|
Status |
Public on Oct 03, 2006 |
Title |
NCCIT human embryonic carcinoma cells |
Sample type |
RNA |
|
|
Source name |
cell line NCCIT
|
Organism |
Homo sapiens |
Characteristics |
human embryonic carcinoma cell line NCCIT
|
Growth protocol |
NCCIT cells were maintained undifferentiated in high-glucose DMEM supplemented with 10% FCS, 2mM L-glutamine, and penicillin-streptomycin.
|
Extracted molecule |
total RNA |
Extraction protocol |
Qiagen RNeasy kit with on-column DNA digestion following the manufacturer's instructions
|
Label |
Cy3
|
Label protocol |
Linear amplification kit Ambion #IL1791 following the manufacturer's instructions. Input amount: 300ng of total RNA; IVT: 6h
|
|
|
Hybridization protocol |
Employing materials and protocols by Illumina Inc.; hybridisation: 17h at 55 degC
|
Scan protocol |
Using an Illumina scanner; gain factor: 2.5
|
Description |
Cells were > 90% undifferentiated as judged by immunocytochemistry using and OCT4 antibody. Data are average intensity values from three replicate cell cultures / hybridisations.
|
Data processing |
In BeadStudio 1.0 raw data were background subtracted and normalised using the "rank invariant" algorithm. Value = "null" denotes expression below background (p < 0.01).
|
|
|
Submission date |
Jul 31, 2006 |
Last update date |
Oct 03, 2006 |
Contact name |
Boris Greber |
E-mail(s) |
boris.greber@mpi-muenster.mpg.de
|
Organization name |
Max Planck Institute for Molecular Biomedicine
|
Department |
Cell and Developmental Biology
|
Street address |
Röntgenstraße 20
|
City |
Münster |
ZIP/Postal code |
48149 |
Country |
Germany |
|
|
Platform ID |
GPL2700 |
Series (1) |
GSE5416 |
Comparative transcriptome analysis of four cell lines |
|