A carrier for in situ analysis of intracellular protein complexes and its preparation method and application
A technology for in situ analysis of protein complexes, applied in analytical materials, material separation, instruments, etc., can solve the problems of difficult in situ targeted analysis of intracellular protein complexes, strong cross-linking agent activity, and many side reactions, etc. Achieve the effect of solving the difficulty of in situ targeted analysis, low cytotoxicity, and excellent biocompatibility
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Embodiment 1
[0029] With 2 mass parts of castor oil polyoxyethylene ether, molecular weight is 15 mass parts of polylactide-glycolide of 10000, 1 mass part of didodecyl dimethyl ammonium bromide, crosslinking agent (disuccinimide Suberate) 4 mass parts are dissolved in the dichloromethane of 500 mass parts. The above mixture was poured into a 1% by mass polyvinyl alcohol aqueous solution, and ultrasonicated for 2 minutes, and the carrier was solidified with a 1% by mass polyvinyl alcohol aqueous solution after the ultrasonication was completed. The TEM photo of the carrier obtained in this embodiment is as follows figure 1 shown. The particle size and surface potential of the prepared materials are shown in Table 1.
[0030] Table 1. DLS test data (1, 2, 3 are three DLS tests for the carrier)
[0031] 1 2 3 Particle size / nm 274.6 268.8 273.7 PDI 0.237 0.181 0.135 Zeta potential / mv 38 39.9 41
[0032] Depend on figure 1 It can be seen from the T...
Embodiment 2
[0035]With castor oil polyoxyethylene ether 3 mass parts, molecular weight is 15 mass parts of polylactide-glycolide of 20000, didodecyl dimethyl ammonium bromide 1 mass part, crosslinking agent (disuccinimide Suberate) 5 mass parts are dissolved in the dichloromethane of 400 mass parts. The above mixture was poured into 1% polyvinyl alcohol aqueous solution, ultrasonicated, and the carrier was further solidified with 1% polyvinyl alcohol solution. The particle size of the prepared carrier is 126.6nm±0.75nm, and the potential (Z-potential: 46.6±0.379mv) meets the conditions for it to be used as a transmembrane transporter.
[0036] In the study of the in situ analysis of the cross-linking agent carrier for protein complexes, the carrier and the cells were co-incubated in 1640 culture medium. After incubation for 3 hours, the cells were collected, and then the proteins and protein complexes were extracted from the cells using ionic liquids. The extracted protein and protein co...
Embodiment 3
[0038] With 5 mass parts of castor oil polyoxyethylene ether, molecular weight is 15 mass parts of polylactide-glycolide of 80000, 2 mass parts of didodecyl dimethyl ammonium bromide, crosslinking agent (disuccinimide Suberate) 8 mass parts are dissolved in the dichloromethane of 700 mass parts. The above mixture was poured into 0.5% polyvinyl alcohol aqueous solution, ultrasonicated, and the carrier was further solidified with 2% polyvinyl alcohol solution. The particle size of the prepared carrier is 236.6nm±0.92nm, and the potential (Z-potential: 49±0.379mv) meets the conditions for it to be used as a transmembrane transporter.
[0039] In the study of the cross-linking agent carrier used in the in situ analysis of protein complexes, the carrier and cells were co-incubated in 1640 culture medium. After incubation for 6 hours, the cells were collected, and then the proteins and protein complexes were extracted from the cells using ionic liquids. The extracted protein and pr...
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