Method of detecting apolipoprotein E gene type and kit
An apolipoprotein and kit technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve problems such as high cost, low efficiency, complex technology, etc., achieve good detection stability, ensure reliability, High specificity and accuracy
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0080] Embodiment 1: Preparation of sample target nucleic acid
[0081] Draw 1ml of the subject's venous blood with a sterile syringe, add it to an anticoagulant tube containing EDTA, and store it at room temperature or at low temperature. Take 300 μl of anticoagulated whole blood and add it to a 1.5ml centrifuge tube, add 1ml of sterilized pure water to the centrifuge tube, mix well, and let stand at room temperature for 2-4 minutes. Then centrifuge (5000 rpm) for 6 minutes to collect the precipitate. After repeating the above steps once, add 1ml of normal saline to the centrifuge tube and mix well, centrifuge at 10000rpm for 10 minutes, and collect the white precipitate at the bottom of the tube. Add 50 μl of DNA extraction solution to the precipitate, mix thoroughly, bathe in boiling water for 10 minutes and centrifuge at 12000 rpm for 10 minutes. Take 2 μl of the supernatant as a template for the PCR reaction.
Embodiment 2
[0082] Embodiment 2: PCR amplification of target nucleic acid
[0083] Take several tubes of single-tube single-person PCR reaction solution, add 1 μl UDG enzyme to each tube, and then directly add 2 μl template (or negative and positive standards), mix well, and centrifuge instantaneously (3 seconds), put each reaction tube into the PCR machine After pretreatment at 50°C for 3 minutes, hot-start combined with "drop-down PCR" was used to amplify according to the following conditions: 4 minutes at 94°C, 3 minutes at 80°C, and 1 μl of Taq enzyme was added during this process. 94°C for 2 minutes for denaturation, then 94°C for 1 minute, 70°C for 1 minute, 72°C for 1 minute, a total of 5 cycles, and then press 94°C for 1 minute, 64°C for 1 minute, 72°C for 1 minute, a total of 30 cycles, A final 72°C extension was performed for 7 minutes. The amplified product was detected by 2% agarose gel electrophoresis (see Figure 2).
Embodiment 3
[0084] Example 3: Sample reverse dot blot detection of six known genotypes
[0085] Before hybridization, hybridization solution I (2×SSC-0.1% SDS) was mixed with hybridization solution II and preheated to 59°C for use. According to the number of samples to be tested, take six 1.5ml centrifuge tubes, add 0.5ml hybridization solution I to each tube and preheat to 59°C. After the PCR amplification product was denatured at 97°C for 5 minutes, it was placed in an ice-water mixture for 2-5 minutes. Then take 1000 μl hybridization solution I+2 μl solution I (1000:2) mixed solution as the binding solution and store it at 4°C for later use, and take the mixture of solution II: solution III: solution IV (1900:200:1) (19ml solution II+2ml Solution III + 10 μl solution IV) was used as a chromogenic solution protected from light for later use.
[0086] Before hybridization, fill the reaction chamber with distilled water, place the metal perforated plate, and turn on the water pump to dr...
PUM
Login to view more Abstract
Description
Claims
Application Information
Login to view more - 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.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap