Cancer-testis genetic marker related to primary lung cancer auxiliary diagnosis and application thereof
An auxiliary diagnosis and marker technology, applied in the fields of genetic engineering and tumor medicine
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0068] The collection of embodiment 1 sample and the arrangement of sample data
[0069] The inventor collected a large number of primary lung cancer blood samples from the Affiliated Cancer Hospital of Nanjing Medical University and the First Affiliated Hospital of Nanjing Medical University from April 2005 to January 2011. After sorting out the sample data, the inventor selected 5,408 samples from Whole Genome Microarray scans and individual Sequenom MassARRAY genotyped experimental samples meeting the following criteria:
[0070] 1. Selection of research samples
[0071] (1) Clinically diagnosed as primary lung cancer;
[0072] (2) Healthy controls matched with the age and gender of the case;
[0073] The demographic data and clinical data of these samples were collected systematically.
Embodiment 2
[0074] Whole Genome Scanning of SNP in Example 2 Peripheral Blood DNA
[0075] Among the 2,331 primary lung cancer patients and 3,077 healthy controls who met the above criteria, the two groups were matched in age and gender. The two groups of people were detected by Affymetrix 6.0 chip to obtain relevant results. The specific steps are:
[0076] 1. Add hemolysis reagent (i.e. lysate, 40 parts) to the leukocytes stored in the 2ml cryopreservation tube. The volume of the solution was adjusted to 2000ml, the same below), and it was completely transferred after inverting and mixing.
[0077] 2. Removal of red blood cells: Fill the 5ml centrifuge tube to 4ml with hemolysis reagent, mix by inverting, centrifuge at 4000rpm for 10 minutes, and discard the supernatant. Add 4ml of hemolysis reagent to the precipitate, invert and wash once again, centrifuge at 4000rpm for 10 minutes, and discard the supernatant.
[0078] 3. Extract DNA: add 1ml extract solution to the precipitate (e...
Embodiment 3
[0087] Example 3 Sequenom MassARRAY genotyping of a single SNP
[0088] The SNPs found to be associated with the onset of primary lung cancer in the above genome-wide scan were detected in another 1,500 cases of primary lung cancer and 3,000 healthy controls. The specific steps are as follows:
[0089] 1. Add the hemolysis reagent to the leukocytes stored in the 2ml cryopreservation tube, mix it upside down and transfer it completely.
[0090] 2. Removal of red blood cells: Fill the 5ml centrifuge tube to 4ml with hemolysis reagent, mix by inverting, centrifuge at 4000rpm for 10 minutes, and discard the supernatant. Add 4ml of hemolysis reagent to the precipitate, invert and wash once again, centrifuge at 4000rpm for 10 minutes, and discard the supernatant.
[0091] 3. Extract DNA: Add 1ml of extract solution and 8μl of proteinase K to the precipitate, shake and mix well on a shaker, and place in a water bath at 37°C overnight.
[0092] 4. Remove protein: add 1ml of saturate...
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