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Sample GSM1831947 Query DataSets for GSM1831947
Status Public on Jul 25, 2015
Title Liver_CS_rep3
Sample type RNA
 
Source name Liver, CS group, replicate 3
Organism Sus scrofa
Characteristics breed: Duroc × Landrace × Large White
tissue: liver
gender: male
age: 170 d
Treatment protocol The liver and colonic mucosa tissues were collected and preserved in liquid nitrogen.
Growth protocol Pigs in the control group were offered a corn/soybean-based diet, while 230 g/kg purified corn starch (CS) was replaced with purified RPS in the RPS diet group. Diets were formulated according to the nutrient requirements of the National Research Council (1998). When animals reached the age of 120 days, diets were adapted to the nutrient requirements of the animals (finishing diet) and the amount of purified starch increased to 280 g of CS or RPS per kilogram of feed. Pigs had unlimited access to feed and water throughout the experimental period, which consisted of two 50-day trials in which the pigs consumed the growing diet (days 0-50) and finishing diet (days 51-100), respectively.
Extracted molecule total RNA
Extraction protocol The total RNA was extracted using the TRIzol reagent (Life Technologies, Carlsbad, CA, USA) according to the manufacturer’s instructions and then checked for RNA integrity and purity using an Agilent Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA, USA). The total qualified RNA was further purified using an RNeasy mini kit (QIAGEN, GmBH, Germany) and an RNase-Free DNase Set (QIAGEN, GmBH, Germany). Only those samples that had an OD260/OD280 ratio of approximately 2.0 and showed no degradation (RNA integrity number ≥ 7.0) were used to generate labeled targets.
Label Cy3
Label protocol The total RNA was amplified and labeled using a Low Input Quick Amp Labeling Kit (Agilent Technologies, Santa Clara, CA, USA), following the manufacturer’s instructions.
 
Hybridization protocol Each slide was hybridized with 1.65μg Cy3-labeled cRNA using a Gene Expression Hybridization Kit (Agilent technologies, Santa Clara, CA, USA) in a hybridization oven.
Scan protocol After 17 h of hybridization, the slides were washed with a Gene Expression Wash Buffer Kit (Agilent technologies, Santa Clara, CA, USA), according to the manufacturer’s instructions. The slides were then scanned on an Agilent Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA).
Description Gene expression in the liver of pigs fed CS diet
Data processing data was extracted using Feature Extraction Software 10.7 (Agilent Technologies, Santa Clara, CA, USA). The raw data was normalized using a quantile algorithm, Gene Spring Software 11.0 (Agilent Technologies, Santa Clara, CA, USA).
 
Submission date Jul 24, 2015
Last update date Jul 25, 2015
Contact name Yong Su
E-mail(s) [email protected]
Organization name Nanjing Agricultural University
Street address Weigang 1#
City Nanjing
ZIP/Postal code 210095
Country China
 
Platform ID GPL16571
Series (1)
GSE71305 Effects of long-term intake of RPS on gene expression in the colon and liver of pigs

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_72_P000001 0.89824426
A_72_P000006 6.428874
A_72_P000036 8.93516
A_72_P000041 0.7632188
A_72_P000051 1.1495912
A_72_P000056 3.1539454
A_72_P000061 1.5146874
A_72_P000071 0.9845864
A_72_P000076 2.2583594
A_72_P000086 0.93207407
A_72_P000106 3.0032487
A_72_P000111 8.852218
A_72_P000131 4.2625866
A_72_P000136 0.9933317
A_72_P000146 1.2379937
A_72_P000156 2.5160072
A_72_P000171 9.833037
A_72_P000176 6.0908136
A_72_P000186 4.3738866
A_72_P000196 1.2041714

Total number of rows: 43603

Table truncated, full table size 964 Kbytes.




Supplementary file Size Download File type/resource
GSM1831947_Liver_A_3.txt.gz 8.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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