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适配体的解链温度和退火问题,求大神解惑?

图一:sDNA和MB-rp的解链温度为67℃
            sDNA和APT的解链温度为79.7℃
图二:sDNA,MB-rp,OTA-APT三条适配体在90℃退火5min,形成如图三所示结构
图三:经退火后三条适配体形成的结构
图一图二图三均来自一篇文献,求助大家,退火温度已经超过了DNA的解链温度,适配体形成的链会不会被分解,还可以形成这样的结构吗?
下一个实验想要做类似的,真心求助哦,拜托大神解答一下呀


图一



图二



图三
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共2个回答
图一文字:Melting temperature (Tm) (sDNA to MB-rp)=67 ℃,Tm (sDNA to OTA-APT)= 79.7 ℃. Two Tm value were much
higher than reaction temperature, which indicated the hybridization of the selected DNA are stable in the process of the OTA detection.
图二文字:MB-rp (1 m M), sDNA (1 m M), and OTA aptamer (APT) (1 m M) were
annealed together at 90 ℃ for 5 min, followed by decreasing
gradually to room temperature to form stable hybrid structures
(sDNA/MB-rP/APT) as the ratiometric probe. The gold electrode
(GE) was polished to obtain a mirror surface using 0.3 and 0.05 m m
alumina powder in order and then the electrode was ultrasonic
cleaned byethanol and deionized water, respectively. Afterthat, the
electrode was electrochemically cleaned in H 2 SO 4 (0.5 M) by CV
scanning in the potential range of 0.2e1.6 V until a stable voltam-
metric peak obtained. Then drop sDNA/MB-rP/APT mix solution
(10 m L) on the surface of electrode for 1 h to form the sDNA/MB-rP/
APT/GE through the AueS interaction, and then the modified
electrode was immersed in MCH (1 mM) solution for 1h at room
temperature to block the unoccupied sites.
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