SSR marker primer set for identifying germplasm resource genetic relationship of halogeton glomeratus and application of SSR marker primer set
A technology for labeling primers and kinship relationships, applied in the field of plant biology, can solve the problems of germination characteristics, growth characteristics, salt enrichment characteristics of plants, differences in growth periods, and it is difficult to effectively distinguish the ecotypes of halophytes in different regions, and achieve stability. Good, abundant, high polymorphism effect
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Embodiment 1
[0043] This embodiment provides a set of SSR marker primers for identifying the genetic relationship of halophyte germplasm resources, including 33 pairs of primers with polymorphisms, and the primer sequences are shown in the sequence table SEQ ID 1 to SEQ ID 66 and the following table , the annealing temperature is 58-60 °C, and the number of repetitions is between 12-30.
[0044]
[0045]
Embodiment 2
[0047] This embodiment provides a method for identifying the kinship of halophyte germplasm resources using the SSR marker primer set described in Example 1, including the following main steps:
[0048] 1. DNA extraction. Take the sample to be identified, and use the seeds or seedlings to extract the total plant DNA.
[0049] 2. PCR amplification. Using the total DNA obtained in step (1) as a template, PCR amplification was carried out with the above-mentioned 33 pairs of SSR marker primer sets for identifying the genetic relationship of halophyte germplasm resources.
[0050] 3. Electrophoresis detection. The PCR amplification products were detected by denaturing polyacrylamide gel electrophoresis, and stable and clear PCR amplification products were obtained.
[0051] 4. Data statistics. The PCR amplification products obtained in step (3) are counted, and the SSR analysis results are recorded in binary and genotype. , 2, 3, etc. represent different genotypes.
[0052] ...
Embodiment 3
[0060] This example provides the application of the SSR marker primer set design method described in Example 1 and the identification of the affinity of halophyte germplasm resources, including:
[0061] 1. Sample collection and DNA extraction
[0062] Before and after December in winter, the seeds of different halophyte ecological types were collected from 18 sites in the arid area of central Gansu and Hexi Corridor (attached). figure 1 ), using the seeds or seedlings cultivated in flowerpots for 1 month as materials, using the CTAB method to extract the genomic DNA of halophyte, and using a micro-ultraviolet spectrophotometer to detect the DNA concentration and purity, the concentration is 300-500ug / mL, The absorbance value OD260 / OD280 is between 1.7-1.9.
[0063] 2. Screening of primers for SSR polymorphism
[0064] The SSR primers in the halophyte have not yet been developed, so the halophyte three-generation full-length transcriptome was sequenced (https: / / www.ncbi.nl...
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