SSR primer SSR81 used for identifying purity of hybrid seeds of Xiaguan No.1 zucchinis and identification method
A technology for hybrid seed purity and identification method, which is applied in the field of hybrid seed purity identification, can solve the problems of hybrid seed impurity, untimely emasculation, biological mixing, etc., and achieve the effects of short identification period, simple operation and low cost
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Embodiment 1
[0035] The screening process of the SSR primer SSR81 for the purity identification of Xiaguan No. 1 Zucchini hybrid seeds provided in this example is as follows:
[0036] Several pairs of primers designed according to the sequencing results of the wax gourd transcriptome were screened between the parents (Xiaguan No. The primer SSR81 with the band, the marker band pattern is clear and reproducible, and the sequence is as follows:
[0037] SSR81-F: 5'-GACAGAATTGGGGGTTTGTG-3' (SEQ ID NO.1);
[0038] SSR81-R: 5'-TCAACAGCAGTTGGTGGAAG-3' (SEQ ID NO. 2).
[0039] Using zucchini genomic DNA as a template, use the above SSR primer SSR81 for PCR amplification—PAGE for polyacrylamide gel electrophoresis of the amplified product—recover DNA from specific fragments (polyacrylamide non-denaturing gel)—PCR amplification—agarose Gel recovery—after TA clone sequencing, the analysis results showed that the primer SSR81 can produce a 181bp maternal specific marker SSR81 181 and the 188bp pat...
Embodiment 2
[0041] The method for identifying the purity of Xiaguan No. 1 Zucchini hybrid seeds provided in this example comprises the following steps:
[0042] (1) Genomic DNA extracted from the cotyledons of Chickpea
[0043] The experimental materials are "Xiaguan No. 1" Chinese zucchini hybrid experimental species and its male parent (Xiaguan No. 1 male parent) and female parent (Xiaguan No. 1 female parent) cotyledons. The steps for extracting cotyledon DNA are as follows:
[0044] ①Put a piece of cotyledon into a 2mL centrifuge tube, add liquid nitrogen and grind it with a grinding pestle, quickly add 800 μL 2% CTAB extract when the liquid nitrogen is quickly evaporated to dryness, mix well and place in a 65°C water bath for 45 minutes (shake well once every 10 minutes) );
[0045] ② After standing at room temperature, add 800 μL of chloroform:isoamyl alcohol (24:1), mix gently, let stand for 2 minutes, centrifuge at 12000 rpm for 15 minutes, transfer the supernatant (about 510 μL) t...
Embodiment 3
[0063] The method of Example 2 is used to plant and sample the Xiaguan No. 1 Chinese gourd hybrid that needs to be identified for its purity. There are 294 samples in total, and the individual plants are numbered sequentially, and the DNA of the individual plants is extracted for detection (see Figure 2-9 ), test results: 213 hybrid seeds, 81 female parents, seed purity of 72.45%, consistent with field test results.
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