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Sample GSM210110 Query DataSets for GSM210110
Status Public on Jul 13, 2007
Title 0 hr muscle, biological rep 1
Sample type RNA
 
Source name myo-3::GFP positive sorted cells from freshly dissociated embryos
Organism Caenorhabditis elegans
Characteristics embryonic cells from myo-3::GFP transgenic animals
Growth protocol Gravid adults expressing myo-3::GFP 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 either sorted immediately (0hr dataset) or plated on poly-L-lysine coated dishes for 24 hrs to allow differentiation and then removed from the culture dish and sorted (24 hr dataset). Cells were 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 Caenorhabditis 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 Gene expression data from freshly dissociated embryonic muscle 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 1.8% (0hr) or less than or equal to 1.2% (24hr)..
 
Submission date Jul 12, 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)
GSE8462 The embryonic muscle transcriptome of Caenorhabditis elegans

Data table header descriptions
ID_REF
VALUE RMA

Data table
ID_REF VALUE
171720_x_at 89.30807611
171721_x_at 621.9098573
171722_x_at 270.0636678
171723_x_at 80.50008532
171724_x_at 69.92590906
171725_x_at 83.25626223
171726_x_at 175.2671158
171727_x_at 25.16767194
171728_x_at 347.9031735
171729_x_at 178.9757138
171730_x_at 22.20900609
171731_x_at 165.948521
171732_x_at 107.2373069
171733_x_at 96.81468345
171734_x_at 3368.371607
171735_x_at 95.0139398
171736_x_at 163.2677719
171737_x_at 2400.185361
171738_x_at 1779.430642
171739_x_at 1739.466418

Total number of rows: 22548

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM210110.CEL.gz 3.1 Mb (ftp)(http) CEL
GSM210110.EXP.gz 491 b (ftp)(http) EXP
Processed data included within Sample table

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