Application of ARRDC2 in evaluating development process of oral squamous cell carcinoma
A technology for ARRDC2 and oral squamous cell carcinoma, applied in the field of biomedicine, can solve the problems of lack of quantitative indicators, affecting the objectivity, accuracy and repeatability of tumor grading, achieve individualized treatment, avoid insufficient treatment intensity, and avoid overtreatment Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Example 1 Screening Gene Markers Related to Oral Squamous Cell Carcinoma
[0043] 1. Sample collection
[0044] 68 oral squamous cell carcinoma tissues and adjacent tissues were collected, including 20 patients with histological grade I (G1), 30 patients with histological grade II (G2), and histological grade III (G3 / G4) patients in 18 cases. The patients did not receive any treatment before operation. All the above-mentioned samples were obtained with the consent of the organizational ethics committee, and 4 samples were taken from each group for detection and analysis of gene expression profiles, screening of differentially expressed genes, and verification experiments were carried out in all samples of each group.
[0045] 2. Preparation of RNA samples (operated using QIAGEN tissue RNA extraction kit)
[0046] Take out the tissue samples frozen in liquid nitrogen, put the tissue samples into a pre-cooled mortar for grinding, and extract and isolate RNA according t...
Embodiment 2
[0061] Example 2 QPCR sequencing to verify the differential expression of the ARRDC2 gene
[0062] 1. Large-sample QPCR verification of differential expression of ARRDC2 gene.
[0063] 2. The RNA extraction steps are as described in Example 1.
[0064] 3. Reverse transcription:
[0065] Use FastQμant cDNA First Strand Synthesis Kit (Product No.: KR106) for reverse transcription of mRNA, first remove the genomic DNA reaction, add 5×gDNA Bμffer 2.0μl, total RNA 1μg, add RNase Free ddH 2 O Make the total volume to 10μl, heat in a water bath at 42°C for 3min, then add 2.0μl of 10×Fast RT Bμffer, 1.0μl of RT Enzyme Mix, 2.0μl of FQ-RT Primer Mix, RNase Free ddH 2 O5.0 μl, after mixing, add to the above-mentioned test tube and mix together a total of 20 μl, heat at 42°C for 15 minutes in a water bath, and heat at 95°C for 3 minutes.
[0066] 4. QPCR amplification detection
[0067] QPCR amplification primers were designed according to the sequences of ARRDC2 and GAPDH, and synth...
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