NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM940993 Query DataSets for GSM940993
Status Public on Jun 01, 2012
Title OE33_ARID1Aknockdown_biologicalreplicate1
Sample type RNA
 
Source name OE33 cells (esophageal adenocarcinoma cells)
Organism Homo sapiens
Characteristics cell line: OE33
sirna transfection: ON-TARGETplus SMARTpool ARID1A
Treatment protocol Cells were plated in wells in a 6 well-plate (0.2 million cells/well). 24 hours after plating, the cells were transfected using lipofectamin 2000 (Life Technologies, Grand Island, NY, USA) and siRNA (final concentration 50nM). The following siRNAs were used: MS_1 and MS_3 were transfected with ON-TARGETplus SMARTpool ARID1A (Thermo Fisher Scientific, Lafayette, CO, USA), whereas MS_2 and MS_4 were transfected with ON-TARGETplus Non-targeting Pool (Thermo Fisher Scientific). The cells were washed, harvested, and pelleted 48 hours after transfection.
Growth protocol Cells were cultured in 1640 RPMI supplemented with 15% Fetal Bovine Serum
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Rneasy kit (Qiagen, Germantown, MD, USA) according to the manufacturer's manual.
Label Biotin
Label protocol One μg total RNA was combined with 2 μl T7 oligo(dT) primer and 2 μl Poly-A controls and brought to a volume of 12 μl. The samples were incubated at 70ºC for 10 minutes to label as per standard Affymetrix protocol.
 
Hybridization protocol The samples were ice quenched and combined with the hybridization cocktail (5 μl oligonucleotide B2 control, 15 μl 20X eukaryotic hybridization controls, 150 μl 2X hybridization buffer, 30 μl 100% DMSO and 70 μl water). After 10 minutes of pre-hybridizing Human PrimeView array at 45ºC, 60 rpm, 200 μl of cocktail was loaded onto each array and the arrays were hybridized for 16 hours at 45ºC, 60 rpm. The cocktail was removed and the arrays were stained and washed using the Affymetrix GeneChip Fluidics Station 450 and FS450_001 fluidics script.
Scan protocol Fluorescence was detected using the Affymetrix G3000 GeneArray Scanner and image analysis of each GeneChip was perfomed through the Affymetrix GeneChip Command Console version 3.4 (AGCC v3.4) Affymetrix software.
Data processing Data were extracted from the CEL files, RMA normalized and converted to Log2 notation with Partek Genomics Suite (Partek, Missouri, USA). These values were labeled as to ARID1A knockdown status and the groups compared with a standard 1-way ANOVA, Student's t-test.
 
Submission date May 31, 2012
Last update date Jun 01, 2012
Contact name Mirte Mayke Streppel
Organization name Johns Hopkins Hospital
Department Pathology
Lab GI pathology, Maitra lab
Street address 1550 Orleans street, CRBII rm341
City Baltimore
State/province Maryland
ZIP/Postal code 21231
Country USA
 
Platform ID GPL15207
Series (1)
GSE38380 Gene expression data ARID1A knockdown OE33 cells versus mock OE33 cells

Data table header descriptions
ID_REF
VALUE Log2 RMA-normalized signal

Data table
ID_REF VALUE
11715100_at 4.23701
11715101_s_at 7.05188
11715102_x_at 4.81836
11715103_x_at 5.6266
11715104_s_at 5.47815
11715105_at 3.54341
11715106_x_at 4.76264
11715107_s_at 5.91677
11715108_x_at 3.71849
11715109_at 4.66788
11715110_at 4.86754
11715111_s_at 8.0125
11715112_at 3.1882
11715113_x_at 7.62141
11715114_x_at 7.85038
11715115_s_at 3.29814
11715116_s_at 5.50689
11715117_x_at 3.59778
11715118_s_at 3.3946
11715119_s_at 3.57758

Total number of rows: 49372

Table truncated, full table size 1032 Kbytes.




Supplementary file Size Download File type/resource
GSM940993_MStr-CSL-MS_1-1a-PrimeView_PrimeView_.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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