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Sample GSM846116 Query DataSets for GSM846116
Status Public on Jan 01, 2015
Title M4 cell, minus at 1h, biological rep3
Sample type RNA
 
Source name MCF10CA1a.cl1 (M4), vehicle treated, 1h
Organism Homo sapiens
Characteristics treatment: vehicle treated
time: 1h
cell line: MCF10Ca1a.cl1 (M4)
cell line origin: Breast epithelium
tumor stage represented: Malignant, high grade, metastatic
Treatment protocol Cells were grown to 50-60% confluence and then serum-starved in DMEM/F12 supplemented with Serum Replacement 1 for 16 hours prior to TGF-beta treatment with 5ng/ml or vehicle for 1 hour or 6 hour.
Growth protocol M1 and M2 cells were grown in DMEM/F12 medium supplemented with 10ug/ml, insulin, 20ng/ml EGF, 0.5ug/ml hydrocortisone, 100ng/ml cholera toxin and 5% horse serum. M3 and M4 cells were grown in DMEM/F12 medium supplemented with 5% Horse serum.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified by RNeasy Mini Kit (Qiagen) according to manufacturer's instructions. RNA quality was checked on Agilent Bioanalyzer. All samples used for microarray analysis have high quality score (RIN >9).
Label Biotin
Label protocol 100 ng of RNA was reverse transcribed and amplified using Ambion WT expression kit following manufacturer’s suggested protocol. Sense strand cDNA was fragmented and labeled using Affymetrix WT terminal labeling kit.
 
Hybridization protocol Three replicates of each group were hybridized to Affymetrix mouse (human) Gene ST 1.0 GeneChip in Affymetrix hybridization oven at 45C, 60rpm for 16 hrs. Wash and stain were performed on Affymetrix Fluidics Station 450
Scan protocol Genechips were scanned using an Affymetrix GeneChip Scanner 3000 and data was collected using Affymetrix AGCC software.
Description RNA extracted by RNeasy
Data processing Data were analyzed with Partek Genomics Suite (version 6.5) software using the RMA normalization algorithm with default format.
Original, Summarized, Difference, Filename, Chip Type, Attribute, cell, treatment, time, group, Scan Date, gene expression
 
Submission date Dec 08, 2011
Last update date Jan 01, 2015
Contact name Howard Yang
E-mail(s) [email protected]
Phone 2402765257
Organization name NCI
Street address 9609 Medical Center Dr.
City Rockville
State/province MD
ZIP/Postal code 20850
Country USA
 
Platform ID GPL6244
Series (2)
GSE34270 In vitro gene expression profile of TGFbeta-regulated genes in MCF10A-based xenograft model of breast cancer progression
GSE34277 MCF10A-based xenograft model of breast cancer

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
7892501 6.35786
7892502 4.64608
7892503 3.83427
7892504 8.18145
7892505 2.94913
7892506 3.71249
7892507 4.69841
7892508 5.15765
7892509 11.1419
7892510 3.60057
7892511 2.90547
7892512 6.69981
7892513 3.4433
7892514 10.7101
7892515 7.70597
7892516 5.57056
7892517 5.42385
7892518 2.93359
7892519 5.08549
7892520 7.96726

Total number of rows: 33297

Table truncated, full table size 516 Kbytes.




Supplementary file Size Download File type/resource
GSM846116_M4_minus_1h_3.CEL.gz 3.9 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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