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Sample GSM3518689 Query DataSets for GSM3518689
Status Public on Dec 19, 2018
Title 3: Eutopic endometrium of the normal group
Sample type RNA
 
Source name Eutopic endometrium
Organism Homo sapiens
Characteristics tissue: Eutopic endometrium
gender: female
age: 51y
diagnosis: normal
Treatment protocol The isolated tissues were stored in cryobiolgical inventory system in 10 minutes to avoid the total RNA extraction
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.
Description MicroRNA expression of the normal group
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 Dec 18, 2018
Last update date Dec 19, 2018
Contact name min juan liu
Organization name ZhuJiang Hospital of Southern Medical University
Street address gong ye da dao No.253
City Guangzhou
ZIP/Postal code 510000
Country China
 
Platform ID GPL25134
Series (1)
GSE124010 miR-205-5p Inhibits Human Endometriosis Progression by Targeting ANGTP2 in Endometrial Stromal Cells

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
hsa-let-7a-3p 2.85
hsa-let-7a-5p 15.22
hsa-let-7b-3p 3.85
hsa-let-7b-5p 14.87
hsa-let-7c-3p 2.61
hsa-let-7c-5p 13.18
hsa-let-7d-3p 3.10
hsa-let-7d-5p 11.58
hsa-let-7e-3p 2.76
hsa-let-7e-5p 11.31
hsa-let-7f-1-3p 3.96
hsa-let-7f-2-3p 2.81
hsa-let-7f-5p 14.26
hsa-let-7g-3p 2.66
hsa-let-7g-5p 13.32
hsa-let-7i-3p 3.31
hsa-let-7i-5p 12.23
hsa-miR-1-3p 3.30
hsa-miR-1-5p 2.85
hsa-miR-100-3p 2.96

Total number of rows: 2549

Table truncated, full table size 49 Kbytes.




Supplementary file Size Download File type/resource
GSM3518689_3_257015614423_S01_miRNA_107_Sep09_105_1_3.txt.gz 7.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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