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Sample GSM441228 Query DataSets for GSM441228
Status Public on Mar 09, 2010
Title Neurogenin ChIP-chip on Ciona intestinalis embryo (64-cell stage) Sample 1, Array 1
Sample type genomic
 
Channel 1
Source name Whole Cell Extract (WCE) DNA
Organism Ciona intestinalis
Characteristics fraction: input
antibody: none
Treatment protocol Approximately 3.1 kb of the Neurogenin promoter and the coding region of Neurogenin were cloned into pDONR P4-P1R and pDONR221 (Invitrogen), respectively. cDNA encoding GFP was cloned into pDONR P2R-P3. Recombination of these three plasmids with Multisite Gateway technology (Invitrogen) resulted in a construct encoding GFP-tagged Neurogenin. Fertilized eggs were electroporated with this DNA construct.
Growth protocol C. intestinalis adults were obtained from the national bio-resource project for Ciona intestinalis and were maintained under constant light to induce oocyte maturation. Eggs and sperm were obtained surgically from the gonoduct. Following insemination, eggs were washed and maintained in seawater at 18˚C in Millipore-filtered seawater containing 50ug/ml streptomycin sulfate.
Extracted molecule genomic DNA
Extraction protocol The embryo were fixed with 1% formaldehyde for 15 min. Chromatin was sonicated to obtain DNA fragments with an average of size of 1kb. After reversal of the fixation, the WCE DNA were amplified by LM-PCR.
Label Cy3
Label protocol Amplified DNA was directly labeled by random-primed, Klenow-based extension protocol that is used with CGH Labeling kit (Invitrogen).
 
Channel 2
Source name GFP-tagged Neurogenin ChIP in Ciona intestinalis embryo (64-cell stage)
Organism Ciona intestinalis
Characteristics fraction: IP
embryo: 64-cell stage
construct: GFP-tagged Neurogenin
Treatment protocol Approximately 3.1 kb of the Neurogenin promoter and the coding region of Neurogenin were cloned into pDONR P4-P1R and pDONR221 (Invitrogen), respectively. cDNA encoding GFP was cloned into pDONR P2R-P3. Recombination of these three plasmids with Multisite Gateway technology (Invitrogen) resulted in a construct encoding GFP-tagged Neurogenin. Fertilized eggs were electroporated with this DNA construct.
Growth protocol C. intestinalis adults were obtained from the national bio-resource project for Ciona intestinalis and were maintained under constant light to induce oocyte maturation. Eggs and sperm were obtained surgically from the gonoduct. Following insemination, eggs were washed and maintained in seawater at 18˚C in Millipore-filtered seawater containing 50ug/ml streptomycin sulfate.
Extracted molecule genomic DNA
Extraction protocol The embryo were fixed with 1% formaldehyde for 15 min. Chromatin was sonicated to obtain DNA fragments with an average of size of 1kb. The DNA fragments were enriched by immunoprecipitation with an polyclonal antibody specific for GFP (Invitrogen). After reversal of the fixation, the immunoprecipitated DNA were amplified by LM-PCR.
Label Cy5
Label protocol Amplified DNA was directly labeled by random-primed, Klenow-based extension protocol that is used with CGH Labeling kit (Invitrogen).
 
 
Hybridization protocol Hybridization and washing protocols were according to the manufacturer’s instructions (Agilent Technologies).
Scan protocol The microarrays were scanned with an Agilent G2565BA Microarray Scanner (Agilent Technologies).
Description Neurogenin ChIP-chip on Ciona intestinalis embryo (64-cell stage) Sample 1, Array 1 GFP-tagged Neurogenin ChIP-chip in Whole Genome region in Ciona intestinais embryo (64-cell stage) using polyclonal anti-GFP antibody (Invitrogen)
Data processing The resulting fluorescence intensity for each spot was quantified using Agilent Feature Extraction Software ver. 9.1 (Agilent Technologies).
 
Submission date Aug 17, 2009
Last update date Mar 09, 2010
Contact name Atsushi Kubo
Organization name Kyoto University
Department Department of zoology, Graduate School of Science
Street address Sakyo-ku
City Kyoto
State/province Kyoto
ZIP/Postal code 606-8502
Country Japan
 
Platform ID GPL6555
Series (2)
GSE17689 Neurogenin ChIP-chip on Ciona intestinalis embryo (64-cell stage)
GSE17976 ChIP-chip analysis of the Ciona intestinalis embryo

Data table header descriptions
ID_REF
VALUE normalized log10 ratio Cy5/Cy3

Data table
ID_REF VALUE
4 -7.48E-02
5 2.85E-01
6 -3.21E-01
7 -2.64E-01
8 -5.88E-02
9 1.99E-01
10 -1.14E-01
11 -4.24E-03
12 -3.04E-01
13 8.14E-02
14 -3.84E-02
15 -1.41E-01
16 1.31E-02
17 5.15E-01
18 3.21E-02
19 -1.29E-01
20 -1.04E-01
21 1.37E-01
22 -7.63E-02
23 1.52E-02

Total number of rows: 241700

Table truncated, full table size 3797 Kbytes.




Supplementary file Size Download File type/resource
GSM441228_Neurogenin_ChIP_chip_1-1.txt.gz 51.7 Mb (ftp)(http) TXT
Processed data included within Sample table

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