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Sample GSM160168 Query DataSets for GSM160168
Status Public on Feb 06, 2007
Title Tabby (14.5BS) a(16012201010031)
Sample type RNA
 
Channel 1
Source name Tabby (14.5BS) a
Organism Mus musculus
Characteristics Strain: C57BL/6J-Aw-J-EdaTa-6J/J
Gender: male
Age: 14.5dpc
Development stage: embryo
Genetic modification: Mutant Mice
Biomaterial provider Chang-Yi Cui
Growth protocol The UMRR is provided in a solution of 70% ethanol and 0.1 M sodium acetate. Prepare the UMRR for use as follows: 1.Centrifuge the tube at 12,000 x g for 15 minutes at 4C. 2.Carefully remove the supernatant. 3.Wash the pellet in 70% ethanol. 4.Centrifuge the tube at 12,000 x g for 15 minutes at 4C. 5.Carefully remove the supernatant and air-dry the pellet at room temperature for 30 minutes to remove retained ethanol. 6.Resuspend the pellet in RNase-free water to the desired concentration.
Extracted molecule total RNA
Extraction protocol RNA samples from embryonic skin were subjected to LiCl precipitation after Triazol isolation to eliminate genomic DNA contamination. LiCl precipitation was effective for cleaning RNA samples, which is proven in real-time PCR.
Label Cy3
Label protocol Total RNA was labeled using Agilents Fluorescent Linear Amplification kit, according to manufacturers instructions (Product Number G2554A or P/N G2556-66002, Version 3.0, June 2002).
 
Channel 2
Source name Universal Mouse Reference RNA
Organism Mus musculus
Characteristics Universale Mouse Reference
Growth protocol The UMRR is provided in a solution of 70% ethanol and 0.1 M sodium acetate. Prepare the UMRR for use as follows: 1.Centrifuge the tube at 12,000 x g for 15 minutes at 4C. 2.Carefully remove the supernatant. 3.Wash the pellet in 70% ethanol. 4.Centrifuge the tube at 12,000 x g for 15 minutes at 4C. 5.Carefully remove the supernatant and air-dry the pellet at room temperature for 30 minutes to remove retained ethanol. 6.Resuspend the pellet in RNase-free water to the desired concentration.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from cultured cells using a Stratagene Absolutely RNA kit. DNase-treated total RNA samples from 11 cultured cell lines derived from embryo, embryo fibroblast, kidney, liver/hepatocyte, lung/alveolar macrophage, B-lymphocyte, T-lymphocyte (thymus), mammary gland, muscle myoblast, skin, and testis were pooled in equal parts
Label Cy5
Label protocol Total RNA was labeled using Agilents Fluorescent Linear Amplification kit, according to manufacturers instructions (Product Number G2554A or P/N G2556-66002, Version 3.0, June 2002).
 
 
Hybridization protocol Agilent 60-mer oligo microarray processing protocol (SSC Wash/SureHyb Chamber set-up) V4.1, April 2004. Agilent Publication Number: G4140-90030 V4.1 APRIL 2004. The manual can be found at https://www.chem.agilent.com/scripts/literaturePDF.asp?iWHID=34961, or through a WEB search on the manual title.
Scan protocol Slides were scanned with an Agilent DNA Microarray Scanner model G2505-64120 at 100% PMT in both channels, with a scan resolution of 10um. A scan window of 61 x 21.6 mm was used, then images were cropped to size and saved in a modified two-color TIFF format. Images were examined visually for evidence of foreign debris or major failures. Agilent Microarray Scanner User Manual (6.3) http://www.chem.agilent.com/scripts/literaturePDF.asp?iWHID=33696
Description Tabby (14.5BS)
Data processing Data are extracted with Agilent Feature Extraction Software.The data were further processed with NIA ANOVA tool utilities.See http://lgsun.grc.nia.nih.gov/ANOVA for details.
 
Submission date Feb 05, 2007
Last update date Feb 05, 2007
Contact name Minoru S.H. Ko
E-mail(s) kom@mail.nih.gov
Phone 410-558-8359
Organization name NIH
Department National Institute on Aging
Lab Lab of Genetics
Street address 251 Bayview Blvd, Suite 100, 10C
City Baltimore
State/province MD
ZIP/Postal code 21224
Country USA
 
Platform ID GPL2550
Series (1)
GSE6952 Ectodysplasin regulates the lymphotoxin-beta pathway for hair differentiation

Data table header descriptions
ID_REF Feature Number (FeatureNum)
VALUE The normalized VALUE among all the arrays in the series. It is caculated with the following method: (1) Take values from the columns gDyeNormSignal,rDyeNormSignal in the raw files and log-transform them using: log10(max(x,1)). These values will be referenced below as Xgi and Xri where i is array number. (2) Take average of Xri's for the oligo among 36 arrays in the series: AverXr = average(Xri). (3) For each array estimate Yi = Xgi-Xri+AverXr (4) Round Yi to 4 decimal digits. This is used as the normalized VALUE. More detailed information with error correction can be found at http://lgsun.grc.nia.nih.gov/ANOVA/help.html#arrayjoin

Data table
ID_REF VALUE
3 2.9535
4 2.1457
5 3.7741
6 3.3852
8 2.5550
9 2.3632
10 2.4917
12 2.3960
13 3.2213
15 2.0000
16 2.5327
17 2.3019
18 3.1184
19 2.0001
20 2.0118
22 2.8799
23 2.3543
24 2.0982
25 2.0763
26 2.2205

Total number of rows: 41920

Table truncated, full table size 522 Kbytes.




Supplementary file Size Download File type/resource
GSM160168.tif.gz 23.1 Mb (ftp)(http) TIFF
GSM160168.txt.gz 10.4 Mb (ftp)(http) TXT

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