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Sample GSM152877 Query DataSets for GSM152877
Status Public on Jan 16, 2007
Title Metastatic prostate tumor samples in retroperitoneal lymph node from patient FB561 FB561_2GU95Av2
Sample type RNA
 
Source name FB561_2G, metastatic prostate tumor samples in retroperitoneal lymph node from patient FB561
Organism Homo sapiens
Characteristics Tissue: prostate tumor metastases in retroperitoneal lymph node
Treatment protocol Specimens were received directly from the operating room. Samples (>500 mg) were excised and snap frozen in liquid nitrogen within 30 min of excision and stored at -80°C until extraction of RNA. Metastatic tumor samples were obtained from a warm autopsy program and processed similarly to primary tumors. An H&E stained frozen section of each sample was evaluated by a pathologist, to determine epithelial and stromal content and verify the presence of tumor in the sample. Dissection of the frozen tissue block was performed with the guidance of a marked H & E slide to minimize the presence of host tissue in the metastatic samples. All samples used in the study contained >80% tumor. Metastatic tumor samples were minced and divided into two equal portions to be extracted with the sample protocol used for each set of primary tumors.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with Qiagen Rneasy kit according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip HG-U95Av2 array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description Gene expression data from metastatic prostate cancer
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 200.
 
Submission date Dec 22, 2006
Last update date Mar 16, 2009
Contact name Federico Alberto Monzon
E-mail(s) [email protected]
Organization name The Methodist Hospital
Department Pathology
Lab Molecular Diagnostics
Street address 6565 Fannin St, MS205
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL8300
Series (2)
GSE6605 Expression data from Metastatic Prostate Tumor
GSE6919 Expression Data from Normal and Prostate Tumor Tissues

Data table header descriptions
ID_REF 12558
VALUE MAS5-calculated Signal intensity

Data table
ID_REF VALUE
100_g_at 369.9
1000_at 509.6
1001_at 103.6
1002_f_at 19.3
1003_s_at 35.8
1004_at 121.3
1005_at 274.5
1006_at 4.1
1007_s_at 332.1
1008_f_at 3120.9
1009_at 732
101_at 54.6
1010_at 22.5
1011_s_at 657.5
1012_at 10.4
1013_at 67.5
1014_at 309
1015_s_at 24.8
1016_s_at 50.7
1017_at 170.4

Total number of rows: 12558

Table truncated, full table size 176 Kbytes.




Supplementary file Size Download File type/resource
GSM152877.CEL.gz 2.6 Mb (ftp)(http) CEL

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