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Sample GSM5474856 Query DataSets for GSM5474856
Status Public on Oct 05, 2022
Title OMM vs MC2_d8
Sample type RNA
 
Channel 1
Source name primary colon epithelial cells
Organism Mus musculus
Characteristics strain: Germ-free (GF) C57BL/6
cell type: primary colon epithelial cells
treatment: OMM (Oligo-Mouse-Microbiota, community of 12 strains)
time: d8 (day 8) post colonialization
Treatment protocol GF mice were reconstitutted with Oligo-Maus-Mikrobiota (OMM, https://pubmed.ncbi.nlm.nih.gov/27869789/) or minimal consortium (MC2, OMM + E-coli + C. amalonaticus) .
Growth protocol Germ-free (GF) C57BL/6 mice were kept in isolators under sterile conditions.
Extracted molecule total RNA
Extraction protocol Primary murine eithelial cells from colon were isolated by CD45 + cell depletion followed by CD31 + ( Pecam1) positive selection. Total RNA from epithelial cells was isolated with RNeasy (Qiagen) according the supplier's instructions.
Label Cy3
Label protocol RNA labeling was performed with the Low Input Quick-Amp Labeling Kit (Agilent Technologies) according supplier's instructions.
 
Channel 2
Source name primary colon epithelial cells
Organism Mus musculus
Characteristics strain: Germ-free (GF) C57BL/6
cell type: primary colon epithelial cells
treatment: MC2 (OMM + minimal consortium of 2 additional strains, OMM + E.coli + C. amalonaticus)
time: d8 (day 8) post colonialization
Treatment protocol GF mice were reconstitutted with Oligo-Maus-Mikrobiota (OMM, https://pubmed.ncbi.nlm.nih.gov/27869789/) or minimal consortium (MC2, OMM + E-coli + C. amalonaticus) .
Growth protocol Germ-free (GF) C57BL/6 mice were kept in isolators under sterile conditions.
Extracted molecule total RNA
Extraction protocol Primary murine eithelial cells from colon were isolated by CD45 + cell depletion followed by CD31 + ( Pecam1) positive selection. Total RNA from epithelial cells was isolated with RNeasy (Qiagen) according the supplier's instructions.
Label Cy5
Label protocol RNA labeling was performed with the Low Input Quick-Amp Labeling Kit (Agilent Technologies) according supplier's instructions.
 
 
Hybridization protocol Whole mouse genome 8x60K microarrays were done according to the supplier’s protocol (Agilent Technologies).
Scan protocol Scanning of microarrays was performed with 3 µm resolution using a DNA microarray laser scanner (Agilent Technologies)
Description color-swap: polarity(+)
Data processing Raw microarray image data were analyzed with the Image Analysis / Feature Extraction software G2567AA Version A.11.5.1.1 and the GE2_1200_Dec17 extraction protocol (Agilent Technologies). Interarray normalization was done by the mean of trimmed positive non-flagged/non-control reporters.
 
Submission date Jul 27, 2021
Last update date Oct 05, 2022
Contact name Hans-Joachim Mollenkopf
E-mail(s) mollenkopf@mpiib-berlin.mpg.de
Phone +49 30 28460 482
Organization name Max-Planck-Institute for Infection Biology
Lab Microarray/Genomics Core Facility
Street address Charitéplatz 1
City Berlin
ZIP/Postal code 10117
Country Germany
 
Platform ID GPL21810
Series (1)
GSE180907 Fourteen commensals restore immunocompetence in adult germfree mice via maturation of the intestinal vascular system

Data table header descriptions
ID_REF
VALUE LogRatio (base 10) of Cy5/Cy3 intensities

Data table
ID_REF VALUE
1 0.072117277
2 0
3 0
4 -0.034062845
5 0
6 -0.502006867
7 0.216731058
8 -0.034928957
9 -0.011634106
10 0
11 -0.076613466
12 0
13 0.047490105
14 0.031081286
15 0.151073608
16 0
17 -0.003818739
18 0.055798819
19 0.343761257
20 0.018835728

Total number of rows: 62976

Table truncated, full table size 905 Kbytes.




Supplementary file Size Download File type/resource
GSM5474856_US22502595_257480912756_S02_GE2_1200_Dec17_2_3.txt.gz 21.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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