Brassicatournefortii gouan fatty acid elongase and coding gene thereof
A fatty acid elongase, encoding gene technology, applied in the fields of molecular biology and genetic engineering, can solve the problem of complex erucic acid content
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] Embodiment 1, the cloning of gene BtFAE1
[0017] To clone BtFAE1, the specific steps are as follows:
[0018] 1. Acquisition of BtFAE1 gene
[0019] African mustard is cultivated under normal conditions. After the true leaves grow, the leaves are collected, DNA is extracted from the leaves, polymerase chain reaction is carried out, and the BtFAE1 gene is finally obtained.
[0020] 1. Extraction of African mustard genomic DNA
[0021] Take about 0.2g of fresh young living plant leaves, fully grind them under liquid nitrogen freezing conditions, transfer them to a 1.5mL centrifuge tube, add 500μL CTAB extract, and bathe in water at 65°C for 45min, during which time they are inverted and mixed 3 times; add 500μL volume Chloroform-isoamyl alcohol with a ratio of 24:1, mixed evenly, 12000r·min -1 Centrifuge for 15 min; take the supernatant, add 2 times the volume of absolute ethanol, and put it in the refrigerator at -20°C overnight; 4000r min -1 Centrifuge for 15min to...
Embodiment 2
[0031] Example 2, Functional Verification of BtFAE1 Gene
[0032] 1. High expression of BtFAE1 gene in yeast
[0033] In order to demonstrate the coding function of the BtFAE1 gene, the present invention clones the BtFAE1 gene between the BamHI and KpnI sites of pYES2 / NT C from Invitrogen, and transforms the yeast strain InvSc1 to obtain high-level expression.
[0034] The present invention utilizes the multiple cloning sites of the pYES2 / NT C high-efficiency expression vector of Invitrogen Company to realize the high-efficiency expression of BtFAE1. The enzyme cleavage site used in this experiment makes the 5' end of the product expressed by the pYES2 / NT C expression vector add 6 consecutive His fusion proteins, and these 6 consecutive His constitute the specific binding site of i-NTA gel. Therefore, the expression product can be purified by affinity chromatography.
[0035] The pMD-BtFAE1 recombinant vector carrying the BtFAE1 gene and the pYES2 / NT C expression vector were...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | aaaaa | aaaaa |
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