Puf proteins, RNA co-immunopurification
Source: NCBI BioProject (ID PRJNA104871)
Source: NCBI BioProject (ID PRJNA104871)
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Project name: Saccharomyces cerevisiae
Description: RNA-coimmunopurifications with TAP-tagged Puf proteins from Saccharomyces cereviseae. Untagged strain (BY4741) served as a control. Cells were grown to midlog phase and harvested by centrifugation. TAP-tagged Puf proteins were affinity purified from cell-free extracts with IgG sepharose and eluted with TEV protease. RNA was isolated from extract (=input)and from purified protein samples by phenol-chloroform extraction. RNA samples were reverse transcribed using a mixture of oligo-dT and random nonamer oligos in the presence of amino-allyl dUTP/ dNTP mixture. cDNAs were fluorescently labeled and hybridized on yeast DNA microarrays over night at 65 degrees. For a detailed procedure see http://microarray-pubs.stanford.edu/yeast_puf and also Gerber AP et al. PLoS Biology, 2004.Set of arrays organized by shared biological context, such as organism, tumors types, processes, etc.Keywords: Logical SetOverall design: Computed
Data type: Transcriptome or Gene expression
Sample scope: Multiisolate
Relevance: ModelOrganism
Organization: Stanford University, School of Medicine, Stanford Microarray Database (SMD)
Literatures
- PMID: 15024427
Release date: 2006-01-04
Last updated: 2006-01-03