Application of KDSR gene to preparation of deagnostic tool for myocardial infarction
A myocardial infarction and tool technology, applied in the application field of the product, can solve the problem of unclear expression of related genes, and achieve the effect of early diagnosis, better genetic diagnosis, and timely genetic diagnosis.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] Example 1 Screening of genes differentially expressed in patients with myocardial infarction and normal people
[0035] 1. Research object
[0036] Select 6 hospitalized patients with myocardial infarction treated in the hospital as research objects, including 3 males and 3 females, with an average age of 56.00±8.75; 7 healthy people in the control group; each of the above-mentioned patients and healthy people who were invited to participate in the study All signed the informed consent.
[0037] 2. Sample collection and storage
[0038] On the day of admission, 8 mL of fresh sterile arterial blood was collected into EDTA anticoagulated purple tubes before coronary angiography. If it is not used immediately, the sample can be stored in a refrigerator at 4°C for 2 hours.
[0039] 3. Separation of PBMCs by Ficoll method
[0040] The following steps are all completed in the ultra-clean bench:
[0041] (1) Dilute the blood sample with equal volume of normal saline, add ...
Embodiment 2
[0063] Embodiment 2QPCR experiment verifies the genes differentially expressed in patients with myocardial infarction and normal people
[0064] 1. Research object:
[0065] The screening criteria were the same as in Example 1, 35 patients with myocardial infarction and 35 normal subjects.
[0066] 2. Extraction of total RNA in blood
[0067] Step is with embodiment 1.
[0068] 3. RT-PCR
[0069] (1)RT
[0070] RT reaction system (20μl):
[0071]
[0072]
[0073] RT reaction procedure:
[0074] 42°C 15min
[0075] 85℃ 5s
[0076] 4℃ ---
[0077] (2) qPCR
[0078] PCR reaction system (20μl):
[0079]
[0080] PCR reaction program:
[0081] Amplification procedure:
[0082] Stage 1 95°C 10min
[0083] Stage 2 95°C 10s
[0084] 60°C 10s
[0085] Repeat 40 cycles
[0086] Three replicate wells were set for each sample, and the internal reference was GAPDH.
[0087] (3) Primers
[0088] The primer sequences of KDSR gene and GAPDH gene are as follows:
[0...
Embodiment 3
[0102] Example 3 Western blot experiment to verify the expression products of differentially expressed genes in patients with myocardial infarction and normal people
[0103] 1. Research object: same as embodiment 2.
[0104] 2. Mononuclear cell isolation
[0105] Take 10ml of venous blood from patients with myocardial infarction and normal people, inject it into a sterile vial containing heparin, and shake it gently immediately after capping. Add an equal volume of HBSS (NaCl 8.0g, NaCl 2 HPO 4 0.132g, KH 2 PO 4 0.06g, KCl0.4g, phenol red 1ml, NaHCO 3 0.35g, D-glucose 1.0g, dissolved in 1000ml double distilled water), to reduce the aggregation of red blood cells. Draw 8ml of lymphocyte stratification solution into a 50ml centrifuge tube, slowly add the diluted blood along the tube wall, keep the interface clear, do not mix the two, centrifuge at 20°C 2000r / min for 30min, carefully absorb the stratification solution and plasma transfer The turbid off-white layer, that i...
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