Cut out, as coupons

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Possible Answers: CLIP.

Random information on the term “CLIP”:
Crosslinking immunoprecipitation (CLIP) was developed in 2003[1] by the laboratory of Robert B. Darnell as a means of generating genome-wide maps of the binding sites of the Nova RNA binding protein to its RNA targets without disturbing cells (in the case of Nova, this was neurons in the brain). CLIP uses UV light to penetrate cells or tissues, inducing a covalent crosslink between proteins and nucleic acids (but not protein-protein interactions) that are within ~one Ângstrom resolution.[2] The crosslinked RNA protein complexes are then purified, typically using purification with antibodies (e.g. immunoprecipitation), the protein then removed with proteinase K, and the RNA sequenced and mapped back to the transcriptome to identify interaction sites. CLIP is in many ways analogous to DNA-ChIP (Chromatin immunoprecipitation) but provides higher resolution than typical ChIP methods that have been implemented.
Taken from Wikipedia

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