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Status |
Public on Mar 20, 2014 |
Title |
Transcriptional analysis of live and hybridized J1 and NIH-3T3 cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
J1 mouse embryonic stem cells (mESCs) and NIH-3T3 fibroblasts were grown in standard media conditions. Hybridized cells were fixed with 4% paraformaldehyde; permeabilized in 70% ethanol; incubated for 12 hours at 30C in an RNA preserving hybridization (RPH) buffer (300 mM Sodium chloride, 30mM Sodium citrate, 2.1M Ammonium sulfate, 25% formamide, 10 mM EDTA, 1 mg/ml E. Coli tRNA, 500 μg/ml BSA); and reverse cross-linked for 1 hour at 50C with Sodium dodecyl sulfate (SDS) and Proteinase K (100 mM NaCl, 10 mM Tris pH 8.0, 1 mM EDTA, 0.5% SDS, 500 μg/ml Proteinase K).
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Overall design |
The fold change between J1 and NIH-3T3 cells was compared for live and hybridized samples (one replicate per sample).
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Contributor(s) |
Klemm S, van Oudenaarden A |
Citation missing |
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Submission date |
Mar 14, 2014 |
Last update date |
Nov 01, 2017 |
Contact name |
Sandy Klemm |
E-mail(s) |
[email protected]
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Organization name |
MIT
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Department |
Biology
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Lab |
van Oudenaarden
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Street address |
31 Ames St.
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City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02139 |
Country |
USA |
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Platforms (1) |
GPL11202 |
Agilent-026655 Whole Mouse Genome Microarray 4x44K v2 (Probe Name version) |
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Samples (2) |
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Relations |
BioProject |
PRJNA241310 |