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Sample GSM201992 Query DataSets for GSM201992
Status Public on Jun 18, 2007
Title Embryonic Reference, biological rep 4
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 #4
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 155.4064233
171721_x_at 664.3784391
171722_x_at 299.9116469
171723_x_at 137.2753215
171724_x_at 118.7122942
171725_x_at 151.2905747
171726_x_at 314.5964312
171727_x_at 34.0152094
171728_x_at 94.99038455
171729_x_at 315.1125949
171730_x_at 20.56730331
171731_x_at 313.0125949
171732_x_at 183.9994513
171733_x_at 718.2830959
171734_x_at 671.2191756
171735_x_at 99.93303509
171736_x_at 361.9362093
171737_x_at 3202.821406
171738_x_at 944.7721704
171739_x_at 56.30226546

Total number of rows: 22548

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM201992.CEL.gz 3.4 Mb (ftp)(http) CEL
GSM201992.EXP.gz 476 b (ftp)(http) EXP
Processed data included within Sample table

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