PEG modified nucleic acid aptamer as well as preparation method and application thereof
A nucleic acid aptamer and reaction technology, applied in biochemical equipment and methods, medical preparations containing active ingredients, pharmaceutical formulations, etc., to achieve good stability
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Embodiment 1
[0040] 1) Combine PEG5000, 0.400M 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (also known as EDC·HCl) and 0.100M N-hydroxysuccinimide The (NHS) molar ratio was 4:4:1 (50 μL each) after mixing, and shaking at 80 rpm for 15 min.
[0041] 2) Add FT6 aptamer with a volume ratio of 1:30 to PEG to 50μL of 2-(N-morpholine)ethanesulfonic acid buffer (also known as MES buffer) with a pH of 6 and then add it to Step 1) The prepared mixture was shaken at 80 rpm for 4 hours, and gel electrophoresis was performed after the reaction was completed.
Embodiment 2
[0043] 1) Combine PEG5000, 0.400M 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (also known as EDC·HCl) and 0.100M N-hydroxysuccinimide The (NHS) molar ratio is 5:5:1 (50 μL each) after mixing, and the reaction is shaken at 80 rpm for 10 min.
[0044] 2) Add FT7 aptamer with a volume ratio of 1:10 to PEG to 50μL of 2-(N-morpholine) ethanesulfonic acid buffer (also known as MES buffer) with a concentration of 20ml / L and a pH of 4 Solution), then add to the mixed solution prepared in step 1), shake for 2h at a rotation speed of 60 rpm, and perform gel electrophoresis detection after the reaction.
Embodiment 3
[0046] A PEG-modified nucleic acid aptamer preparation method, the steps are as follows:
[0047] 1) Combine PEG5000, 0.400M 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (also known as EDC·HCl) and 0.100M N-hydroxysuccinimide The (NHS) molar ratio is 2:2:1 (50 μL each) after mixing, and shaking at 100 rpm for 20 min.
[0048] 2) Add FT8 aptamer with a volume ratio of 1:50 to PEG to 50μL of 2-(N-morpholine)ethanesulfonic acid buffer (also known as MES buffer) with a pH of 7 and then add it to Step 1) The prepared mixture was shaken at 80 rpm for 5 hours, and gel electrophoresis detection was performed after the reaction.
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