|
Status |
Public on Dec 10, 2012 |
Title |
XY23 |
Sample type |
RNA |
|
|
Source name |
NPC biopsy
|
Organism |
Homo sapiens |
Characteristics |
disease state: nasopharyngeal carcinoma
|
Biomaterial provider |
Department of Pathology, Guangdong Medical College
|
Extracted molecule |
total RNA |
Extraction protocol |
8 micron cryosections were transferred onto PALM membrane slides (P.A.L.M. Microlaser Technologies) and air dried on ice for about 1 minute. Slides were immersed for 2 minutes in cold 75% ethanol, tapped dry and stained for 30 seconds in cold haematoxylin and eosin (9:1) containing 1% NucleoGuard (AmpTec, Hamburg). Excess stain was tapped off and slides were washed in cold nuclease-free water for 30 seconds, cold 75% ethanol for 1 minute, cold 100% ethanol for 1 minute then air dried. Tumour cells for analysis were excised by laser microdissection and pressure catapulting using a PALM MicroBeam instrument and caught on PALM Adhesive Caps. A minimum of 200,000 µm2 of tissue was collected for each DNA or RNA extraction. RNA was extracted by adding 100µl of RLT buffer (Qiagen) supplemented with 1µl of N-carrier (AmpTec) and 1 µl of NucleoGuard followed by incubation at room temperature for 15 minutes. Extracted RNA was cleaned up using a Qiagen RNeasy mini kit, including the on-column DNase step as per the manufacturer’s instructions.
|
Label |
biotin
|
Label protocol |
The eluted RNA was collected by ethanol precipitation in the presence of 1 µl P-carrier (AmpTec), washed twice with 80% ethanol and subjected to three rounds of amplification followed by biotin labelling using an ExpressArt TR Nano amplification kit (AmpTec) and an Affymetrix IVT labelling kit.
|
|
|
Hybridization protocol |
Biotinylated RNA was fragmented and hybridised to Affymetrix Human Genome U133Plus2 Arrays according to the Affymetrix protocol.
|
Scan protocol |
All arrays were washed and stained on an Affymetrix FS450 fluidics station then scanned using an Affymetrix GeneChip 3000 7G scanner as per Affymetrix procedures.
|
Data processing |
Expression array data were analysed with GCOS using the default settings except that the target signal was set to 100.
|
|
|
Submission date |
Dec 19, 2011 |
Last update date |
Dec 10, 2012 |
Contact name |
Wenbin Wei |
E-mail(s) |
Wenbin.Wei2@durham.ac.uk
|
Organization name |
Durham University
|
Department |
Biosciences
|
Street address |
Stockton Road
|
City |
Durham |
ZIP/Postal code |
DH1 3LE |
Country |
United Kingdom |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE34573 |
A Global View of the Oncogenic Landscape in Nasopharyngeal Carcinoma:An Integrated Analysis at the Genetic and Expression Levels |
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