Rapid detection method and kit for human Streptococcus pneumoniae based on magnetic separation and quantum dot labeling
A Streptococcus pneumoniae and quantum dot technology, applied in the field of medical testing, can solve the problems that cannot be used as a clinical diagnosis method, high quality requirements, false positives, etc.
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Embodiment 1
[0090] Example 1 Preparation of rabbit and mouse anti-human Streptococcus pneumoniae Fam1 PspA, Fam2 PspA protein polyclonal antibody IgG
[0091] (1) Preparation and purification of recombinant PspA1-His and PspA2-His fusion proteins
[0092] 1. Cloning of related genes
[0093]Bioinformatics analysis was performed on the Fam1 PspA and Fam2 PspA proteins of human Streptococcus pneumoniae (the accession numbers in the NCBI protein database are AAF27703 and AAF27712), respectively, to obtain the peptides with the most abundant antigenic epitopes in their extracellular domains, and to find their Corresponding DNA coding sequence, the whole gene sequence was chemically synthesized respectively after introducing restriction site NdeI at the 5' end, termination signal TAA and restriction site XhoI at the 3' end (full sequence synthesis was handed over to GenScript Biotechnology Co., Ltd. The company completed the delivery, and the artificially synthesized gene fragments were conne...
Embodiment 2
[0106] Example 2 Preparation of anti-human Streptococcus pneumoniae immune nano-magnetic beads
[0107] 1. Optimization of reaction conditions for anti-human Streptococcus pneumoniae Fam1 PspA protein polyclonal antibody coupled to magnetic beads:
[0108] Using magnetic beads coupled with rabbit anti-human Streptococcus pneumoniae Fam1 PspA protein polyclonal antibody IgG as the solid phase carrier, quantum dot-labeled mouse anti-human Streptococcus pneumoniae PspA protein polyclonal antibody as the detection antibody, through the principle of double antibody sandwich method The human Streptococcus pneumoniae subtype strain Sp6B antigen was detected, and the coupling between the magnetic beads and the polyclonal antibody was observed. A series of optimization options were carried out on the particle size of the magnetic beads, as well as the concentration of EDC / NHS activator, the concentration of conjugated antibody, the coupling time, and the type of blocking agent.
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Embodiment 3
[0123] Example 3 Preparation of quantum dot-labeled anti-human Streptococcus pneumoniae nanoprobe
[0124] 1. Optimization of IgG reaction conditions for nano carboxy quantum dot-labeled mouse anti-human Streptococcus pneumoniae Fam1 PspA protein polyclonal antibody IgG:
[0125] 1.1. Determination of the optimal labeling pH of the carboxyl quantum dot-labeled antibody probe
[0126] The pH of the phosphate buffer in the labeling reaction was set to 5, 6, 7, 8, and 9 respectively, and the fluorescence intensity of the labeled product was measured with a full spectrometer, and the influence of different pH values on the coupling reaction was observed, and the quantum dot labeled polyclonal antibody was determined. The optimum pH for the reaction is 7.0-8.0. This experiment chooses pH7.4.
[0127] 1.2. Determination of the optimal labeling amount of carboxy quantum dot-labeled antibody probes
[0128] Set the ratio of quantum dot molar concentration to polyclonal antibody c...
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