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Sample GSM1049702 Query DataSets for GSM1049702
Status Public on Jun 30, 2013
Title early alcohol drinker-1
Sample type RNA
 
Source name Hypo7
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 11.855279
A_52_P580582 198.40619
A_52_P403405 11.876788
A_52_P819156 296.7706
A_51_P331831 229.98706
A_51_P430630 11.93714
A_52_P502357 13.127621
A_52_P299964 22.814392
A_51_P356389 150.56209
A_52_P684402 1034.9994
A_51_P414208 12.04311
A_51_P280918 8789.465
A_52_P613688 633.9154
A_52_P258194 10707.665
A_52_P229271 99.0902
A_52_P214630 2361.7068
A_52_P579519 1797.4336
A_52_P979997 12.250189
A_52_P453864 832.86816
A_52_P655842 62.58282

Total number of rows: 41250

Table truncated, full table size 907 Kbytes.




Supplementary file Size Download File type/resource
GSM1049702_251486821649_S01_GE1_105_Dec08_1_3.txt.gz 9.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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