|
Status |
Public on May 28, 2014 |
Title |
M010817 |
Sample type |
genomic |
|
|
Channel 1 |
Source name |
Input DNA from M010817 melanoma cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: primary melanoma cells phenotype: Proliferative
|
Growth protocol |
RPMI1640 + 10%FCS + 5 mM glutamine
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted by Dneasy Blood & Tissue Kit (QIAGEN), sheared into 300-500bp fragments by sonication (Covaris), and aliquots 5 ug were incubated with 10 uL of anti-5-methylcytidine antibody (Eurogentec) overnight at 4°C. Antibody-bound DNA was precipated with 40uL of Dynabeeds (M-280 sheep antibody to mouse IgG, Invitrogen) at 4°C for 2 h on a rotating wheel. Bound DNA was eluted by proteinase K incubation for 3 hours at 50°C and purified by standard phenol/chloroform procedure.
|
Label |
Cy3
|
Label protocol |
1.5 ug of MeDIP DNA and 1.5 ug of input DNA were labellled with Cy5 and Cy3 respectively by Nimblegen Dual-Color DNA Labeling Kit
|
|
|
Channel 2 |
Source name |
MeDIP DNA from M010817 melanoma cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: primary melanoma cells phenotype: Proliferative
|
Growth protocol |
RPMI1640 + 10%FCS + 5 mM glutamine
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted by Dneasy Blood & Tissue Kit (QIAGEN), sheared into 300-500bp fragments by sonication (Covaris), and aliquots 5 ug were incubated with 10 uL of anti-5-methylcytidine antibody (Eurogentec) overnight at 4°C. Antibody-bound DNA was precipated with 40uL of Dynabeeds (M-280 sheep antibody to mouse IgG, Invitrogen) at 4°C for 2 h on a rotating wheel. Bound DNA was eluted by proteinase K incubation for 3 hours at 50°C and purified by standard phenol/chloroform procedure.
|
Label |
Cy5
|
Label protocol |
1.5 ug of MeDIP DNA and 1.5 ug of input DNA were labellled with Cy5 and Cy3 respectively by Nimblegen Dual-Color DNA Labeling Kit
|
|
|
|
Hybridization protocol |
Samples were hybridized at 42°C for 20 hours
|
Scan protocol |
Arrays were scanned with MS 200 Microarray Scanner according to manufactorer's protocol
|
Description |
MeDIP on M010817 melanoma cells
|
Data processing |
Arrays were processed with Nimblescan 2.5 standard protocol for MeDIP
|
|
|
Submission date |
May 27, 2014 |
Last update date |
May 28, 2014 |
Contact name |
Phil Fang Cheng |
E-mail(s) |
[email protected]
|
Organization name |
Hopitaux universitaires de Geneve
|
Department |
Oncology
|
Street address |
Rue Gabrielle-Perret-Gentil 4
|
City |
Geneva |
ZIP/Postal code |
1205 |
Country |
Switzerland |
|
|
Platform ID |
GPL15160 |
Series (1) |
GSE57971 |
MeDIP for ten early passage melanoma cell cultures |
|