Application of miR-21 in preparation of medicine for treating intrauterine adhesion and/or thin inner membranes
A technology of intrauterine adhesions and mir-21, applied in the application field of medicine, can solve problems affecting endometrial fibrosis and other problems
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Embodiment 1
[0027] Example 1 Expression of miR-21 in endometrial tissues of patients with normal and severe intrauterine adhesions
[0028] 1. Materials, reagents, equipment
[0029] 1.1 Source of human endometrial tissue
[0030] Collect 5 cases of normal endometrial tissues and 5 cases of endometrial tissues from patients with severe intrauterine adhesion syndrome. When obtaining endometrial tissues, the size of follicles was detected by ultrasound to ensure that all the stages of endometrial tissue acquisition were unified into the late stage of proliferation. All participants signed a written informed consent form, which was approved by the Ethics Committee of Nanjing Drum Tower Hospital.
[0031] 1.2 Main reagents
[0032] MicroRNA in situ detection probe HAS Probe TM (Pengji Kaifeng Biotechnology Co., Ltd.), hybridization kit (Pengji Kaifeng Biotechnology Co., Ltd.), anti-digoxigenin antibody (Anti-Digoxigenin-AP, Roche), NBT / BCIP color development (Pengji Kaifeng Biotechnology C...
Embodiment 2
[0039] Example 2 Effect of miR-21 on fibrosis of endometrial epithelial cells
[0040] 1. Materials, reagents, equipment
[0041] 1.1 Main reagents
[0042] Collagenase (Sigma), Hyaluronidase (Sigma), DNAase (Roche), Epithelial Cell Culture Medium (Gibco), Serum (Gibco), Trizol (Invitrogen), Reverse Transcriptase (Takara), Qpcr Enzyme (Roche).
[0043] 1.2 Main instruments
[0044] Cell incubator, shaker, qPCR instrument (Roche), PCR instrument (ABI)
[0045] 1.3 Main method
[0046] 1.3.1 Isolation and culture of primary endometrial epithelial cells
[0047] Place the endometrial tissue in a new 60mm petri dish, cut the tissue until no lumps are visible to the naked eye, add the prepared digestive solution, blow and mix, and place it in a 37°C incubator for 5 minutes; take out the petri dish and observe the tissue under a microscope Digestion: Add DNase at a concentration of 4mg / mL, continue to digest for 5mim; pipette the digested tissue, and drop the tissue suspension in...
Embodiment 3
[0052] Example 3 miR-21 reverses Np63-induced endometrial epithelial cell fibrosis.
[0053] 1. Materials, reagents, equipment
[0054] 1.1 Main reagents
[0055] E-cadherin antibody (Abcam), N-cadherin antibody (Abcam), fluorescent secondary antibody (Jackson), dapi-containing mounting medium (Abcam), PFA, antibody diluent (Gibco), methanol, Tween, PBS.
[0056] 1.2 Main instruments
[0057] Fluorescence microscope (Leica), shaker
[0058] 1.3 Main method
[0059] The expression of E-cadherin and N-cadherin was detected by cell immunofluorescence. After the endometrial epithelial cells were sliced, the Np63 adenovirus infected the cells for 24 hours. After 48 hours of transfection with miR-21, the slides loaded with cells were taken out. Wash 3 times with 1×PBS, 5 min each time, then fix with PFA at room temperature for 15 min, wash 3 times with 1×PBS, 5 min each time. Treat the cells with pre-cooled methanol for 5 minutes, wash with 1×PBS 3 times, 5 minutes each time....
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