Molecular marker and application of common wheat low-molecular-weight glutelin Glu-B3h gene
A wheat and gene technology, applied in the biological field, can solve problems such as large number and small molecular weight
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Embodiment 1
[0045] Embodiment 1, the method for identifying whether Glu-B3h gene is contained in the wheat variety
[0046] 1. DNA extraction
[0047] Genomic DNA of common wheat leaves was extracted by CTAB method and ddH 2 O dissolves the extracted genomic DNA, and conducts quality inspection through 1% agarose gel electrophoresis. It is required that the extracted genomic DNA has no obvious impurities, clear bands, and no degradation.
[0048] 2. PCR amplification
[0049] Using the genomic DNA obtained in the above step 1 as a template, the molecular markers Glu-B3hF and Glu-B3hR in Table 1 were used for PCR amplification to obtain PCR amplification products.
[0050] Table 1. Molecular markers used to identify allelic variation of wheat Glu-B3h gene
[0051]
[0052] The PCR system is: about 100 ng of template DNA, 0.5 μL of TaqPlus enzyme (Tiangen Biochemical Technology Co., Ltd., ET105), 25 μL of GCbuffer II (Takara, DRR20GCI), 3 μL of dNTP (Takara, D4030RA), upstream and dow...
Embodiment 2
[0061] Embodiment 2, the application of molecular marker
[0062] 1. Application of molecular markers in identifying whether the wheat to be tested contains Glu-B3h gene
[0063] 1. Detect 28 materials with different low molecular weight glutenin (LMW-GS) compositions (material number 1-1~1 in table 2) with the method for identifying whether Glu-B3h gene is contained in the wheat variety to be tested in embodiment 1 -28) contains the Glu-B3h gene to verify whether the molecular markers in Example 1 are correct.
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