Application method, detection and treatment preparation of long chain non-coding rna LOC107987064
A RNALOC107987064, long-chain non-coding technology, applied in the field of molecular biology, can solve the problems of insufficient responsiveness of platinum-based chemotherapy regimens and no major breakthroughs, and achieve far-reaching practical significance and promotion effect.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0091] Detection Kit for LncRNA LOC107987064 in Tumor Tissues from Human Ovarian Cancer Patients
[0092] 1. Isopropanol 100ml
[0093] 2. Trizol reagent 100ml
[0094] 3. Chloroform 50ml
[0095] 4. 1μM random reverse transcription primer 50μl
[0096] 5. Enzyme-free water 2ml
[0097] 6. 10mM dNTP 100μl
[0098] 7. 200U / μl RNA reverse transcriptase 50μl
[0099] 8. 5× reverse transcription buffer 1ml
[0100] 9. 40U / μl RNase inhibitor 500μl
[0101] 10.Premix Ex Taq 50μl
[0102] 11. 10μM lncRNA LOC107987064 specific primer 50μl
[0103] Specific primers for fluorescent quantitative PCR:
[0104] lncRNA LOC107987064 forward primer: 5'-TCAGTGAGGGCCCCAGTTAG-3'
[0105] lncRNA LOC107987064 reverse primer: 5'-CTTTCAAGCTGGACAGAGCAT-3'
[0106] 12. 50 μl each of 10 μM internal reference and control primers
[0107] Specific primers for internal reference β-actin:
[0108] 5'-CCTATCGAGCATGGAGTGGT-3'
[0109] 5'-CTGAGGCATAGAGGGACAGC-3'
[0110] Specific primers for in...
Embodiment 2
[0115] In the previous research work, the applicant collected 8 tumor tissue samples from platinum-resistant and platinum-sensitive ovarian cancer patients, extracted total RNA from each tumor tissue sample, and performed real-time fluorescent quantitative PCR to analyze the expression of LncRNALOC107987064 after reverse transcription, and found that: The expression of LncRNA LOC107987064 was higher in tumor tissues of platinum-resistant patients than in platinum-sensitive patients (see image 3), and has a statistical difference, which is also consistent with the trend of high-throughput sequencing in the previous period. Accordingly, the applicant proposed to use LncRNA LOC107987064 to prepare a marker detection reagent for platinum resistance in human ovarian cancer. According to the results of repeated detection of LOC107987064 expression in platinum-resistant and platinum-sensitive patient tissues by qPCR experiments, we concluded that when the internal reference Actin cyc...
Embodiment 3
[0117] Detection of LncRNA LOC107987064 in Human Ovarian Cancer Cells and Induced Ovarian Cancer Platinum-Resistant Cells
[0118] (1) Collect human ovarian cancer parental cells and induced platinum-resistant ovarian cancer cells, and extract total RNA: Remove the culture medium in the culture plate, add 1ml Trizol, and place it horizontally at room temperature for 5 minutes, so that the lysate is evenly distributed in the Cell surface, then blow the cells with a pipette gun to make the cells fall off; transfer the cell lysate to a centrifuge tube, add 200μl chloroform, close the cap of the centrifuge tube tightly, shake up and down for 15 seconds, let stand on ice for 5 minutes, 12000g , centrifuge at 4°C for 15 minutes. Take out the centrifuge tube, the sample is divided into three layers: the light-colored supernatant aqueous phase, the middle white layer and the pink lower organic phase. Carefully absorb the light-colored supernatant and transfer it to another centrifuge...
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