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Sample GSM1049697 Query DataSets for GSM1049697
Status Public on Jun 30, 2013
Title water group-2
Sample type RNA
 
Source name Hypo2
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 6.2336264
A_52_P580582 208.22386
A_52_P403405 6.255346
A_52_P819156 281.86578
A_51_P331831 319.42218
A_51_P430630 6.2982044
A_52_P502357 29.805845
A_52_P299964 31.877914
A_51_P356389 189.01906
A_52_P684402 1003.7059
A_51_P414208 6.351376
A_51_P280918 8469.507
A_52_P613688 596.5054
A_52_P258194 10126.708
A_52_P229271 127.59961
A_52_P214630 2936.8015
A_52_P579519 1754.8965
A_52_P979997 6.4361887
A_52_P453864 841.9581
A_52_P655842 90.27228

Total number of rows: 41250

Table truncated, full table size 907 Kbytes.




Supplementary file Size Download File type/resource
GSM1049697_251486821653_S01_GE1_105_Dec08_1_2.txt.gz 9.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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