NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3721133 Query DataSets for GSM3721133
Status Public on Apr 13, 2019
Title LNCaP Negative Control
Sample type RNA
 
Source name prostate cancer
Organism Homo sapiens
Characteristics tissue: prostate cancer
cell line: LNCaP
Sex: Male
genotype/variation: control
Extracted molecule total RNA
Extraction protocol RNA was extracted by Absolutely RNA miRNA Kit (Agilent p/n 400814) following the manufacturer’s instructions.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS 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 1.5 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Human miRNA Microarrays (8*60K) 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 dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent Microarray Scanner using oneAgilentG3_miRNA setting for 8x60K array slides.
Data processing The scanned images were analyzed with Agilent Feature Extraction software V.11.5 using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Apr 12, 2019
Last update date Apr 13, 2019
Contact name meng jiao
E-mail(s) jiaomeng851@163.com
Organization name 2nd Hospital of Shandong University
Street address No.247, beiyuan street
City Jinan
ZIP/Postal code 250033
Country China
 
Platform ID GPL25134
Series (1)
GSE129737 MicroRNA expression in CUL4B-depleted LNCaP cells and control

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
dmr_285 6.254958
dmr_3 6.298854
dmr_308 7.350326
dmr_316 6.849776
dmr_31a 6.760476
dmr_6 6.4249644
hsa-let-7a-3p 5.0849648
hsa-let-7a-5p 14.224113
hsa-let-7b-3p 7.0865436
hsa-let-7b-5p 13.676407
hsa-let-7c-3p 4.862587
hsa-let-7c-5p 13.867617
hsa-let-7d-3p 5.3330097
hsa-let-7d-5p 10.548602
hsa-let-7e-3p 4.8577037
hsa-let-7e-5p 9.614023
hsa-let-7f-1-3p 6.9252634
hsa-let-7f-2-3p 5.120403
hsa-let-7f-5p 13.339607
hsa-let-7g-3p 5.315017

Total number of rows: 2555

Table truncated, full table size 60 Kbytes.




Supplementary file Size Download File type/resource
GSM3721133_NC.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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