Application of gene marker in diagnosing ischemic cardiomyopathy
A technology of ischemic cardiomyopathy and genes, applied in the field of biomedicine, can solve the problems of different incidence rates of coronary heart disease and CHD
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0071] Example 1 Screening for Gene Markers Related to Ischemic Cardiomyopathy
[0072] 1. Sample collection
[0073] 1) Collection of blood samples
[0074] Blood samples from 25 normal people and patients with ischemic cardiomyopathy were collected, and the EDTA anticoagulant tubes were allowed to stand for 10 minutes, then the serum was separated by centrifugation, and stored at -20°C for later use.
[0075] 2) Collection of tissue samples
[0076] Left ventricular tissue samples were collected from 25 patients with ischemic cardiomyopathy and from 10 non-cardiomyopathy deaths.
[0077] Inclusion criteria for patients with ischemic cardiomyopathy: refer to Burch's (1972) diagnostic criteria for ICM and the New York Heart Association (NYHA) cardiac function classification criteria to determine: (1) have a clear history of coronary heart disease (angina pectoris) , myocardial infarction more than half a year, electrocardiogram and enzyme abnormalities) evidence; (2) obviou...
Embodiment 2
[0090] Example 2 QPCR sequencing to verify the differential expression of TMEM30B gene
[0091] 1. According to the detection results of high-throughput sequencing, the TMEM30B gene was selected for large-sample QPCR verification.
[0092] 2. RNA extraction
[0093] Use QIAGEN's tissue RNA extraction kit to extract total RNA, and blood RNA extraction kit to extract blood RNA. For specific steps, refer to the instruction manual.
[0094] 3. Reverse transcription:
[0095] 1) Add dNTP mixture 1μl, Oligo dT primer 1μl, total RNA 2μg, add RNase FreeddH 2 O Make the total volume to 10 μl, carry out denaturation and annealing reaction on the PCR instrument, 65°C, 5min, place at 4°C after the reaction is completed.
[0096] 2) Construct a 20 μl reaction system, continue to add 4 μl of 5×Primer Script Buffer, 0.5 μl of RNase Inhibitor, 0.5 μl of Prime Script RTase, RNase Free ddH 2 O 5.0 μl, carry out the reverse transcription reaction on the PCR instrument according to the follow...
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