NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2717824 Query DataSets for GSM2717824
Status Public on Jul 27, 2017
Title Adult 90%D 1SY/2.5SY F2
Sample type RNA
 
Source name Adult female collected at 90% cohort mortality, raised on the 1SY diet as a larvae and maintained on the 2.5SY diet as an adult
Organism Drosophila melanogaster
Characteristics Sex: female
age: 90% cohort mortality
larval diet: 1SY
adult diet: 2.5SY
tissue: whole body
Treatment protocol Adults in each age-class were flash frozen in liquid nitrogen and transferred to the -80 to await RNA extraction.
Growth protocol Flies were raised on one of three diets as larvae (0.25SY, 1SY, or 2.5SY) These three diets differed only in the amount of sugar and yeast they contained. The 1SY diet was identical to the standard laboratory diet (70g yeast, 100g sugar, 20g agar, 15mL nipagine, and 3mL propionic acid per liter of water), while the 0.25SY and 2.5SY diets contained 25% and 250% as much sugar and yeast as the 1SY diet, respectively. Newly eclosed adults were split across these same three diets in a fully factorial design and maintained on their adult diet until their death. Samples were collected at 1 day post eclosion and at 10% and 90% cohort mortality.
Extracted molecule total RNA
Extraction protocol RNA extraction was performed using the Machery Nagel Nucleospin II kit (Machery and Nagel) following the manufacturers instructions. We extracted RNA from whole bodies of five flies per replicate, with four replicates per combination of sex, larval diet, adult diet and age (4 replicates x 2 sexes x 3 larval diets x 3 adult diets x 3 ages = 216 arrays)
Label biotin
Label protocol Biotinylated cRNA were prepared using the Affymetrix 3' IVT-Express Labeling Kit (#901229) according to the standard Affymetrix protocol from 100 ug total RNA per sample.
 
Hybridization protocol Following fragmentation, 15 ug of cRNA were hybridized to the Affymetrix Drosophila 2.0 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix 3000G scanner.
Description 7032-07-243
Data processing The data was processed using the robust multi-array average (RMA) algorithm to perform background adjustment, quantile normalization and summarization
 
Submission date Jul 26, 2017
Last update date Jan 23, 2018
Contact name Christina May
E-mail(s) [email protected]
Organization name Wageningen University
Street address Droevendaalsesteeg 1
City Wageningen
State/province Gelderland
ZIP/Postal code 6708 PB
Country Netherlands
 
Platform ID GPL1322
Series (1)
GSE101882 Gene expression of young, middle-aged and old Drosophila melanogaster exposed to different levels of larval and adult diet

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1616608_a_at 13.18911733
1622892_s_at 9.855977699
1622893_at 13.4582099
1622894_at 9.145680292
1622895_at 10.04435788
1622896_at 8.935502743
1622897_at 5.55468034
1622898_a_at 10.80698183
1622899_at 5.264157001
1622900_at 4.042851053
1622901_at 6.227892756
1622902_at 7.55339111
1622903_s_at 10.00637783
1622904_at 5.971391718
1622905_at 4.042266725
1622906_at 7.975589921
1622907_at 9.678067457
1622908_a_at 8.556699339
1622909_at 11.56447589
1622910_at 4.282496777

Total number of rows: 18952

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM2717824_7032-07-243.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap