Molecular marker of TaGS2 gene related with wheat plant height, obtaining method and application thereof
A molecular marker and high-correlation technology, which is applied in biochemical equipment and methods, microbial measurement/inspection, DNA/RNA fragments, etc., can solve the problems of photosynthetic efficiency and yield reduction, poor ventilation and light transmission in the middle and lower parts, and easy lodging, etc. problems, to achieve the effect of improving selection efficiency and quality, fast and accurate screening, and improving quality and output
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0031] Embodiment 1 Relevant with wheat plant height TaGS2 Acquisition of molecular markers for genes
[0032] 1. Wheat Konon 9204 TaGS2 gene cloning
[0033] Design primers according to the results of database analysis:
[0034] Nucleotide sequence of upstream primer: 5'-TCCTCCCTCGTCTCGTCCGCGT-3' (SEQ ID NO: 3)
[0035] Nucleotide sequence of downstream primer: 5'-AGTGCCCCGACGGAACCACAGG-3' (SEQ ID NO: 4)
[0036] Total RNA was extracted from the three-leaf stage seedlings of hexaploid wheat Kenong 9204, and 1284bp full-length cDNAs of TaGS2-A, TaGS2-B and TaGS2-D coding genes were amplified by RT-PCR.
[0037] The specific operation process is as follows:
[0038] 1) Plant total RNA extraction: Grind 100 mg of wheat Konon 9204 seedlings with liquid nitrogen, transfer to an EP tube containing 1 mL of Trizol reagent after grinding, mix well, and let stand at room temperature for 5 min; add 0.2 mL of chloroform, fully Mix well and let stand at room temperature for 2-3 min;...
Embodiment 2
[0062] Example 2 Application of Molecular Marker IN10 in Detection and Screening of Wheat Varieties or Strains
[0063] (1) Use IN10 labeled primers (upstream primer nucleotide sequence such as SEQ ID NO: 1, downstream primer nucleotide sequence such as SEQ ID NO: 2) to F 6 The DNA of 188 derivative lines of the generation RIL population was amplified by PCR respectively. The PCR amplification system was 20 μl, including: 10 μl of 2×Taq PCR MasterMix, 1 μl of upstream and downstream primers, 1 μl of DNA template of the wheat to be tested, and the rest with ddH 2 O supplementation; PCR amplification program: pre-denaturation at 94°C for 5 min; denaturation at 94°C for 30 s, annealing at 56°C for 30 s, extension at 72°C for 1 min / kb, 30 cycles; extension at 72°C for 7 min; storage at 20°C ;
[0064] (2) Put the above amplification products on 6% non-denaturing polyacrylamide gel (6% non-denaturing polyacrylamide gel means that 100ml polyacrylamide gel solution contains 5.85 g ...
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