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Sample GSM605031 Query DataSets for GSM605031
Status Public on Nov 22, 2011
Title 1013 tumor PBMC, repl 2
Sample type RNA
 
Source name tumor PBMC
Organism Homo sapiens
Characteristics patient code: 1013
disease: melanoma
tissue: peripheral blood
cell type: CD8+ T cells
tcr specificity (or naive): self/tumor (Melan-A/MART-1 26-35 A27L)
age: 59 years
Sex: male
Treatment protocol Mononuclear cells were purified by density gradient using Lymphoprep and immediately frozen. CD8+ T cells were enriched using magnetic bead sorting. Cells were stained on ice and then diluted at one million cells/ml for optimal sorting speed and high purity.
Growth protocol Samples were processed ex vivo.
Extracted molecule total RNA
Extraction protocol Using a Vantage SE, 1000 cells from each cell population were sorted directly into lysis and storage buffer, as provided by Miltenyi Biotec. After sorting, the lysed cells were incubated for 10min at 45°C and then directly frozen at –80°C.
Label Cy3
Label protocol 250 ng of each of the cDNAs were used as template for Cy3 labeling, which was performed according to Miltenyi Biotec’s undisclosed protocol.
 
Hybridization protocol The Cy3-labeled cDNAs were hybridized overnight (17 hours, 65°C) to an Agilent Whole Human Genome Oligo Microarray 4 x 44K using Agilent’s recommended hybridization chamber and oven. Microarrays were washed once with 6x SSPE buffer containing 0.005% N- lauroylsarcosine for 1 min at room temperature followed by a second wash with pre-heated 0.06x SSPE buffer (37 °C) containing 0.005% N-lauroylsarcosine for 1 min. The last washing step was performed with acetonitrile for 30 sec.
Scan protocol Fluorescence signals of the hybridized Agilent Microarrays were detected using Agilent’s Microarray Scanner System (Agilent Technologies).
Description Set 2
Gene expression ex vivo of tumor-specific T cells from blood.
Data processing Raw intensities from the Feature Extraction files were used and analyzed using R and Bioconductor applying the Agi4x44PreProcess package.
 
Submission date Oct 05, 2010
Last update date Nov 22, 2011
Contact name Lukas Baitsch
E-mail(s) [email protected]
Organization name Dana Farber Cancer Institute
Department Cancer Biology
Lab Jean Zhao
Street address 450 Brookline Avenue
City Boston
State/province MA
ZIP/Postal code 02215
Country USA
 
Platform ID GPL6480
Series (1)
GSE24536 Molecular signature of CD8+ T cell exhaustion in metastases but not in peripheral blood from melanoma patients

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_24_P66027 7.328
A_32_P77178 9.843
A_23_P212522 9.446
A_24_P934473 5.973
A_24_P9671 12.497
A_32_P29551 6.998
A_24_P801451 8.856
A_32_P30710 15.533
A_32_P89523 12.361
A_24_P704878 12.1
A_32_P86028 13.939
A_24_P470079 9.282
A_23_P65830 8.33
A_24_P595567 6.855
A_24_P391591 11.537
A_24_P799245 5.875
A_24_P835500 6.967
A_23_P54340 7.138
A_23_P67555 6.055
A_24_P286412 6.973

Total number of rows: 38660

Table truncated, full table size 708 Kbytes.




Supplementary file Size Download File type/resource
GSM605031.txt.gz 9.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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