Are you familiar with the Epigenome's Protocols?
Munich's Karin Fellinger & Ulrich Rothbauer protocol "Quantitative immunoprecipitation of GFP-fusion proteins using the GFP-Trap" uses the versatile GFP-Trap to perform immunoprecipitation of fluorescent fusion proteins from cell extracts to identify and map protein-protein interactions.
Tobias Straub of the Adolf Butenandt Institute (Ludwig-Maximilians University, Germany) describes
a method for biologists to get both a rather unbiased look at the quantitative data of their NimbleGen tiling array experiments during initial processing steps and ultimately provide summary tracks of the profiles thus allowing visual browsing of the data and the potential for downstream analyses. See Basic Analysis of NimbleGen ChIP-on-chip Data using Bioconductor/R.
Newest Protocols
- Quantitative immunoprecipitation of GFP-fusion proteins using the GFP-Trap
- Basic Analysis of NimbleGen ChIP-on-chip Data using Bioconductor/R
- In vitro reconstitution of nucleosome arrays with a stoichiometric content of histone octamer and linker histone
- Purification of Human Multiprotein Complexes using OneSTrEP Technology
