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Sample GSM4826333 Query DataSets for GSM4826333
Status Public on Oct 10, 2020
Title Mammary gland cow Jurassienne_Control
Sample type RNA
 
Source name Mammary gland before restriction
Organism Bos taurus
Characteristics breed: Holstein cow
animal id: Jurassienne
diet: CONT
tissue: Mammary gland biopsy
Treatment protocol During the control period (CONT) before restriction, all cows were allowed ad libitum intake of a lactation diet. During the restriction period (REST), feed allowance was reduced to meet 50% of NEL requirements calculated from body weight, feed intake and milk production and composition recorded before restriction. Mammary gland (MG) samples were collected by biopsies on day 0 and day 6 relative to initiation of feed restriction. Mammary biopsies were performed after the selection of the biopsy site at a midpoint on a rear quarter. Approximately 600–650 mg of tissue was collected, rinsed in sterile 0.9% saline solution, snap-frozen in liquid nitrogen, and stored at −80 °C until RNA extraction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from approximately 50 mg of MG biopsies using the miRVana kit (Thermo Fisher Scientific, USA). The concentration and quality of the RNAs were estimated by spectrophotometry Nanodrop TH (ND-1000, NanoDrop Technologies LLC, Wilmington, DE, USA) and using the Bioanalyzer 2100 (Agilent Technologies Inc., Santa Clara, CA, USA), respectively.
Label Cy3
Label protocol 50 ng of total RNA extracted were amplified and fluorescently labelled to produce Cy3 cRNA using the Low Input Quick Amp Labeling one color Kit (Agilent, USA) in the presence of spike-in one color control.
 
Hybridization protocol After purification (Qiagen RNeasy Mini Kit), 1,65 µg of Cy3 labeled cRNA were hybridized onto G2519F-023647 Bovine (V2) Gene Expression Microarray, 4x44K (Agilent, USA) with hybridization buffer (Agilent Gene Expression Hybridization Kit) according to the manufacturer’s instructions. After 17h of hybridization, slides were washed with the Gene Expression Wash Pack.
Scan protocol Microarrays were scanned using the Agilent Microarray Scanner G2505 version B (Agilent Technologies, Inc. Santa Clara, CA, USA).
Description Jurassienne CONT
Gene expression before restriction
Data processing The resulting TIFF images (Tagged Image File Format) were processed using Feature Extraction software Version 11. Microarrays were analyzed to determine differential gene expression (DEG) at the mRNA level using GeneSpring software, and data were normalized with 75th percentile shift followed by t-tests moderated with the Benjamini-Hochberg (FDR) correction, Significance was considered at Padj < 0.10.
 
Submission date Oct 09, 2020
Last update date Oct 10, 2020
Contact name Christine LEROUX
E-mail(s) christine.leroux@inrae.fr
Organization name INRAE
Lab Christine LEROUX
Street address Route de Theix
City St Genès-Champanelle
ZIP/Postal code 63122
Country France
 
Platform ID GPL11648
Series (1)
GSE159302 Effects of restriction on mammary gland transcriptome

Data table header descriptions
ID_REF
VALUE Normalized Cy3 signal intensity (gProcessedSignal)

Data table
ID_REF VALUE
1 8.638607e+003
2 4.797233e+000
3 4.814597e+000
4 4.830450e+000
5 4.844220e+000
6 4.856406e+000
7 4.867039e+000
8 4.876049e+000
9 4.883364e+000
10 4.888952e+000
11 4.893079e+000
12 5.067559e+002
13 1.532388e+001
14 4.897017e+000
15 9.088339e+001
16 4.892483e+000
17 4.888077e+000
18 4.882305e+000
19 4.875891e+000
20 4.868165e+000

Total number of rows: 45220

Table truncated, full table size 872 Kbytes.




Supplementary file Size Download File type/resource
GSM4826333_lame3_1029_a3_jurasienneB1.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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