2results about How to "Rapid lysis" patented technology

This invention belongs to the field of fungal detection technology, specifically relating to a micro-platform for rapid electrolysis and highly sensitive electrochemical nucleic acid detection of Cryptococcus neoformans and its application. The micro-platform includes an integrated microfluidic chip, an external power supply, a sample introduction system, and / or an imaging system. The integrated microfluidic chip includes an electrolysis region, an electrochemical detection region, and an electrode array region. The electrolysis region includes multiple vertically arranged counter electrodes arranged in pairs, and multiple horizontally arranged hollow channels in a serpentine pattern, bonded to the electrode pairs above them. The connection point between every two electroporated channels is the electroporation lysis point. The electrochemical detection region consists of a working electrode, a reference electrode, and a counter electrode. The working electrode is modified with rGO / AuNPs nanomaterials and molecular probes.

The invention belongs to the technical field of polypeptide cracking, and discloses a polypeptide cracking system which comprises a 50L cylindrical cone type cracking reaction kettle, a 500L settling kettle, a 100L drying kettle, an alarm recording module, a user management module, a system information module and a logout module. And the 500L sedimentation kettle is a vertical container made of 316L outer material and 316L inner material coated with PFA (Polyfluoroalkoxy) stainless steel. According to the invention, the splitting work of a large amount of polypeptide can be completed in a short time, the experiment efficiency is obviously improved, the advanced computer control system is adopted, the rapid and accurate splitting of the polypeptide can be realized, the manual operation is reduced, the experiment precision and efficiency are improved, and the high-purity splitting product can be generated by the polypeptide splitting system by accurately controlling the splitting condition; the workload of subsequent purification and separation is reduced, the polypeptide cracking system has good repeatability, the stability and consistency of each experiment result can be ensured, and the reliability and accuracy of the experiment are improved.