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Tetrafluorophenyl esters : ウィキペディア英語版 | Tetrafluorophenyl esters 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. ==See also==
*Pentafluorophenyl esters (PFP)
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Tetrafluorophenyl esters」の詳細全文を読む
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