obr gene and its method for use as a genetic marker related to fat deposition in fat liver of Xupu goose
A genetic marker, Xupu goose technology, used in biochemical equipment and methods, determination/inspection of microorganisms, DNA/RNA fragments, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] Example 1 SNP screening of genes related to liver fat deposition in Xupu geese
[0048] 60 healthy Xupu geese of the same age were selected for feeding experiment. After 28 days for slaughter, Xupu goose livers were weighed and their genomic DNA was extracted from extreme samples (large and small livers).
[0049]According to the goose OBR gene sequence in GenBank, primers were designed with Primer 5.0, covering all exon 14 to exon 16 sequences of the gene. The primer sequences are: 5'-TTTGCCGTTAGTACCAGG-3' (forward), 5'-GCACAGACAAACAGGAGC- 3' (reverse), synthesized by Hunan Qingke Biotechnology Co., Ltd. The Xupu goose genomic DNA was amplified with the above primers.
[0050] PCR: 20 μl reaction system: 12 μl of 2×Master mix, 0.8 μl of upstream and downstream primers (10 μmol / L)), 1 μl of DNA template, and supplemented with ultrapure water to the required volume.
[0051] PCR amplification procedure: pre-denaturation at 95 °C for 5 min; denaturation at 95 °C for 30...
Embodiment 2
[0055] Example 2 Verification of SNPs related to liver fat deposition in Xupu goose in production practice
[0056] 14 healthy Xupu geese at 80 days of age and under the same feeding and management conditions were selected for the experiment. After 28 days of feeding, all the tested Xupu geese were slaughtered, and their livers were weighed.
[0057] 14 Xupu geese liver tissue-like genomic DNAs were extracted and amplified using the primers in Example 1, and their SNPs were detected according to the method in Example 1.
[0058] 1. PCR
[0059] The PCR reaction system is shown in the following table:
[0060] Table 1 PCR reaction system
[0061]
[0062] PCR cycling parameters are as follows:
[0063] Pre-denaturation at 95 °C for 5 min; denaturation at 95 °C for 30 s, annealing at 57 °C for 30 s, extension at 72 °C for 90 s, a total of 35 cycles; extension at 72 °C for 10 min, and final storage at 4 °C.
[0064] 2. Genotype frequency analysis of OBR gene SNP loci
[...
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