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Sample GSM201991 Query DataSets for GSM201991
Status Public on Jun 18, 2007
Title Embryonic Reference, biological rep 3
Sample type RNA
 
Source name All living C. elegans sorted cells
Organism Caenorhabditis elegans
Characteristics cultured embryonic cells from wildtype (N2 isolate) nematodes
Growth protocol Gravid adults expressing unc-4::GFP (A-class) were subjected to bleach/NaOH treatment to release embryos. Embryos were harvested and then treated with chitinase to degrade the eggshell. Cells were dissociated and plated on poly-L-lysine coated dishes for 24 hrs to allow differentiation. Cells were removed from the culture dish and sorted using the FACStar Plus (Becton Dickinson, San Jose, CA) that had been flushed with egg buffer. ~90% enrichment of GFP+ cells was obtained. For Reference dataset, wildtype (N2) animals were subjected to the same dissociation/cell culture treatment. FACS isolated all non-propidium iodide stained (i.e. living) cells.
Extracted molecule total RNA
Extraction protocol RNA was isolated from sorted cells using the micro-RNA isolation kit (Stratagene) using the recommended volumes for 1 million cells.
Label biotin
Label protocol A 2-round IVT protocol (modified from the Affymetrix small-sample protocol) was used to convert 100 ng total RNA into biotinylated cRNA.
 
Hybridization protocol Following fragmentation, 10-15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip C. elegans Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
Description N2 #3
Gene expression data from all wildtype embryonic nematode cells
Data processing Data were normalized using Robust Multiarray analysis (RMA) in GeneTraffic (Stratagene). RMA normalized data were subjected to Significance Analysis of Microarray (SAM, Stanford) analysis. Enriched genes were obtained by finding genes with a 1.7x enriched at a False Discovery Rate (FDR) of less than or equal to 1%.
 
Submission date Jun 18, 2007
Last update date Aug 14, 2011
Contact name David Miller
E-mail(s) david.miller@vanderbilt.edu
Phone 6153433447
Fax 6159365673
URL http://exploration.vanderbilt.edu/news/news_worm.htm
Organization name Vanderbilt University
Department Cell and Developmental Biology
Street address 465 21st Avenue South
City Nashville
State/province TN
ZIP/Postal code 37232-8240
Country USA
 
Platform ID GPL200
Series (1)
GSE8159 A gene expression fingerprint of C. elegans embryonic motor neurons.

Data table header descriptions
ID_REF
VALUE Intensity values after RMA normalization

Data table
ID_REF VALUE
171720_x_at 115.3090947
171721_x_at 505.2771375
171722_x_at 572.355001
171723_x_at 105.773009
171724_x_at 98.86741255
171725_x_at 180.4699709
171726_x_at 162.2203099
171727_x_at 34.84631757
171728_x_at 62.95513654
171729_x_at 315.1125949
171730_x_at 29.57451066
171731_x_at 181.8682503
171732_x_at 163.6136563
171733_x_at 878.4653304
171734_x_at 1523.963949
171735_x_at 147.6160912
171736_x_at 345.309688
171737_x_at 2928.612168
171738_x_at 1099.398309
171739_x_at 49.13117093

Total number of rows: 22548

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM201991.CEL.gz 3.3 Mb (ftp)(http) CEL
GSM201991.EXP.gz 477 b (ftp)(http) EXP
Processed data included within Sample table

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