Application of long non-coding RNA LINC00842 as a biomarker in the preparation of prognostic detection preparations for lung adenocarcinoma
A long-chain non-coding, lung adenocarcinoma technology, applied in the field of tumor molecular biology, can solve the problems of being unable to adapt to the prognosis of lung adenocarcinoma patients, and having no reference standards and no specific indicators for the prognosis of lung adenocarcinoma patients. Achieve far-reaching clinical significance and promotional effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0013] Example 1 Preparation of long-chain non-coding RNA LINC00842 for lung adenocarcinoma prognosis detection kit (50 reactions)
[0014] 1. RNA stabilization solution 50ml
[0015] 2. Isopropanol 100ml
[0016] 3. Chloroform 100ml
[0017] 4. Trizol 50ml
[0018] 5. Enzyme-free water 10ml
[0019] 6.1μM random reverse transcription primer 50ul
[0020] 7. 5× reverse transcription buffer 200ml
[0021] 8. 10mM base triphosphate deoxyribonucleotides 100ul
[0022] 9. 40U / μl RNase inhibitor 500ul
[0023] 10. 200U / μl MMLV reverse transcriptase 50ul
[0024] 11. Premix Ex Taq 50ul
[0025] 12. 10μM long non-coding RNA LINC00842 real-time fluorescence quantitative PCR specific primers:
[0026] Forward primer 5'-CTGCCCAGTTAAGGCACAACTCTC-3' (SEQ ID NO.2),
[0027] Reverse primer 5'-AGCGCTGCGGAGAGGCAGTCT-3' (SEQ ID NO.3),
[0028] 13. 10μM internal reference GAPDH specific primers for real-time fluorescence quantitative PCR:
[0029] The forward primer is 5'-GTGGATATTG...
Embodiment 2
[0031] Example 2 Detection of long non-coding RNA LINC00842 in lung adenocarcinoma tissue
[0032] 1. Preservation of lung adenocarcinoma tissue: collect the lung adenocarcinoma tissue to be tested and store it in a cryopreservation tube filled with RNA stabilization solution, and put it in a -80°C refrigerator for later use.
[0033] 2. Extraction of RNA in tissues: Take an appropriate amount of specimen, add liquid nitrogen to the mortar after baking at 180°C for 6-8 hours, grind the specimen, grind to powder, add 1ml Trizol mortar specimen to the mortar, and grind into After the liquid is in the centrifuge tube, add 200μl / ml chloroform to the centrifuge tube, shake it by hand for 15-30s, place it on ice for 5min, and centrifuge at 12000g at 4°C for 15min; carefully take the upper aqueous phase into a new centrifuge tube, add Mix with 0.5ml of pre-cooled isopropanol, put it in a refrigerator at -20°C for 20min, centrifuge at 12000g at 4°C for 10min; discard the supernatant, ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


