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Sample GSM129324 Query DataSets for GSM129324
Status Public on Mar 31, 2009
Title E_C_Cha_sample5
Sample type RNA
 
Source name embryo culture 5-7 days, 7.4 kb Cha-Gal:UAS-GFP
Organism Drosophila melanogaster
Characteristics Strain: 7.4 kb Cha-Gal:UAS-GFP
Age: Adults for collection were 2 weeks old
Tissue: Embryo culture
Treatment protocol Embryo collection and culture were performed as previously described (Salvaterra, P.M., Hayashi, I., Perez-Magallanes, M., & Ikeda, K. (2006) Primary culture of Drosophila embryo cells. in: Cell and Tissue Culture: Assorted Techniques, Elsevier Science USA, pp. 151-155). Cultures were initiated by dissociating early gastrula stage embryos prior to the differentiation of any neurons.
Growth protocol Cultures were incubated at 25 C for 5-8 days prior to dissociation and harvesting for Fluorescent Active Cell Sorting (FACS). After this time the cells were fully differentiated into a variety of neuronal. We plated approximately 7.0 x 10E7 cells.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from FACS sorted fractions using the RNA-STAT 60 kit (Iso Tex Diagnostic, Friendswood TX, USA). The RNA yield was measured by the absorbance at 260 nm and a rough estimate of RNA quality was obtained from the A260/280 ratio. Samples were treated with DNAse I (Ambion, Austin TX, USA) to remove contaminating. RNA clean of any contaminants was monitored by microcapillary electrophoresis (Bioanalyzer 2100, Agilent Technologies, Palo Alto, CA, USA).
Label biotin
Label protocol Standard Affymetrix protocol.
 
Hybridization protocol Standard Affymetrix protocol.
Scan protocol Standard Affymetrix protocol.
Description embryo culture 5-7 days, 7.4 kb Cha-Gal:UAS-GFP
E_C_Cha_sample5 (P+)
Data processing The data presented here have been processed using the R-Project Bioconductor statistical tools package using the affy library. The following were applied: RMA background correction, pmonly probe-level correction, quantile normalization, median-polish summary method. Raw data is provided in the form of .CEL files.
 
Submission date Aug 18, 2006
Last update date Aug 28, 2018
Contact name Paul M. Salvaterra
E-mail(s) [email protected]
Phone (626) 301-8364
Fax (626) 301-8908
Organization name Beckman Research Institute. City of Hope National Medical Center
Department Neuroscience
Street address 1500 E. Duarte Rd
City Duarte
State/province CA
ZIP/Postal code 91010
Country USA
 
Platform ID GPL1322
Series (1)
GSE10773 Expression profiling of transgenic Drosophila: neurons
Relations
Reanalyzed by GSE119084

Data table header descriptions
ID_REF
VALUE RMA-processed signal intensity

Data table
ID_REF VALUE
1616608_a_at 8.449102196
1622892_s_at 9.78737444
1622893_at 6.359417759
1622894_at 5.675927189
1622895_at 9.608406744
1622896_at 6.564830264
1622897_at 5.389843398
1622898_a_at 9.65922218
1622899_at 4.324560169
1622900_at 3.730575584
1622901_at 6.602143943
1622902_at 9.608441043
1622903_s_at 9.063938917
1622904_at 4.503050346
1622905_at 3.417406827
1622906_at 6.352495482
1622907_at 7.529113428
1622908_a_at 9.454643948
1622909_at 10.99541144
1622910_at 3.767759411

Total number of rows: 18952

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM129324.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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