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Sample GSM1049696 Query DataSets for GSM1049696
Status Public on Jun 30, 2013
Title water group-1
Sample type RNA
 
Source name Hypo1
Organism Mus musculus
Characteristics group: water group
strain: ICR
tissue: Hypothalamus
gender: Male
Treatment protocol On day 51 of the experiment, each mouse is sacrificed by decapitation, and their hypothalami were quickly removed and frozen in N-hexane (−70 °C) for approximately 40 s. The samples were then stored at −80 ◦C until further use.
Growth protocol Before chronic alcohol drinking began, mice (3 weeks old) were allowed to adapt to drinking tubes with both tubes containing water from experimental day 1-5. After adaptation period, mice were randomly aside to 5% alcohol group, 10% alcohol group or water-only control group (n=16-18). For the water-only control group, two drinking tubes in each cage contained deionized water throughout the duration of the experiment. For the alcohol group, one drinking tube contained 5% or 10% alcohol solution while the other contained water.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using the TRIzol reagent (Invitrogen, Carlsbad, CA, USA) and purified with RNeasy column (Qiagen, Valencia, CA).The RNA concentration and purity were analyzed by a Nanodrop spectrophotometer (Nanodrop technologies, Wilmington, DE), with the spectral absorption at 260 and 280 nm. The assessment of the RNA integrity was conducted by the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA). All RNA samples had RNA Integrity Numbers (RIN) of 8.0 or higher.
Label Cy3
Label protocol Total RNA was Cy3 labelled according to Agilent’s Low RNA Input Fluorescent Linear Amplification Kit.
 
Hybridization protocol Hybridized onto Agilent Whole Mouse Genome 4 × 44K G4122F microarrays containing 43 604 probes as described in the manufacturer's protocol.
Scan protocol Slides were scanned (Agilent G2505B) at 5 μm resolution using an extended dynamic range protocol, and images were processed with Agilent Feature Extraction software 9.5.
Description Hypothalamic gene expression from no alcohol exposure mice
Data processing Within-array normalization was performed using the “Background detrending” software (Agilent). The nonuniform outlier features (spots) were removed.
 
Submission date Dec 06, 2012
Last update date Jun 30, 2013
Contact name ke wang
E-mail(s) [email protected]
Phone +86 21 51320288
Organization name Shanghai Biochip Co., Ltd.
Street address 151 Libing Road
City Shanghai
ZIP/Postal code 201203
Country China
 
Platform ID GPL7202
Series (1)
GSE42770 Chronic alcohol consumption from adolescence-to-adulthood in mice — Effect on gene expression in the hypothalamus

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_52_P616356 8.722878
A_52_P580582 218.66887
A_52_P403405 12.689039
A_52_P819156 322.48962
A_51_P331831 293.01794
A_51_P430630 8.622015
A_52_P502357 30.50094
A_52_P299964 25.071243
A_51_P356389 191.74701
A_52_P684402 963.48914
A_51_P414208 8.569264
A_51_P280918 11113.895
A_52_P613688 1122.9111
A_52_P258194 10735.199
A_52_P229271 119.44063
A_52_P214630 4160.601
A_52_P579519 2093.0115
A_52_P979997 8.558192
A_52_P453864 1032.5032
A_52_P655842 83.39218

Total number of rows: 41250

Table truncated, full table size 906 Kbytes.




Supplementary file Size Download File type/resource
GSM1049696_251486821653_S01_GE1_105_Dec08_1_1.txt.gz 9.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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