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Sample GSM140886 Query DataSets for GSM140886
Status Public on Nov 20, 2006
Title C. novyi-NT Mid Log Replicate 3
Sample type RNA
 
Source name C. novyi-NT in Mid Log Phase
Organism Clostridium novyi NT
Characteristics C. novyi-NT in Mid Log Phase
Growth protocol Overnight cultures were diluted into fresh deoxygenated culture medium and anaerobic incubation continued until bacteria entered mid (OD600 = 0.6) log phase.
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 218.354533
NT0100P0000000218 126.798089
NT0100P0000000319 16.833083
NT0100P0000000530 102.560781
NT0100P0000000693 64.658558
NT0100P0000001071 366.824795
NT0100P0000001435 482.824562
NT0100P0000001713 502.407895
NT0100P0000001864 340.241803
NT0100P0000002024 31.30402
NT0100P0000002085 530.407894
NT0100P0000002149 34.602438
NT0100P0000002220 289.994323
NT0100P0000002289 141.222759
NT0100P0000002361 243.171937
NT0100P0000002519 29.334699
NT0100P0000002579 55.579308
NT0100P0000002643 440.491239
NT0100P0000002741 45.259576
NT0100P0000002872 13.776071

Total number of rows: 11630

Table truncated, full table size 331 Kbytes.




Supplementary file Size Download File type/resource
GSM140886.gpr.gz 172.4 Kb (ftp)(http) GPR

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