The use of baicalin combined with Atractylodes polysaccharides to up-regulate Treg cells in the treatment of immune recurrent abortion
A technique for treating Atractylodes polysaccharides and cells, which is applied in the field of medicine
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Embodiment 1
[0058] Example 1: Detection of the dose-effect relationship between baicalin and Atractylodes macrocephala polysaccharide, such as Figure 9 As shown, (1) Separation of mouse spleen cells followed by red blood cell lysis, removal of adherent cells, magnetic bead sorting of CD4+ T cells; (2) addition of anti-CD3 and anti-CD28 co-stimulatory factors as a blank control group, the experiment On the basis of adding anti-CD3 and anti-CD28, different concentrations of baicalin and Atractylodes polysaccharide were added to induce the differentiation of mouse Treg cells; (3) The concentrations of baicalin were 5 μM, 10 μM, 20 μM and 40 μM; The concentrations were 50 μg / ml, 100 μg / ml, and 200 μg / ml; (4) The proportion of Treg cells in each group of cells was detected by flow cytometry, and a curve was drawn to obtain the dose-effect relationship diagram of baicalin and Atractylodes macrocephala polysaccharide. The experimental results show that: the concentration of baicalin between 5 μ...
Embodiment 2
[0059] Example 2: Baicalin and Atractylodes polysaccharides respectively and jointly promote the flow detection of Treg cells, such as Figure 10 As shown, (1) Preparation of cells for detection: CD4+ T cells sorted by magnetic beads were spread in 24-well plates with 106 cells per well, and different concentrations of Atractylodes polysaccharide RAMP and baicalin were added to each group and combined administration , the cells can be collected after 72 hours for subsequent flow detection; (2) flow antibody staining: centrifuge at 400g for 5 minutes at 4°C, collect the cell pellet and medium supernatant respectively, wash the cell pellet with 1mL pre-cooled PBS buffer 2 times. Add 100 μL of anti-mCD16 / 32 blocking working solution to each tube of cells, incubate in an ice bath in the dark for 20 minutes, and add 1 mL of pre-cooled PBS buffer to wash the cell pellet twice. Add 2 μL FITC anti-mouse CD4 flow cytometry antibody and 5 μL APC anti-mouse CD4 flow cytometry antibody t...
Embodiment 3
[0060] Example 3: Atractylodes polysaccharides and baicalin respectively and jointly promote the qPCR detection of Treg cells, such as Figure 11 Shown, (1) the extraction of RNA: according to Qiangen company's The Plus Mini Kit instructions were used to extract total RNA; (2) RNA reverse transcription: according to Novizan’s The instructions of II Q RT SuperMix for qPCR kit guide to complete the reverse transcription of RNA; (3) Fluorescent real-time quantitative PCR: 1) The fluorescent real-time quantitative PCR (Quantitative real-time PCR, qPCR) primers used in this experiment were provided by Nanjing GenScript Company Synthesis. Centrifuge the synthesized dry powder of primers to make the primers gather at the bottom of the EP tube. Add nuclease-free water to dissolve the primers according to the instructions given by the company, and dilute the concentrated primer stock solution to a concentration of 2uM for use.
[0061]2) Each group needs to set up 3 duplicate wel...
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