC, 0.1% SDS). cDNA mix was denatured at 100oC and hybridized overnight at 42oC to DNA microarray slides (oligos from Sigma Genosys #BACLIB96; ultraGAPS coated slides Corning #40016) which had been prehybridized for at least 45 min at 42oC in 1% bovine serum albumin, 5X SSC (1X SSC is 0.15 M NaCl and 0.015 M sodium citrate), 0.1% sodium dodecyl sulfate (SDS), washed in water and dried. Following hybridization the slides were washed sequentially in: 1X SSC + 0.2% SDS for 4 min at 42oC, 0.1X SSC + 0.2% SDS for 4 min at room temperature, 0.1X SSC for 4 min at room temperature, 0.1X SSC for 4 min at room temperature, and spun until dry.
Scan protocol Arrays were scanned using a GenePixTM 4000B array scanner (Axon Instruments, Inc.)
Raw data files were produced from the scanned images using the GenePix Pro 3.0 software package (GPR files).
Data processing Red/green fluorescence intensity values were normalized using the GenePix Pro 3.0 software package such that the ratio of medians of all features was equal to 1. Fold changes equal to average of ramoplanin treated/untreated samples (635) / average of combined reference RNA (532). Ave represents the average of medians for duplicate spots (minus median of background).
 
Submission date Jun 15, 2011
Last update date Jun 17, 2011
Contact name John D. Helmann
E-mail(s) [email protected]
Phone 607 255 6570
Organization name Cornell University
Department Microbiology
Street address 372 Wing Hall
City Ithaca
State/province NY
ZIP/Postal code 14853
Country USA
 
Platform ID GPL13726
Series (2)
GSE30002 Bacillus subtilis CU1065 ramoplanin stimulon
GSE30003 The GntR family repressor YtrA responds to cell wall antibiotics

Data table header descriptions
ID_REF
VALUE log2 of PRE_VALUE
PRE_VALUE Fold change representing test sample/reference sample

Data table
ID_REF VALUE PRE_VALUE
581 0.1775 1.130952381
3032 0.5214 1.435309973
3535 -0.0314 0.978494624
4176 -0.0201 0.986145069
2479 0.6007 1.516483516
3120 0.1616 1.118518519
3391 0.1468 1.107142857
2335 0
1279 0.1520 1.111111111
223 0.2224 1.166666667
3395 0.0000 1
1423 -0.0143 0.990106007
367 0.8489 1.801065719
3539 0.7936 1.733400402
2483 0.8063 1.748759305
1427 0.8525 1.805589307
2064 0.3187 1.247191011
2339 0.1999 1.148599945
3217 0.7655 1.7
1283 -0.3219 0.8

Total number of rows: 4109

Table truncated, full table size 90 Kbytes.




Supplementary file Size Download File type/resource
GSM742505_103_W1-_110603.gpr.gz 269.2 Kb (ftp)(http) GPR
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap