NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM402200 Query DataSets for GSM402200
Status Public on May 12, 2010
Title HMEC 184D11pM85X Intermediate
Sample type RNA
 
Source name HMEC
Organism Homo sapiens
Characteristics cell type: mammary epithelial cell
individual: 184
passage: 11p
growth status: Intermediate-Prestasis
Treatment protocol Cell cultures grown in the indicated media were harvested and different points in their growth from early passage good growing to near stasis, agonescence, or senescence.
Growth protocol Finite life span HMEC and HMFC from Specimens 184, 48 and 240L were obtained from reduction mammoplasty tissue of women aged 21, 16, and 19 respectively. HMEC were grown starting from organoids in either serum free MCDB170 medium, or the serum-containing M85+CT±X medium described in this publication. HMFC were grown in DME/F12+FCS+I
Extracted molecule total RNA
Extraction protocol Cell were lysed with trizol reagent (Invitrogen) according manufacturer's protocol. RNA was resuspended in 100 µl nuclease free water and subject to a second step purification on ion exchange column (Qiagen)
Label Biotin
Label protocol For each sample, the RNA target is prepared by annealing 2.0µg of total RNA in 5µl water with 5µl of 10µM T7 (Oligo dt) primer. First and second strand cDNA synthesis is performed and the cDNA products purified using magnetic beads. Labeled cRNA is synthesized from the cDNA using T7 RNA polymerase followed by clean-up with magnetic beads. Purified cRNA is quantitated and fragmented.
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip HT_HG-U133A Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Human Cell Lines
Data processing Raw probe level intensities were processed for background correction, normalization and summarization using Probel level linear (PLM) model in LIMMA module(v.2.16.3) of Bioconductor package.
 
Submission date May 12, 2009
Last update date May 12, 2009
Contact name Sanchita Bhattacharya
E-mail(s) SBhattacharya@lbl.gov
Phone 510-486-6881
Organization name MIT
Street address 1 Cyclotron Rd
City Berkely
State/province CA
ZIP/Postal code 94720
Country USA
 
Platform ID GPL3921
Series (1)
GSE16058 Distinctions between the stasis and telomere attrition senescence barriers in cultured human mammary epithelial cells

Data table header descriptions
ID_REF
VALUE Log2 PLM value

Data table
ID_REF VALUE
1007_s_at 11.15560581
1053_at 7.814590429
117_at 5.271657544
121_at 8.332681231
1255_g_at 5.107559961
1294_at 5.953036906
1316_at 5.647281768
1320_at 5.246228667
1405_i_at 4.829075784
1431_at 4.863162137
1438_at 5.865665715
1487_at 7.590009816
1494_f_at 5.958690606
1598_g_at 9.650705408
160020_at 8.784466284
1729_at 8.01520301
177_at 6.605961172
1773_at 6.528005122
179_at 7.313679366
1861_at 7.877889635

Total number of rows: 22277

Table truncated, full table size 496 Kbytes.




Supplementary file Size Download File type/resource
GSM402200.CEL.gz 2.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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