LOC105376287 as a diagnostic and therapeutic molecular marker for osteoporosis
Through the detection and inhibition of LOC105376287, the accuracy problem of early diagnosis of male osteoporosis is solved, more efficient diagnosis and treatment effects are achieved, and the ability to identify and treat osteoporosis is improved.
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Examples
Embodiment 1
[0062] Example 1 Screening for Differentially Expressed Molecules
[0063] 1. Case collection
[0064] Five elderly male patients with osteoporosis were selected, aged 62-79 years; the diagnosis of osteoporosis was based on the standards established by the Osteoporosis Committee of the Chinese Society of Geriatrics, that is, the bone mineral density at the same site was lower than the peak value of the area and decreased by two standard deviations classified as osteoporosis. During the same period, 6 healthy elderly men (healthy control group) were selected, aged 61-78 years. The selected objects exclude diabetes, primary hyperparathyroidism, hyperthyroidism, hypercortisolism, liver and kidney dysfunction, alcoholism, malnutrition, rheumatoid arthritis and other diseases that affect bone metabolism; no application within half a year Androgens, calcitonin, large amounts of calcium, bisphosphonates, and other drugs that affect bone metabolism. The two groups were comparable i...
Embodiment 2
[0105] Example 2 Large sample verification screened out differentially expressed LncRNA
[0106] 1. Sample collection
[0107] According to the method of Example 1, 32 cases of osteoporosis patients and 30 cases of male healthy controls were collected.
[0108] 2. Extract blood total RNA
[0109] Step is with embodiment 1.
[0110] 3. Validation at the RNA level
[0111] (1) Reverse transcription: According to the measured RNA concentration, 1000 ng of RNA was quantified for each sample for reverse transcription. Use the DDR037A reverse transcription kit of Dalian Biobiology, add 20ul of the system (see Table 1), add it to a 200ul enzyme-free EP tube, centrifuge and put it into a PCR instrument, and set the temperature conditions as follows: 37°C for 15min, 85°C for 5sec . After the end, the cDNA was diluted 10 times and stored at -20°C for future use.
[0112] Table 1 Reverse transcription system
[0113]
[0114] (2) Real-time quantitative PCR
[0115] Shanghai Sa...
Embodiment 3
[0128] Example 3 Effect of LOC105376287 on proliferation and differentiation of osteoblasts
[0129] 1. Interference efficiency pre-test
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