A kind of gene of transcription factor lcbhlh16421 of Liriodendron tulipifera and its application
A technology of lcbhlh16421 and transcription factors, applied in the field of plant genetic engineering, to achieve the effect of enhancing tolerance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] Example 1: Analysis of the bHLH family of Liriodendron tulipifera and the cloning of the LcbHLH16421 gene
[0030] Download the model plant Arabidopsis (https: / / www.arabidopsis.org) and rice (http: / / rapdb.dna.affrc.go.jp) databases to obtain bHLH family sequences, 177 and 135. Then use the protein domain alignment software HMMER3.0 to build a model to find out the potential bHLH family sequences of Liriodendron tulipifera, and then use BLASTP to compare the candidate bHLH family sequences of Liriodendron tulipifera. Through sequencing and homologous comparison, a sequence sequence homologous to bHLH transcription factor and highly similar to Lch16421 in Liriodendron tulipifera genome database was cloned, named LcbHLH16421 transcription factor.
[0031] 1. Extraction and quality detection of total RNA
[0032] Before extracting total RNA, all containers used in the extraction process need to be treated without RNase, in order to remove the interference of genomic DNA. ...
Embodiment 2
[0085] Example 2: Construction of Liriodendron LcbHLH16421 gene expression vector
[0086] 1. Design of enzyme digestion primers
[0087] According to the Pcambia2301 plasmid map ( image 3 ) and the characteristics of the LcbHLH16421 gene coding region, using the software Primer premier 5.0 to design the primers containing the restriction site for the ORF of the LcbHLH16421 gene. Search the ORF restriction site of LcbHLH16421 gene by software and find that there is no XbaI and BamHI restriction site in the LcbHLH16421 gene ORF, and the XbaI and BamHI double restriction primer can be designed as follows: LcbHLH16421-XbaI-F: 5′-GCtctagaATGGAAGAAGGAGCAGATG-3′ , LcbHLH16421-BamHI-R: 5'-CGggatccCTACATTGTCCCTTGGAAGC-3'.
[0088] 2. PCR amplification of the enzyme-cut fragment of the target gene
[0089] Same as "4, PCR amplification target gene sequence fragment" in Example 1
[0090] 3. Electrophoresis detection and recovery of amplified products
[0091] Same as "5. Electrop...
Embodiment 3
[0117] Example 3: Genetic transformation of Arabidopsis thaliana by the LcbHLH16421 gene mediated by Agrobacterium
[0118] 1. Freezing and thawing into Agrobacterium
[0119] (1) Melt Agrobacterium EHA105 competent cells on ice, add 2 μL of the extracted plant expression vector plasmid, and pipette the tip to mix;
[0120] (2) Ice bath for 30 minutes, freeze in liquid nitrogen for 1 minute, and then bathe in water at 37°C for 5 minutes;
[0121] (3) Add 700 μL LB liquid medium, shake at 28°C, 200 rpm for 3 hours;
[0122] (4) Centrifuge at 4000rpm for 3min, leaving a little supernatant;
[0123] (5) Mix the remaining bacterial liquid after transformation, and apply it on the LB solid medium containing Kan;
[0124] (6) Inverted culture at 28°C for 3 days
[0125] (7) Identification of positive clones.
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