Method for predicating milk yield of small tailed han sheep by virtue of BMPR (bone morphogenetic protein receptor )-1B or PRLR (prolactin receptor) gene SNP (single nucleotide polymorphism) lotus
A technology for small-tailed Han sheep and milk production, applied in the field of animal husbandry, can solve problems such as inability to predict the future or newly born livestock, time-consuming and labor-intensive, etc., achieve good application prospects, improve survival rate, improve survival rate and development speed Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] Embodiment 1: BMPR-1B gene A746G site detection method
[0022] 1. Sample Collection and DNA Extraction
[0023] Blood was collected from the jugular vein of Small-tailed Han sheep, 2-5mL / sheep, anticoagulated with sodium heparin, and frozen at -20°C. Genomic DNA was extracted by phenol-chloroform extraction, dissolved in ultrapure water, and stored at 4°C until use.
[0024] 2. Primer sequence
[0025] According to the sequence of the sheep bone morphogenetic protein receptor IB (bone morphogenetic protein receptor IB, BMPR-IB) gene (GenBank accession numbers AF357007 and AF298885) containing the A746G mutation site, primers were designed, the amplification length was 140bp, and the primer sequence was:
[0026] Forward: 5'-GTCGCTATGGGGAAGTTTGGATG-3';
[0027] Reverse: 5'-CAAGATGTTTTCATGCCTCATCAACACGGTC-3'.
[0028] 3.PCR-RFLP
[0029] PCR 20μl reaction system composition: Taq DNA polymerase (5u / μl) 0.12μl; 10×PCR buffer 2μl; MgCl2 (25mmol / L) 2μl; dNTP (2.5mmol / L)...
Embodiment 2
[0034] Embodiment 2, PRLR gene E2-C34T site detection method
[0035] 1. Sample Collection and DNA Extraction
[0036] Blood was collected from the jugular vein of Small-tailed Han sheep, the blood sample was 2-5mL / sheep, anticoagulated with heparin sodium, -20. C frozen. Genomic DNA was extracted by phenol-chloroform extraction, dissolved in ultrapure water, and stored at 4°C until use.
[0037] 2. E2-C34T mutation site sequencing primer sequence
[0038] Primers were designed according to the second exon sequence of the sheep prolactin receptor gene PRLR, and the primer sequences were:
[0039] Forward: 5'-GACGTTTCTCTCCACCACAGAT-3'
[0040] Reverse: 5'-CCAACACACACGTGCTCAGA-3'
[0041] The length of the PCR product was 270bp, and the PCR product was sent to Shanghai Sangon Biological Co., Ltd. for sequence determination. Determine the SNP site according to the sequencing map.
[0042] 3. Determine the sequencing results based on the sequencing map, see figure 1 .
Embodiment 3
[0043] Example 3, BMPR-1B gene and PRLR gene SNP site and lactation volume correlation analysis
[0044] 1. Determination of lactation volume of Small Tail Han sheep
[0045] Under the same feeding conditions in the same sheep farm, 48 small-tailed Han sheep were sampled and measured once a week after lambing, and the continuous measurement was 8 times for 2 months. During the measurement, the ewes and lambs were separated for 24 hours. The milk was milked and isolated at 20.00 pm the night before, and three milkings were performed at 8.00 am, 14.00 noon, and 20.00 pm the next day, and were weighed and recorded. The three times were combined as the ewe’s lactation volume for one day, and the milk was weighed and fed back to the ewe. lamb.
[0046] 2. Correlation analysis between BMPR-1B gene A746G locus and lactation volume
[0047] Using SPSS13.0 statistical analysis software, the least square variance analysis was used to analyze the correlation between individuals with di...
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