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Sample GSM1125243 Query DataSets for GSM1125243
Status Public on May 28, 2013
Title Dlx3RNAi_iPSCs2
Sample type RNA
 
Source name Induced pluripotent stem cells
Organism Mus musculus
Characteristics treatment: Dlx3 RNAi
strain: OGXICR
gender: female
age: D13.5
tissue: skin
cell type: IPS
Treatment protocol In brief, the limbs and tails of mice were cut off, and the skin was carefully peeled. The isolated mouse skin was then incubated in Collagenase type Ⅳ (2mg/ml, Gibco) for 2hrs at 37℃. After incubation, the epiderm was carefully removed from the surface of the skin. The remaining tissues were dissociated and minced into 1mm pieces, which were then resuspended by Dulbecco’s Modified Eagle Medium (DMEM, Hyclone), containing 10% Fetal bovine serum (Hyclone), 2x penicillin/streptomycin (Invitrogen). The isolated skin fibroblasts were collected by flowing through cell strainers.
Growth protocol Culture in Dulbecco’s Modified Eagle Medium (DMEM, Hyclone), containing 10% Fetal bovine serum (Hyclone), 2x penicillin/streptomycin (Invitrogen). 37℃. The dox-inducible lentiviral system used has been previously described (Maherali et al., 2008). iPSCs were cultured in mESC medium (a 1:1 mixture of Neurolbasal/B27 medium and DMEM/F12 medium supplemented with N2, plus nonessential amino acids, 100 units/ml penicillin, 100 μg/ml streptomycin, 1 mM L-glutamine, 55 μM β-mercaptoethanol, 1 μM PD0325901, and 3 μM CHIR99021) on mitomycin C-treated MEFs. PD0325901 and CHIR99021 could be replaced by LIF (Millipore). The medium was changed every day, and iPSCs were passaged using trypsin (Invitrogen).
Extracted molecule total RNA
Extraction protocol Total cellular RNA was extracted with TRIzol reagent (Sigma). Genomic DNA were removed with DNAase(Ambion). Total RNA was purified with RNeasy plus mini kit(Qiagen).
Label Cy5
Label protocol Total mRNAs of all samples were labeled with Cy5.
 
Hybridization protocol Hybridized to a mouse Oligo Microarray (Phalanx Mouse OneArray® v2, Phalanx Biotech) according to the manufacturer's protocol.
Scan protocol After hybridization, arrays were scanned using GenePix 4000B scanner (Molecular Devices) and processed using the GenePix Pro 6.0 software (Molecular Devices).
Description Induced stem cells
Data processing After removing control probes, the data were analyzed according to the manufacturer's protocol (Phalanx Mouse OneArray® v2, Phalanx Biotech). R1_1, R2_2, G3_iPSCs1, G3_iPSCs2, G6_iPSCs1, G6_iPSCs2, MEF_expression_control1, MEF_expression_control2, Dlx3RNAi_iPSCs1, Dlx3RNAi_iPSCs2 were processed together for normalization.
 
Submission date Apr 17, 2013
Last update date May 28, 2013
Contact name Hongkui Deng
E-mail(s) [email protected]
Organization name Peking University
Street address 5th Yiheyuan Road
City Beijing
ZIP/Postal code 100871
Country China
 
Platform ID GPL13692
Series (2)
GSE43995 Induction of pluripotency in mouse somatic cells with novel factors
GSE47441 Induction of pluripotency in mouse somatic cells with novel factors (expression)

Data table header descriptions
ID_REF
VALUE Quantile normalized signal intensity

Data table
ID_REF VALUE
PH_mM_0002083 32.95454545
PH_mM_0015176 112.0454545
PH_mM_0014801 303.3636364
PH_mM_0011470 38.34090909
mMC007345 446.0909091
mMC021755 23.20454545
PH_mM_0005583 28.52272727
mMC011001 46.95454545
mMC016202 15.5
mMC003657 38.34090909
PH_mM_0007313 44.27272727
PH_mM_0015933 21.90909091
mMC011660 58.5
PH_mM_0002148 66.5
PH_mM_0003069 34.63636364
PH_mM_0000898 21.90909091
PH_mM_0003103 29.06818182
PH_mM_0001625 26.90909091
PH_mM_0001380 25.95454545
PH_mM_0006607 48.72727273

Total number of rows: 14394

Table truncated, full table size 331 Kbytes.




Supplementary file Size Download File type/resource
GSM1125243_Dlx3RNAi_iPSCs2.gpr.gz 2.6 Mb (ftp)(http) GPR
Processed data included within Sample table

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