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Sample GSM2066596 Query DataSets for GSM2066596
Status Public on Feb 20, 2016
Title human colon cancer sw480 cells, control shRNA rep2 [re-analysis]
Sample type RNA
 
Source name human colon cancer SW480 cells treated with lentivirus meditated control shRNA
Organism Homo sapiens
Characteristics cell line: SW480
cell type: human colon cancer cell line
transfected with: lentiviral vector GV248 (hU6-MCS-Ubi-EGFP-IRES-Puro) containing negative control
Treatment protocol The lentiviral vector GV248 (hU6-MCS-Ubi-EGFP-IRES-Puro) containing YWHAE shRNA hairpin sequence (LV-shYWHAE) and negative control were constructed by Shanghai GeneChem, Transfections were performed using polybrene and enhanced infection solution (Genechem,Shang Hai) according to the manufacturer’s recommended protocol when these cells reached 30% confluence.
Growth protocol The human colon cancer cell lines SW480 cells were cultured in DMEM medium(Gibco BRL Co.Ltd.,USA) supplemented with 100 ml/l FBS (Gibco,USA) with the addition of 100 U/ml penicillin and 100 U/ml streptomycin at 37C in a humidified atmosphere of5 % CO2 in air.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol (Invitrogen) according to manufacturer’s instructions. RNA quality and quantity was measured by using nanodrop spectrophotometer (ND-1000, Nanodrop Technologies) and RNA Integrity was determined by gel electrophoresis
Label biotin
Label protocol Synthesis of cDNA and subsequent biotin labeling of cRNA was performed according to the manufacturer´s protocol (GeneChip 3’IVT Express Kit; Affymetrix, Inc.). Briefly, 200 ng of total RNA were converted to cDNA, followed by in vitro transcription and biotin labeling of aRNA
 
Hybridization protocol After fragmentation labeled aRNA was hybridized to Affymetrix PrimeView Human Gene Expression Microarrays for 16h at 45 °C, stained by strepatavidin/phycoerythrin conjugate and scanned as described in the manufacturer´s protocol
Scan protocol Gene ChIP Scanner 3000 7G (Affymetrix Inc.); AGCC (Vers. 3.3)
Description 3683-2_(PrimeView)
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Partek® Genomics SuiteTM. Expression values were RMA normalized, and fold-change values were then calculated using least-squares mean between samples.
 
Submission date Feb 19, 2016
Last update date Feb 20, 2016
Contact name Yousheng Huang
E-mail(s) hys768811@163.com
Organization name Hainan Medical university
Department Department of pathology
Street address The 3rd Xueyuan Road
City Haikou
State/province Hainan
ZIP/Postal code 570102
Country China
 
Platform ID GPL15207
Series (1)
GSE78094 Silcening YWHAE gene expression suppresses the proliferation of colon cancer cells by inducing gene differentially expressed.
Relations
Reanalysis of GSM2066590

Data table header descriptions
ID_REF
VALUE RMA normalized signal intensity

Data table
ID_REF VALUE
11764191_at 0.04483652
11727050_a_at 0.09656334
11750344_a_at -0.113235
11759307_at -0.68210506
11761403_at 0.06918192
11757172_at -0.027120113
11763268_at 0.40630722
11727695_a_at -0.34985447
11730840_a_at -0.28143024
11755175_a_at -0.11610603
11731820_at 0.016905308
11731123_a_at 0.019595146
11761012_x_at 0.034002304
11763593_a_at 0.17965364
11730317_at -0.036998034
11743747_a_at -0.18656206
11716432_a_at 0.15878963
11734196_a_at -0.19609642
11736790_x_at -0.005633116
11745745_a_at -0.9483299

Total number of rows: 49395

Table truncated, full table size 1207 Kbytes.




Supplementary file Size Download File type/resource
GSM2066596_3683-2_PrimeView_.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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