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- B867f02861f42ced13ad07d1d38236c01 hasDbXref "FBC:GM" @default.
- B867f02861f42ced13ad07d1d38236c01 hasDbXref "PMID:11983170" @default.
- B867f02861f42ced13ad07d1d38236c01 hasDbXref "PMID:18255029" @default.
- B867f02861f42ced13ad07d1d38236c01 type Axiom @default.
- B867f02861f42ced13ad07d1d38236c01 annotatedProperty IAO_0000115 @default.
- B867f02861f42ced13ad07d1d38236c01 annotatedSource FBcv_0005052 @default.
- B867f02861f42ced13ad07d1d38236c01 annotatedTarget "Non-fluorescent fragment of a fluorescent protein. A functional fluorophore can be reconstituted if a split fluorescent protein fragment is expressed with a complementary split fluorescent protein fragment and the fragments are brought together in vivo, permitting the study of biological interactions. Protein-protein interactions can be studied using the bimolecular fluorescence complementation (BiFC) technique, where a fluorescent protein is reconstituted if the two complementary split fluorescent protein fragments are fused to interacting proteins or protein domains that bring the split halves together into the same macromolecular complex. Associations between closely apposed cells can be studied if the two complementary split fluorescent protein fragments are tethered to the surface of these cells, for example to study connectivity in the nervous system using the GFP Reconstitution Across Synaptic Partners (GRASP) technique." @default.