NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM605024 Query DataSets for GSM605024
Status Public on Nov 22, 2011
Title 465 tumor TILN
Sample type RNA
 
Source name tumor TILN
Organism Homo sapiens
Characteristics patient code: 465
disease: melanoma
tissue: tumor-infiltrated lymph node (TILN)
cell type: CD8+ T cells
tcr specificity (or naive): self/tumor (Melan-A/MART-1 26-35 A27L)
age: 48 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 tumor-infiltrated lymph node.
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 6.766
A_32_P77178 9.708
A_23_P212522 5.968
A_24_P934473 5.9
A_24_P9671 12.055
A_32_P29551 6.692
A_24_P801451 10.479
A_32_P30710 15.483
A_32_P89523 9.727
A_24_P704878 11.741
A_32_P86028 13.716
A_24_P470079 10.875
A_23_P65830 8.835
A_24_P595567 6.513
A_24_P391591 11.011
A_24_P799245 6.524
A_24_P835500 6.396
A_23_P54340 7.315
A_23_P67555 5.815
A_24_P286412 11.542

Total number of rows: 38660

Table truncated, full table size 708 Kbytes.




Supplementary file Size Download File type/resource
GSM605024.txt.gz 9.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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