GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM1209003 Query DataSets for GSM1209003
Status Public on Jan 29, 2014
Title OCIS 28
Sample type RNA
Source name Subject 5005_Anterior_Proximal_Left
Organism Homo sapiens
Characteristics subject id: 5
tissue: vaginal tissue
tissue location (a-p): Anterior
tissue location (p-d): Proximal
tissue location (l-r): Left
Extracted molecule total RNA
Extraction protocol Samples were thawed on ice and mixed by repeat pipet disruption with 70% ethanol according to the procedure described in the technical protocol of the RNeasy Mini Kit (QIAGEN), which was used for subsequent purification according to the manufacturer instructions. This included an on-column DNase digestion with the RNase-free DNase kit (QIAGEN). The total RNAs were eluted once with 50 µL of RNase-free water.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 25ng RNA using the One-Color Low Input Quick Amp Labeling Kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Hybridization protocol 600ng of Cy3-labelled cRNA (specific activity >6.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 25ul containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent SurePrint G3 Human Gene Expression 8x60K v2 arrays (G4851B, Design ID 039494) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then immediately put the slides with Agilent barcode facing up in a slide holder with an ozone-barrier slide cover on top of the array.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505C) using one color scan setting for 8x60K array(Scan Area 61x21.6 mm, Scan resolution 3um, Dye channel is set to Green and Green PMT is set to 100%). Raw data were extracted using the Agilent Feature Extraction software, version, protocol GE1_107_Sep09.
Description vaginal tissue sample
Data processing Microarray expression values were calculated using the gProcessed Signal, which was normalized via log2 transformation and quantile normalization in Partek® Genomics Suite (v.6.6, Partek Inc, St. Louis, MO). Control probe expression levels were removed during normalization. Expression changes due to batch effects between arrays have been removed.
Submission date Aug 14, 2013
Last update date Jan 29, 2014
Contact name Charles David Warden
Organization name City of Hope
Department Department of Molecular and Cellular Biology
Street address 1500 East Duarte Rd
City Duarte
State/province CA
ZIP/Postal code 91010
Country USA
Platform ID GPL17077
Series (1)
GSE49892 Global Expression of Molecular Transporters in the Human Vaginal Tract

Data table header descriptions
VALUE Normalized gene expression

Data table
A_23_P117082 10.7996
A_33_P3246448 2.97408
A_33_P3318220 3.07425
A_33_P3236322 3.15921
A_33_P3319925 3.01942
A_21_P0000509 11.7521
A_21_P0000744 7.21945
A_24_P215804 2.77058
A_23_P110167 12.4622
A_33_P3211513 9.01088
A_23_P103349 1.97026
A_32_P61480 2.63224
A_33_P3788124 2.63751
A_33_P3414202 9.12892
A_33_P3316686 6.99312
A_33_P3300975 3.12286
A_33_P3263061 10.953
A_33_P3261373 2.47057
A_24_P278460 6.8029
A_21_P0013109 2.65649

Total number of rows: 50599

Table truncated, full table size 1058 Kbytes.

Supplementary file Size Download File type/resource
GSM1209003_US92200304_253949410715_S01_GE1_107_Sep09_1_2.txt.gz 3.0 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap