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Sample GSM5082008 Query DataSets for GSM5082008
Status Public on Feb 15, 2021
Title Non-cancerous Renal Tissue 134
Sample type genomic
 
Channel 1
Source name Non-cancerous renal tissue, donor R134
Organism Homo sapiens
Characteristics subject id: donor R134
gender: Female
age: 64
tissue type: Non-cancerous renal tissue
molecule subtype: Anti-5-mC monoclonal antibody 33D3 immunoprecipitated DNA
Treatment protocol Tissue samples were obtained from partial or radical nephrectomy material of patients diagnosed with clear cell renal cell carcinoma. None of the patients had preoperatively received radiotherapy, chemotherapy, or hormone therapy.
Extracted molecule genomic DNA
Extraction protocol Renal tissue samples were homogenized using liquid nitrogen and cryoPREP™ CP02 Impactor with tissue TUBE TT1 (Covaris, Woburg, MA, USA). Homogenized tissue powder were treated for up to 18 h at 55 °C with 10-25 μl of proteinase K and 500 μl of lysis buffer, consisting of 50 mM Tris-HCl pH 8.5, 1 mM EDTA, 0.5% Tween-20. DNA was extracted following the standard phenol-chloroform purification and ethanol precipitation protocol.
Label Cy5
Label protocol Cyanine-5 and Cyanine-3 labeled DNA was prepared from 26 µl of Anti-5-mC monoclonal antibody 33D3 immunoprecipitated DNA and total DNA respectively using SureTag DNA Labeling Kit acording to manufacturer's protocol (Agilent Technologies) followed by purification using Purification Column provided with the SureTag DNA Labeling Kit. Dye incorporation and DNA yield was measured with NanoDrop 2000.
 
Channel 2
Source name Non-cancerous renal tissue, donor R134
Organism Homo sapiens
Characteristics donor id: donor R134
gender: Female
age: 64
tissue type: Non-cancerous renal tissue
Treatment protocol Tissue samples were obtained from partial or radical nephrectomy material of patients diagnosed with clear cell renal cell carcinoma. None of the patients had preoperatively received radiotherapy, chemotherapy, or hormone therapy.
Extracted molecule genomic DNA
Extraction protocol Renal tissue samples were homogenized using liquid nitrogen and cryoPREP™ CP02 Impactor with tissue TUBE TT1 (Covaris, Woburg, MA, USA). Homogenized tissue powder were treated for up to 18 h at 55 °C with 10-25 μl of proteinase K and 500 μl of lysis buffer, consisting of 50 mM Tris-HCl pH 8.5, 1 mM EDTA, 0.5% Tween-20. DNA was extracted following the standard phenol-chloroform purification and ethanol precipitation protocol.
Label Cy3
Label protocol Cyanine-5 and Cyanine-3 labeled DNA was prepared from 26 µl of Anti-5-mC monoclonal antibody 33D3 immunoprecipitated DNA and total DNA respectively using SureTag DNA Labeling Kit acording to manufacturer's protocol (Agilent Technologies) followed by purification using Purification Column provided with the SureTag DNA Labeling Kit. Dye incorporation and DNA yield was measured with NanoDrop 2000.
 
 
Hybridization protocol 40 µl of each (Cy5 or Cy3) labeled DNA (80 µl in total) was prepared for hybridization using Oligo aCGH/ChIP-Chip Hybridization Kit following manufacturer's protocol (Agilent technologies). Samples were hybridized onto Human DNA Methylation 1×244K Microarrays (Agilent Technologies) for 40 hours at 65°C in a rotating hybridization oven (Agilent Technologies).
Scan protocol Microarrays were scanned immediately after washing using SureScan microarray scanner (Agilent Technologies).
Description DNA methylation profile in non-cancerous renal tissue adjacent primary renal tumor from patient R134
Data processing Scanned images were analyzed with Feature Extraction software v10.7.3.1 (Agilent Technologies) using default parameters (protocol ChIP_107_Sep09 (Read Only), grid 023795_D_F_20140814). Background subtracted and spatially detrended signals were obtained.
 
Submission date Feb 14, 2021
Last update date Feb 15, 2021
Contact name Raimonda Kubiliūtė
E-mail(s) kubiliute.raimonda5@gmail.com
Phone 864128534
Organization name Vilnius University
Department Life Sciences Center
Street address Sauletekio al., 7
City Vilnius
State/province Saulėtekis
ZIP/Postal code 03106
Country Lithuania
 
Platform ID GPL19930
Series (1)
GSE166734 DNA methylation profile of cancerous and non-cancerous renal tissues

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
HsCGHBrightCorner -0.39486876
DarkCorner -0.09737961
A_17_P09887548 0.02795407
A_17_P16734004 -0.29976234
A_17_P31457832 0.83804137
A_17_P32700995 -2.028885
A_17_P17280874 0.7524224
A_17_P16270153 -0.0034256587
A_17_P09200670 -0.92876816
A_17_P25743671 -0.9671143
A_17_P15372775 -1.0527209
A_17_P30271892 0.27380756
A_17_P16795135 1.6595372E-4
A_17_P15532701 0.6750021
A_17_P17091743 0.23205371
A_17_P17318066 0.60498047
A_17_P10947212 1.1269628
A_17_P11110595 -0.47187883
A_17_P27826423 -3.4549563
A_17_P30515985 -0.3074622

Total number of rows: 240952

Table truncated, full table size 6131 Kbytes.




Supplementary file Size Download File type/resource
GSM5082008_R134N.txt.gz 25.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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