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Sample GSM201994 Query DataSets for GSM201994
Status Public on Jun 18, 2007
Title Embryonic A-class, biological rep 2
Sample type RNA
 
Source name unc-4::GFP positive cells (A-class)
Organism Caenorhabditis elegans
Characteristics cultured embryonic cells from unc-4::GFP transgenic animals
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 unc-4GFP#2
Gene expression data from embryonic A-class neurons
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 198.1161623
171721_x_at 298.0301373
171722_x_at 483.0821149
171723_x_at 131.0767526
171724_x_at 81.68773746
171725_x_at 147.7018055
171726_x_at 237.9840238
171727_x_at 27.24485522
171728_x_at 88.14346047
171729_x_at 230.4697386
171730_x_at 35.96410948
171731_x_at 211.7645725
171732_x_at 200.5742463
171733_x_at 210.9759196
171734_x_at 1815.755452
171735_x_at 150.8060126
171736_x_at 112.657096
171737_x_at 3112.807235
171738_x_at 1031.725513
171739_x_at 58.21932994

Total number of rows: 22548

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM201994.CEL.gz 3.0 Mb (ftp)(http) CEL
GSM201994.EXP.gz 476 b (ftp)(http) EXP
Processed data included within Sample table

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