Kit and method for detecting polymorphism of CYP2D6 gene
A gene polymorphism and kit technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of long time, long time, and complicated steps for CYP2D6 gene polymorphism, so as to save detection time. , high accuracy, and the effect of reducing pollution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0050] Embodiment 1. Preparation of kit
[0051] 1. Primer design for internal reference gene ACTB and CYP2D6 gene
[0052] According to the gene sequence, the internal reference gene ACTB sequence and the CYP2D6 gene sequence are derived from the National Center for Biotechnology Information Nucleic Acid Database (NCBI), wherein the internal reference gene ACTB ID is 60, and the reference sequence number is NG_007992.1. See also SEQ in the sequence list of the present invention ID NO: 15; CYP2D6 gene ID is 1565, and the reference sequence number is NG_008376.2. Primer5.0 primer design software was used to design specific primers for the internal reference gene ACTB and CYP2D6 gene, including: exon 1 to exon 9 of CYP2D6 gene The upstream and downstream primers of the full-length amplification specific primers of exons; the upstream and downstream primers of the first exon sequencing primers of CYP2D6 gene; the upstream and downstream primers of the second exon sequencing prime...
Embodiment 2
[0073] Example 2. Detection of CYP2D6 gene polymorphism with the kit prepared in Example 1
[0074] Take the results of random detection of peripheral blood samples from 30 subjects as an example.
[0075] The detection process of using the kit of the present invention to detect CYP2D6 gene polymorphism in the population is as follows: firstly, obtain the peripheral blood sample of the clinical subject, and quickly extract the genomic DNA; secondly, first prepare the PCR reaction solution of the internal reference gene ACTB, and then add the concentration Both 2ng / μl of the internal reference gene ACTB sequence and 2μl of the internal positive control sequence were amplified by PCR. After PCR, electrophoresis was performed on agarose DNA gel with a concentration of 2% to check the PCR amplification. If there are two bands of about 390bp and 800bp in the PCR amplification product of the internal reference gene ACTB, it indicates that the entire detection process is valid. If on...
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