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Sample GSM2936902 Query DataSets for GSM2936902
Status Public on Jun 04, 2018
Title Basal-K5YFP-8w-2 [REANALYSIS]
Sample type RNA
 
Source name YFP+ basal cells of K5CREERT2/RosaYFP mice 8w following tamoxifen administration
Organism Mus musculus
Characteristics tissue: Embryonic mouse mammary gland FACS purified cells
Treatment protocol Pregnant females bearing Lgr5-IRES-GFP embryos were sacrificed at 14 days of gestation and E14 embryos were collected and epidermis + mammary gland were digested in Collagenase+hyaluronidase. Single cells were stained with the appropriate antibodies and FACS sorted.
Growth protocol Mice were maintained in a certified animal house according to European guidelines
Extracted molecule total RNA
Extraction protocol RNA isolation and cDNA amplification was performed as described by Gonzalez-Roca et al. (2010).In brief, 813 or 2000 cells were sorted into lysis buffer and RNA was purified using magnetic beads (RNAClean XP beads, Agencourt).RNA was reverse transcribed and cDNA was amplified using Whole Transcriptome Amplification chemistry (WTA2, Sigma Aldrich). For monitoring amplification, SYBR Green was added to the reaction; it was stopped after 25 cycles when SYBR Green signal reached a plateau. cDNA was purified using Genelute PCR Clean-Up kit (Sigma Aldrich).
Label Biotin
Label protocol cDNA was labeled using GeneChip Mapping 250K Nsp Assay Kit (Affymetrix; catalog # 900766), according to manufacturer's instructions.
 
Hybridization protocol Affymetrix MG-430 PM array strips were hybridized with 8 mg of labeled cDNA, washed, stained and scanned according to the protocol described in GeneAtlas 3’IVT express kit User Manual.
Scan protocol Arrays were scanned with GeneAtlasImaging station scanner (Affymetrix, Santa Clara, CA)
Data processing All the results were normalized using the RMA normalization algorithm using R-bioconductor affy package with standard parameters. Cross experiment normalization was further performed to eliminate the batch effect using non-parametric empirical Bayes frameworks for adjusting data implemented in ComBat function of the Surrogate Variable Analysis package (SVA) in R-bioconductor for the two different microarrays used here and then between this experiment and the previously published data under the accession number GSE69290.
 
Submission date Jan 17, 2018
Last update date Jun 04, 2018
Contact name Alexandra Van Keymeulen
Organization name Université Libre de Bruxelles
Department IRIBHM
Lab Blanpain
Street address 808, route de Lennik CP602
City Bruxelles
ZIP/Postal code 1070
Country Belgium
 
Platform ID GPL11180
Series (2)
GSE109306 Early lineage segregation of multipotent embryonic mammary gland progenitors [expression]
GSE109711 Early lineage segregation of multipotent embryonic mammary gland progenitors
Relations
Reanalysis of GSM1697154

Data table header descriptions
ID_REF
VALUE RMA expression estimate

Data table
ID_REF VALUE
1428118_PM_at
1436602_PM_x_at
1436741_PM_at
1459030_PM_at
1425425_PM_a_at 434.2095094
1428455_PM_at 1293.634028
1460049_PM_s_at 312.619944
1457273_PM_at 1352.374491
1434458_PM_at 481.4022795
1450988_PM_at 1221.381325
1418457_PM_at 2256.20474
1450440_PM_at 931.4147023
1423261_PM_at 473.2552173
1436044_PM_at 350.9463406
1450928_PM_at 376.8882949
1458268_PM_s_at 780.0139877
1423259_PM_at 170.2136054
1418456_PM_a_at 3958.214548
1418666_PM_at 503.4304025
1423062_PM_at 1469.872017

Total number of rows: 45141

Table truncated, full table size 1159 Kbytes.




Supplementary file Size Download File type/resource
GSM2936902_290_2014.ga.cel.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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