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Sample GSM129327 Query DataSets for GSM129327
Status Public on Mar 31, 2009
Title E_C_Gad_sample3
Sample type RNA
 
Source name embryo culture 5-7 days, 2.1 kb Gad1(s)-RFP
Organism Drosophila melanogaster
Characteristics Strain: 2.1 kb Gad1(s)-RFP
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, 2.1 kb Gad1(s)-RFP
E_C_Gad_sample3 (H+)
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 9.44132888
1622892_s_at 9.426257909
1622893_at 10.82142627
1622894_at 5.276525936
1622895_at 8.785452811
1622896_at 7.057278578
1622897_at 5.810905126
1622898_a_at 8.799415551
1622899_at 4.250882764
1622900_at 3.624917277
1622901_at 7.842688679
1622902_at 9.726039775
1622903_s_at 8.71007643
1622904_at 4.743612249
1622905_at 3.565228383
1622906_at 7.531873428
1622907_at 7.287482589
1622908_a_at 8.965242319
1622909_at 10.68503114
1622910_at 3.774683755

Total number of rows: 18952

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM129327.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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