|
Status |
Public on Feb 14, 2013 |
Title |
Normal colon tissue, NBRCCC026 |
Sample type |
genomic |
|
|
Channel 1 |
Source name |
Normal colon tissue, relapse group
|
Organism |
Homo sapiens |
Characteristics |
tissue: normal colon adjacent to colon cancer age: 52 yr relapse status: relapse
|
Growth protocol |
Tissues were obtained and immediately snap-frozen in liquid nitrogen and stored.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA (gDNA) was prepared using the phenol/chloroform/isoamyl alcohol method.
|
Label |
Cy5
|
Label protocol |
Labeling was performed according to Agilent's recommended protocol. Briefly, 5 μg gDNA was digested with restriction enzymes Alu I (Promega) and Rsa I (Promega), and was labeled fluorescently using the Agilent DNA Labeling kit (Agilent). Patients' gDNAs were labeled with Cy5 and commercial gDNAs as a reference were labeled with Cy3 dUTP, respectively.
|
|
|
Channel 2 |
Source name |
Commerical gDNA
|
Organism |
Homo sapiens |
Characteristics |
sample type: reference
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Control DNA: Promega #G1471 (male) and #G1521 (female).
|
Label |
Cy3
|
Label protocol |
Labeling was performed according to Agilent's recommended protocol. Briefly, 5 μg gDNA was digested with restriction enzymes Alu I (Promega) and Rsa I (Promega), and was labeled fluorescently using the Agilent DNA Labeling kit (Agilent). Patients' gDNAs were labeled with Cy5 and commercial gDNAs as a reference were labeled with Cy3 dUTP, respectively.
|
|
|
|
Hybridization protocol |
The labeled DNA was denatured and pre-annealed with Cot-1 DNA and Agilent blocking reagent and hybridized for 40 hours at 20 rpm in an Agilent hybridization oven.
|
Scan protocol |
The arrays were scanned at 5-㎛ resolution using an Agilent scanner (Agilent), and the image was analyzed with Feature Extraction Software 9.1.1.1. Images were quantified using Agilent Feature Extraction Software.
|
Description |
NBRCCC026
|
Data processing |
Agilent Feature Extraction Software was used for background subtraction and LOWESS normalization.
|
|
|
Submission date |
Feb 13, 2013 |
Last update date |
Feb 14, 2013 |
Contact name |
Park Chan Hee |
E-mail(s) |
[email protected]
|
Phone |
80222277650
|
Organization name |
Cancer Metastasis Research Center
|
Street address |
Shinchondong 134
|
City |
Seodaemun-gu |
State/province |
Seoul |
ZIP/Postal code |
120-752 |
Country |
South Korea |
|
|
Platform ID |
GPL8841 |
Series (1) |
GSE44300 |
DNA profiling of human normal colon tissues |
|