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Sample GSM8068030 Query DataSets for GSM8068030
Status Public on Apr 01, 2024
Title CRF509
Sample type RNA
 
Source name Human peripheral blood
Organism Homo sapiens
Characteristics tissue: Peripheral blood
cell type: Monocytes
participant group: Non-pregnant
Extracted molecule total RNA
Extraction protocol Sample processing: 1 x 106 of monocytes were washed with 1 ml RPMI 1640/Glutamax and centrifuged at 8,000 x g for 4 mins. The cells were re-suspended with diluted RLT buffer (Qiagen, UK) (1/3 with RNase-free water; Invitrogen) to 10,000 cells / μl, and frozen at -80°C.
Label n.a.
Label protocol Sample RNA is hybridised with target-specific capture and reporter probes in order to create a library of unique target-probe complexes. Each target is labelled with a specific molecular barcode, which can then be detected and counted using an automated fluorescence microscope
 
Hybridization protocol RNA samples stored at -80°C were thawed on ice prior to hybridisation reactions. Reporter probes were diluted in 70 μl of hybridisation buffer and gently mixed to create a master mix. To set up the hybridisation reactions, 5 μl of each sample was added to 8 μl of master mix. Hybridisation reactions were then completed by adding 2 μl of Capture ProbeSet and incubation at 65°C for 20 h. Probe set-target RNA hybridisation solution is then further diluted to a final volume of 35 μl. 33 μl of the diluted hybridisation solution is loaded onto a SPRINT microfluidic cartridge, with an air bubble also inserted to the stop point.
Scan protocol Detection and scanning were performed by the nCounter® SPRINT Profiler analysis system (Nanostring).
Description CRF509
Data processing Data analysis was performed using the advanced analysis package (2.0.134) within the nSolver© analysis software (Version 4.0, NanoString©), and differential expression p-value adjustment was done with Benjamini-Hochberg. Significant gene changes were determined to be p ≤ 0.05 with a fold change of ≤ -0.5 or ≥0.5.
 
Submission date Feb 07, 2024
Last update date Apr 01, 2024
Contact name April Rees
E-mail(s) april.rees@swansea.ac.uk
Phone 01792987806
Organization name Swansea University
Street address Room 203 ILS1, Singleton Park
City Swansea
ZIP/Postal code SA2 8PP
Country United Kingdom
 
Platform ID GPL33903
Series (1)
GSE255271 Immunometabolic adaptation in monocytes underpins functional changes during pregnancy [metabolism]

Data table header descriptions
ID_REF
VALUE normalized signal intensity

Data table
ID_REF VALUE
A2M 20
AADAT 20
AANAT 20
ABL1 199.52
ACAA2 457.16
ACACA 34.87
ACACB 35.84
ACADL 20
ACAP2 1627.19
ACAT1 87.17
ACAT2 167.56
ACMSD 20
ACOT12 20
ACOX1 735.14
ACSF3 38.74
ACY1 20
ADA 246.02
ADAL 23.25
ADH1A 20
ADH1B 20

Total number of rows: 782

Table truncated, full table size 8 Kbytes.




Supplementary file Size Download File type/resource
GSM8068030_20210608_30102603060422-01_CRF509_09.RCC.gz 8.7 Kb (ftp)(http) RCC

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