NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3526795 Query DataSets for GSM3526795
Status Public on Dec 03, 2019
Title Healthy volunteer-6
Sample type RNA
 
Source name Peripheral Blood
Organism Homo sapiens
Characteristics tissue: whole blood
diagnosis: healthy
Extracted molecule total RNA
Extraction protocol Not provided
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 Whole Human Genome Oligo Microarrays (G4112A) 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 DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
Description Gene expression in human blood
Data processing The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters (protocol GE1-v1_91 and Grid: 012391_D_20060331) 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 21, 2018
Last update date Dec 03, 2019
Contact name Yi Wang
E-mail(s) yiwang1984@hotmail.com
Organization name Sichuan Provincial Orthopedic Hospital
Department Cervicodynia/Omalgia/Lumbago/Sciatica Department 2
Street address 132 West First Section First Ring Road
City Chengdu
State/province Sichuan
ZIP/Postal code 610041
Country China
 
Platform ID GPL21185
Series (1)
GSE124272 Transcriptome signatures reveal candidate key genes in the whole blood of patients with lumbar disc prolapse

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_22_P00017253 1.272327875
A_23_P347169 1.530494359
A_21_P0001361 2.1497951
A_22_P00011001 2.344584406
A_33_P3307795 1.543476375
A_33_P3360863 3.126208479
A_21_P0011200 1.447675637
A_23_P396867 6.952364409
A_33_P3394769 14.52907448
A_33_P3273073 2.141061088
A_23_P21324 0.656853244
A_33_P3395513 4.42857513
A_23_P208636 1.152384176
A_21_P0010440 4.504170274
A_33_P3217500 2.302359609
A_24_P100996 0.816917767
A_33_P3250953 5.233056532
A_21_P0008526 0.806375309
A_33_P3373573 0.968782281
A_23_P370544 5.147149201

Total number of rows: 58341

Table truncated, full table size 1463 Kbytes.




Supplementary file Size Download File type/resource
GSM3526795_volunteer-6_257236318210_S001_GE1_1200_Jun14_2_4.txt.gz 12.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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