A fluorescent probe for detecting butyrylcholinesterase activity and its preparation method and application
A butyrylcholinesterase and fluorescent probe technology, applied in the field of fluorescent probes, can solve problems such as no public detection function
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Embodiment 1
[0044] Two, 2,3-dicyano-1,4-phenylene diacrylate (DCPDA) to the fluorescence response of sulfhydryl compounds.
[0055] DCPDA, butyrylthiocholine and HEPES buffer. Apply the above fluorescence detection kit to butyrylcholinester
[0058] Except adding GSH at a concentration of 10.0 μM, 20.0 μM, 30.0 μM or 100.0 μM before adding 1.0 mM BTh,
[0061] In order to verify the function of BChE detection inhibitor screening, take tacrine as an example. Inhibition of BChE activity by tacrine
Embodiment 2
[0078] DCPDMA, butyrylthiocholine and HEPES buffer. Apply the above fluorescence detection kit to butyrylcholinester
[0079] First prepare a stock solution of DCPDMA solution in THF, wherein the DCPDMA solution is 10.0 mM; then mix 30.0 L
[0081] In addition to adding an amount of GSH (10.0 μM, 20.0 μM, 30.0 μM or 100.0 μM) prior to the addition of BTCh (1.0 mM)
[0082] The selective detection of BChE from mixtures with AChE was carried out as follows: containing specific levels of different species
[0083] In order to verify the function of BChE detection inhibitor screening, take tacrine as an example. Inhibition of BChE activity by tacrine
Embodiment 3
[0090] To 3.0 [mu]L of HEPES buffer was added 90 [mu]L of a 10.0 mM solution of DCPDFC. dissolved in the above DCPDFC
[0091] First prepare a stock solution of DCPDFC solution in THF, wherein the DCPDFC solution is 10.0 mM; then mix 30.0 μL
[0092] The experiment of the effect of GSH on the BChE assay was as follows: except that a certain
[0095] In order to verify the function of BChE detection inhibitor screening, take tacrine as an example. Inhibition of BChE activity by tacrine
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