Mitochondria-related seminal plasma miRNAs taken as mankind severe asthenospermia markers, and applications thereof
A technology of asthenozoospermia and markers, applied in the fields of genetic engineering and reproductive medicine
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0081] Embodiment 1 Research Object Selection and Grouping Basis
[0082] The inventor collected semen samples from severe asthenospermia cases and normal fertile control adult males who met the requirements from July 2007 to October 2012 from the Reproductive Medicine Center of Nanjing Medical University. 80 cases of normal fertile controls (average age: 22.15±3.45 years old) and 80 cases of severe asthenospermia (average age: 22.32±3.51 years old) were used as experimental subjects for qRT-PCR detection of miRNA expression. Specific sample classification criteria are as follows:
[0083] (1) Repeat the semen quality test and be diagnosed with severe asthenozoospermia;
[0084] (2) Normal sexual function, excluding patients with known causes such as cryptorchidism, history of vascular trauma, orchitis, vas deferens obstruction, vasectomy, polychromosomal abnormalities, and Y chromosome azoospermia factor microdeletion
[0085] (3) Healthy male controls matched with the age ...
Embodiment 2
[0089] Example 2 Mitochondria-related miRNATaqManarray screening
[0090]Preparation of cDNA samples: a) Take 100 μl seminal plasma; b) Add 900 μl Trizol, shake and mix, centrifuge at 12,000 rpm for 15 minutes at 4°C, discard the waste liquid in the lower layer; c) Add 1.5 times the volume of supernatant ethanol, shake and mix, transfer to the spin column, centrifuge at 12000rpm for 15 seconds, and discard the lower layer of waste liquid; d) add 700 μl of RWT buffer to the spin column, centrifuge at 10000 rpm for 15 seconds, and discard the lower layer of waste liquid. e) Add 500 μl of RPE buffer to the spin column, centrifuge at 10,000 rpm for 15 seconds, and discard the lower layer. f) Repeat e. g) Add the spin column to a new 2ml tube and centrifuge at 10000rpm for 1 minute to remove the RPE buffer. h) Add 50 μl of DEPC-treated water to the column and centrifuge at 12000 rpm to collect RNA. i) Then cDNA is obtained by RNA reverse transcription reaction. The reverse tran...
Embodiment 3
[0100] Example 3 qRT-PCR method to measure the expression of mitochondria-related miRNA in seminal plasma
[0101] The primers (Table 1) were designed for the quantitative Real-time PCR detection of each miRNAs in the seminal plasma of 80 cases of normal fertility controls and 80 cases of severe asthenospermia.
[0102] (1) Preparation of cDNA samples: a) Take 100 μl of seminal plasma; b) Add 900 μl of Trizol, shake and mix, centrifuge at 12,000 rpm at 4°C for 15 minutes, discard the lower layer of waste liquid; c) add 1.5 times the volume of supernatant absolute ethanol, shake and mix Mix well, transfer to the spin column, centrifuge at 12000rpm for 15 seconds, discard the lower waste liquid; d) add 700 μl RWT buffer to the spin column, centrifuge at 10000 rpm for 15 seconds, discard the lower waste liquid. e) Add 500 μl of RPE buffer to the spin column, centrifuge at 10,000 rpm for 15 seconds, and discard the lower layer. f) Repeat e. g) Add the spin column to a new 2ml tu...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com