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- Tetrafluorophenyl_esters abstract "Tetrafluorophenyl (TFP) esters chemistry typically used to attach fluorophores or haptens to the primary amines of biomolecules. They produce as strong amide bound than succinimidyl esters (SE, Hydroxysuccinimide- or NHS-ester), but TFP esters are less susceptible to spontaneous hydrolysis during conjugation reactions. TFP esters are stable for several hours at the basic pH, far outlasting succinimidyl esters.".
- Tetrafluorophenyl_esters wikiPageID "27743874".
- Tetrafluorophenyl_esters wikiPageLength "515".
- Tetrafluorophenyl_esters wikiPageOutDegree "3".
- Tetrafluorophenyl_esters wikiPageRevisionID "402256985".
- Tetrafluorophenyl_esters wikiPageWikiLink Category:Esters.
- Tetrafluorophenyl_esters wikiPageWikiLink N-Hydroxysuccinimide.
- Tetrafluorophenyl_esters wikiPageWikiLink Pentafluorophenyl_esters.
- Tetrafluorophenyl_esters wikiPageWikiLinkText "tetrafluorophenyl esters".
- Tetrafluorophenyl_esters hasPhotoCollection Tetrafluorophenyl_esters.
- Tetrafluorophenyl_esters subject Category:Esters.
- Tetrafluorophenyl_esters type Group.
- Tetrafluorophenyl_esters type Ester.
- Tetrafluorophenyl_esters type Group.
- Tetrafluorophenyl_esters comment "Tetrafluorophenyl (TFP) esters chemistry typically used to attach fluorophores or haptens to the primary amines of biomolecules. They produce as strong amide bound than succinimidyl esters (SE, Hydroxysuccinimide- or NHS-ester), but TFP esters are less susceptible to spontaneous hydrolysis during conjugation reactions. TFP esters are stable for several hours at the basic pH, far outlasting succinimidyl esters.".
- Tetrafluorophenyl_esters label "Tetrafluorophenyl esters".
- Tetrafluorophenyl_esters sameAs m.0cc82f0.
- Tetrafluorophenyl_esters sameAs Q7706346.
- Tetrafluorophenyl_esters sameAs Q7706346.
- Tetrafluorophenyl_esters wasDerivedFrom Tetrafluorophenyl_esters?oldid=402256985.
- Tetrafluorophenyl_esters isPrimaryTopicOf Tetrafluorophenyl_esters.