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Sample GSM4490932 Query DataSets for GSM4490932
Status Public on Oct 27, 2020
Title K_2_NS
Sample type RNA
 
Source name Ileum, 21dpi, control, replicate 1
Organism Sus scrofa
Characteristics tissue: Peyer's patches and mesenteric lymph nodes
gender: male
age: 35d
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRIZOL Reagent (Cat#15596-018, Life technologies, Carlsbad, CA, US) following the manufacturer’s instructions and checked for a RIN number to inspect RNA integrity by an Agilent Bioanalyzer 2100 (Agilent technologies, Santa Clara, CA, US). Qualified total RNA was further purified by RNeasy mini kit (Cat#74106, QIAGEN, GmBH, Germany) and RNase-Free DNase Set (Cat#79254, QIAGEN, GmBH, Germany).
Label Cy3
Label protocol Total RNA was amplified and labeled by Low Input Quick Amp Labeling Kit, One-Color (Cat.# 5190-2305, Agilent technologies, Santa Clara, CA, US), following the manufacturer’s instructions. Labeled cRNA were purified by RNeasy mini kit (Cat.# 74106, QIAGEN, GmBH, Germany).
 
Hybridization protocol Each slide was hybridized with 1.65μg Cy3-labeled cRNA using Gene Expression Hybridization Kit (Cat.# 5188-5242, Agilent technologies, Santa Clara, CA, US) in Hybridization Oven (Cat.# G2545A, Agilent technologies, Santa Clara, CA, US), according to the manufacturer’s instructions. After 17 hours 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), followed the manufacturer’s instructions.
Scan protocol Slides were scanned by Agilent Microarray Scanner (Cat#G2565CA, Agilent technologies, Santa Clara, CA, US) with default settings, Dye channel: Green, Scan resolution=5μm, PMT 100%, 10%, 16bit. Data were extracted with Feature Extraction software 10.7 (Agilent technologies, Santa Clara, CA, US). Raw data were normalized by Quantile algorithm, GeneSpring Software 12.6.1 (Agilent technologies, Santa Clara, CA, US).
Description Gene expression at 21dpi without PCV2 infection
Data processing Data were extracted with Feature Extraction software 10.7 (Agilent technologies, Santa Clara, CA, US). Raw data were normalized by Quantile algorithm, limma packages in R.
 
Submission date Apr 22, 2020
Last update date Oct 27, 2020
Contact name Fengyang Shi
E-mail(s) [email protected]
Organization name Beijing University Of Agriculture
Street address No. 7 Beinong Road, Changping District
City Beijing
ZIP/Postal code 102206
Country China
 
Platform ID GPL16571
Series (1)
GSE149144 Ileal gene expression signatures of piglets after PCV2 infection

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner 15.091782
DarkCorner 1.3974122
A_72_P774000 2.7303011
A_72_P650049 4.7421107
A_72_P259407 7.260945
A_72_P718368 7.303733
A_72_P331648 1.3357149
A_72_P225442 7.949004
A_72_P041431 1.3553073
A_72_P652087 9.574151
A_72_P102096 6.4810658
A_72_P382163 4.470677
A_72_P389403 5.066545
A_72_P049701 1.3860201
A_72_P316773 10.585767
A_72_P118766 1.3932225
A_72_P400848 1.3984153
A_72_P144336 1.4023696
A_72_P285724 1.4077815
A_72_P295054 2.1822822

Total number of rows: 43663

Table truncated, full table size 965 Kbytes.




Supplementary file Size Download File type/resource
GSM4490932_K_2_NS.txt.gz 8.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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