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Sample GSM1049703 Query DataSets for GSM1049703
Status Public on Jun 30, 2013
Title early alcohol drinker-2
Sample type RNA
 
Source name Hypo8
Organism Mus musculus
Characteristics group: early alcohol drinker
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 after chronic alcohol consumption from adolescence-to-adulthood in mice, which was an early high alcohol drinker
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 5.300265
A_52_P580582 211.03427
A_52_P403405 12.294001
A_52_P819156 303.07925
A_51_P331831 234.75063
A_51_P430630 5.665542
A_52_P502357 28.86702
A_52_P299964 44.600903
A_51_P356389 174.62286
A_52_P684402 1062.64
A_51_P414208 5.4505763
A_51_P280918 10209.807
A_52_P613688 785.66693
A_52_P258194 10477.204
A_52_P229271 135.49544
A_52_P214630 3907.2146
A_52_P579519 2049.9666
A_52_P979997 5.8385997
A_52_P453864 951.25366
A_52_P655842 96.990654

Total number of rows: 41250

Table truncated, full table size 907 Kbytes.




Supplementary file Size Download File type/resource
GSM1049703_251486821649_S01_GE1_105_Dec08_1_4.txt.gz 9.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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