NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM140814 Query DataSets for GSM140814
Status Public on Nov 20, 2006
Title C. novyi-NT Early Log Replicate 1
Sample type RNA
 
Source name C. novyi-NT in Early Log Phase
Organism Clostridium novyi NT
Characteristics C. novyi-NT in Early Log Phase
Growth protocol Overnight cultures were diluted into fresh deoxygenated culture medium and anaerobic incubation continued until bacteria entered early (OD600 = 0.2) log phases.
Extracted molecule total RNA
Extraction protocol Vegetative bacteria or spores were collected by centrifugation and homogenized by vortexing in RNAwiz buffer (RiboPureTM-Bacteria kit, Ambion, Austin, TX) containing 250 µL of Zirconia beads (Biospec, Bartlesville, OK) for 10 minutes at 4°C, followed by a 5-min break. This cycle was repeated 12 times to ensure disruption of the spores (as assessed by phase contrast microscopy and RNA yield). RNA was purified with the RiboPureTM-Bacteria kit (Ambion) following the manufacturer’s instructions.
Label biotin
Label protocol total RNA was reverse transcribed with SuperScript II Reverse Transcriptase (Invitrogen). The first-strand cDNA was fragmented by DNase I (Promega, Madison WI) and labeled with biotinylated ddATP through a terminal transferase end-labeling reaction.
 
Hybridization protocol Hybridization with the end-labeled samples was carried out at 45°C for 16 hours in 100 mM MES, 1 M NaCl, 20 mM EDTA, 0.01% Tween 20 and 10.5% glycerol.
Scan protocol After washing, the arrays were stained with Cy3-Streptavidin, followed by scanning with an Axon 4000B scanner.
Description The features were extracted by using the NimbleScan software.
Data processing Data was analyzed with the Bioconductor project using quantile normalization (see:Bolstad B, Irizarry R, Astrand M, Speed T (2003) A comparison of normalization methods for high density oligonucleotide array data based on bias and variance. Bioinformatics 19 (2), p185-193) and gene calls generated using the RMA algorithm (Robust multichip average described in Biostatistics 2003 Apr;4(2):249-64 ).
 
Submission date Oct 18, 2006
Last update date Nov 20, 2006
Contact name Xin Huang
E-mail(s) xhuang8@jhmi.edu
Organization name Johns Hopkins University
Department Oncology
Street address 1650 Orleans Street, CRB I, Room 520
City Baltimore
State/province MD
ZIP/Postal code 21231
Country USA
 
Platform ID GPL4463
Series (1)
GSE6087 Transcriptomes of Clostridium novyi-NT

Data table header descriptions
ID_REF
VALUE Normalized expression value

Data table
ID_REF VALUE
NT0100P0000000101 245.80708
NT0100P0000000218 217.93338
NT0100P0000000319 37.426
NT0100P0000000530 305.55757
NT0100P0000000693 101.10692
NT0100P0000001071 136.35104
NT0100P0000001435 328.44186
NT0100P0000001713 767.87622
NT0100P0000001864 248.58475
NT0100P0000002024 36.89007
NT0100P0000002085 467.16624
NT0100P0000002149 244.97467
NT0100P0000002220 237.51664
NT0100P0000002289 157.3822
NT0100P0000002361 266.3591
NT0100P0000002519 102.75562
NT0100P0000002579 102.75562
NT0100P0000002643 659.95765
NT0100P0000002741 97.5366
NT0100P0000002872 75.85584

Total number of rows: 11630

Table truncated, full table size 320 Kbytes.




Supplementary file Size Download File type/resource
GSM140814.gpr.gz 171.9 Kb (ftp)(http) GPR

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