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Sample GSM1835358 Query DataSets for GSM1835358
Status Public on Jul 30, 2016
Title control_knee joint cartilage_male_8 weeks
Sample type RNA
 
Source name knee joint cartilage, eight weeks old
Organism Mus musculus
Characteristics genotype: wildtype
tissue: knee joint cartilage
gender: male
age: 8 weeks old
Treatment protocol knee articular cartilage from 2 months old Col2a1Tsc1KO and control mice was peeled off and washed in sterile and RNase free 0.1M PBS buffer.
Growth protocol All mice were housed in a pathogen-free animal facility.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified using mirVana™ miRNA Isolation Kit without phenol (Cat # AM1561, Ambion, Austin, TX, US), following the manufacturer’s instructions and checked for a RIN number to inspect RNA integration by an Agilent Bioanalyzer 2100 (Agilent technologies, Santa Clara, CA, US).
Label Cy3
Label protocol miRNA molecular in total RNA was labeled by miRNA Complete Labeling and Hyb Kit (Cat # 5190-0456, Agilent technologies, Santa Clara, CA, US) followed the manufacturer’s instructions, labeling section.
 
Hybridization protocol Each slide was hybridized with 100ng Cy3-labeled RNA using miRNA Complete Labeling and Hyb Kit (Cat # 5190-0456, Agilent technologies, Santa Clara, CA, US) in hybridization Oven (Cat # G2545A, Agilent technologies, Santa Clara, CA, US) at 55°C,20 rpm for 20 hours according to the manufacturer’s instructions, hybridization section. After hybridization, slides were washed in staining dishes (Cat # 121, Thermo Shandon, Waltham, MA, US) with Gene Expression Wash Buffer Kit (Cat #5188-5327, Agilent technologies, Santa Clara, CA, US).
Scan protocol Slides were scanned by Agilent Microarray Scanner (Cat # G2565CA, Agilent technologies, Santa Clara, CA, US) and Feature Extraction software 10.7 (Agilent technologies, Santa Clara, CA, US) with default settings.
Description miRNA expression in knee joint cartilage
Data processing Slides were scanned by Agilent Microarray Scanner (Cat # G2565CA, Agilent technologies, Santa Clara, CA, US) and Feature Extraction software 10.7 (Agilent technologies, Santa Clara, CA, US) with default settings. Raw data were normalized by Quantile algorithm, Gene Spring Software 12.6 (Agilent technologies, Santa Clara, CA, US).
 
Submission date Jul 29, 2015
Last update date Jul 30, 2016
Contact name hua wang
E-mail(s) [email protected]
Organization name southern medical university
Department cell biology
Street address gongzhou dadao bei
City guanghzou
State/province guangdong
ZIP/Postal code 510515
Country China
 
Platform ID GPL17912
Series (1)
GSE71484 Investigation of miRNA expression signatures in mTORC1 -stimulated osteoarthritis

Data table header descriptions
ID_REF
VALUE Quantile normalized signal

Data table
ID_REF VALUE
Blank -3.263909
NC1_00000197 -3.263909
NC1_00000215 -3.263909
NC2_00079215 -3.263909
NC2_00092197 -3.263909
NC2_00106057 -3.263909
NC2_00122731 -3.263909
NegativeControl -3.263909
dmr_285 11.563673
dmr_3 14.151848
dmr_308 -3.263909
dmr_316 -3.263909
dmr_31a 10.730499
dmr_6 13.472952
hur_1 14.273754
hur_2 16.387945
hur_4 12.351141
hur_5 -3.263909
hur_6 13.966811
miRNABrightCorner30 12.503365

Total number of rows: 1268

Table truncated, full table size 30 Kbytes.




Supplementary file Size Download File type/resource
GSM1835358_49__254606510531_S01_miRNA_107_Sep09_105_1_1.txt.gz 7.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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