Sweet potato low-temperature-resistant related protein IbICE1 and coding genes and application thereof
A coding, protein technology, applied in the application, the use of vectors to introduce foreign genetic material, angiosperms/flowering plants, etc., can solve the problems of death, increased consumption, blocked energy production and material synthesis, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1、I
[0081] Embodiment 1, the acquisition of IbICE1 protein and its coding gene
[0082] 1. Extraction and purification of total RNA from leaves
[0083] About 2 g of the expanded leaves of Liaoshu 36 field seedlings were taken, ground into powder in liquid nitrogen, added to a 10 mL centrifuge tube, and the total RNA of sweet potato leaves was extracted with the Applygen Plant RNA Extraction Kit (Applygen Technologies Inc, Beijing).
[0084] mRNA was purified from total RNA using the QIAGEN ligotex Mini mRNA Kit (QIAGEN, GmbH, Germany). Take 1 μL of mRNA and check its integrity by electrophoresis on 1.2% agarose gel, and another 2 μL is diluted to 500 μL, and its quality (OD 260 ) and purity (OD 260 / OD 280), detected by non-denaturing agarose gel electrophoresis, the 28S and 18S bands were clear, and the brightness ratio of the two was 1.5-2:1, indicating that the total RNA was not degraded, and the purified mRNA met the experimental requirements and could be used for sweet po...
Embodiment 2
[0096] Embodiment 2, the acquisition of IbICE1 sweet potato plant and its low temperature resistance analysis
[0097] 1. Obtaining of sweet potato plants transfected with IbICE1
[0098] 1. Construction of recombinant vector pCAMBIA3301-IbICE1
[0099] (1) According to the coding sequence of the sweet potato IbICE1 protein cDNA, design and amplify the primer sequence of the complete coding sequence, the forward and reverse primers respectively introduce the BglII and PmlI restriction sites, and the primer sequences are as follows:
[0100] Primer 7: 5'- AGATCT ATGAACACACCAAGCCTAGCA-3' (the underlined part is the BglII restriction site);
[0101] Primer 8: 5'- CACGTG CTATACCAACCCATGGAAGGC-3' (the underlined part is the restriction site of PmlI).
[0102] (2) Using the DNA molecule shown in sequence 1 in the artificially synthesized sequence listing as a template (or using Liaoshu 36 cDNA as a template), PCR amplification was performed using primers 7 and 8 to obtain a PC...
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