Biomacromolecule cracking device and detection system thereof
A biomacromolecule and cracking device technology, applied in the field of biomacromolecule cracking devices and detection systems thereof, can solve problems such as the inability to achieve uniform size and controllability of products, and achieve additional use costs, convenient operation methods, and high degradation efficiency. Effect
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Embodiment 1
[0079] The structure of the biomacromolecule detection system is as follows: figure 1 shown. The purified abalone polysaccharide was used as material for controlled fragmentation and ionization.
[0080] Abalone polysaccharide is a kind of marine animal polysaccharide, and its sugar content reaches more than 90% in the purified material after measurement. The abalone polysaccharide was dissolved in pure water to prepare a 5% aqueous solution, and 2 mL was injected into the quartz medium ionization chamber from the injection port. After that, set the input voltage 60, 70, 80, 90V for 5 minutes and input current 1A for the upper and lower electrodes; or set the input voltage for 60V and input current 1A for 3, 5 and 7 minutes for the upper and lower electrodes . After the ionization stops, a small amount of water can be replenished from the replenishment pipe to maintain the original volume. Then, the retractable heating electrode extends into the quartz medium ionization ch...
Embodiment 2
[0087] The structure of the biomacromolecule detection system is as follows: figure 1 shown. The purified sea cucumber glycoprotein complex was used as the material for controlled fragmentation and ionization.
[0088] Sea cucumber glycoprotein complex is a marine animal glycoprotein, mainly composed of polysaccharides and proteins. The sea cucumber glycoprotein complex was dissolved in pure water to prepare aqueous solutions with concentrations of 1mg / mL, 3mg / mL and 5mg / mL, and then the device was used for plasma degradation. The injection volume is 2mL, and it is injected into the quartz medium ionization chamber from the injection port. After that, the upper and lower electrodes are electrified and ionized for 6 minutes, and the input voltage is set to 60V, and the input current is 1A. After the ionization stops, the retractable heating electrode extends into the quartz medium ionization chamber to contact the sample solution, and heats at 95°C for 2 minutes, then stops. ...
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