Biomarker for auxiliary diagnosis of recurrent abortion, and application thereof
A recurrent miscarriage, biomarker technology, applied in disease diagnosis, biological testing, biomaterial analysis, etc., can solve problems such as unclear pathogenesis, and achieve the effect of promoting migration, invasion and proliferation
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Embodiment 1
[0024] The expressions of FUT4 and α1,3 fucose were detected in the villi of normal women and patients with recurrent miscarriage, and the villi were processed by paraffin embedding.
[0025] 1. Detection of localization and expression of FUT4 and α1,3 fucose in villous tissue by immunohistofluorescence
[0026] (1) Dewaxing: Put the prepared paraffin sections into the following solutions in turn: soak in xylene I for 10 minutes, then soak in xylene II for 10 minutes, soak in 100% ethanol I for 5 minutes, soak in 100% ethanol II for 5 minutes, and soak in 95% ethanol Soak for 5 minutes, soak in 85% ethanol for 5 minutes, soak in 70% ethanol for 5 minutes; then rinse with slow water for 10 minutes, do not directly wash the slices. Dip in PBS 3 times, 5min each time.
[0027] (2) Antigen retrieval: Put the slices into citrate buffer, cover them, and thaw in a microwave oven for 20 minutes. Take it out and let it cool down to room temperature naturally.
[0028] (3) Rinse with...
Embodiment 2
[0054] 1. Immunofluorescence detection of FUT4 and α1,3 fucose expression in trophoblast cells of different experimental groups (Scramble control group, FUT4 siRNA transfection group, FUT4 siRNA and FUT4 cDNA transfection group simultaneously)
[0055] Slide: After the cells are digested with trypsin, centrifuge at 800 rpm for 4 minutes, resuspend in fresh medium, put the cell suspension into a petri dish with slide, and let the cells grow on the slide.
[0056] Collection: remove the culture medium in the culture dish, wash with PBS 3 times, 3 minutes each time.
[0057] Fixation: add 4% paraformaldehyde to the petri dish obliquely, and fix it for 20 minutes.
[0058] Paraformaldehyde was discarded, washed 3 times with PBS, 3 min each time.
[0059] Sealing: Select slides and place them in a wet box, add immunostaining blocking solution to seal for 1 hour.
[0060] Primary antibody incubation: clip the slices from the blocking solution, blot dry on filter paper, incubate wi...
Embodiment 3
[0067] In Vitro Migration Experiment of Early Pregnancy Villi Explants
[0068] (1) Laying gel: melt matrigel in a refrigerator at 4°C, dilute matrigel with serum-free medium DMEM / F-12 at a ratio of 1:2, gently blow and mix, add 50 μL to each well of a 96-well plate matrigel, try not to generate air bubbles, and place in a 37°C incubator.
[0069] (2) The villous tissue in the first trimester of pregnancy was obtained from healthy women undergoing artificial abortion in the obstetrics and gynecology operating room of the affiliated hospital for non-medical reasons, and the blood clots were rinsed with pre-cooled sterile PBS immediately.
[0070] (3) Put the villous tissue into a large dish containing PBS in a sterile operating table, and cut into 2-5mm fragments.
[0071] (4) Carefully transfer to the matrigel of the 96-well plate so that it is anchored in the center of the matrigel.
[0072] (5) After anchoring for 4-6 hours, add complete medium, observe the morphology unde...
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