Application of rice transcription factor Os05g39950 gene
A technology of n-linker-os05g39950, rice transcription factor, applied in the field of genetic engineering, can solve problems such as unseen OVATE protein regulation mechanism
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Embodiment 1
[0025] Example 1 Obtaining of Rice Transcription Factor Os05g39950 Gene and Construction of Plant Expression Vector
[0026] Log in to the http: / / rice.plantbiology.msu.edu / analyses_search_locus.shtml website, find the rice transcription factor Os05g39950 gene, and design PCR amplification primers based on its sequence:
[0027] Os05g39950-F: 5'-CAAAAAAGCAGGCTTCATGTTGTCCAGCGAACCAGG-3'
[0028] Os05g39950-R: 5'-CAAGAAAGCTGGGTCTGGCATGACGCCACAGG-3'
[0029] The leaves of rice 'Nipponbare' were used as materials, total RNA was extracted by TRIzol method, and cDNA was obtained by reverse transcription. The reaction steps were as follows: (1) Add the following substances sequentially on ice to a PCR reaction tube without nuclease: 6 μl of total RNA ( 0.1ng-5μg), Oligo(dT)18 primer 1μl, nuclease-free ddH 2 O 5 μl, placed in a PCR instrument at 65°C for 5 minutes; (2) Then add the following substances: 4 μl of 5× reaction buffer, 1 μl of RNase inhibitor, 2 μl of 10 mM dNTP, 1 μl of M...
Embodiment 2
[0032] The acquisition of embodiment 2 transgenic rice plants
[0033] Take the mature seeds of rice 'kitaake', shell them manually or mechanically, select the plump, smooth and spot-free seeds and inoculate them on the induction medium for induction culture after being sterilized. Rice callus with good appearance and good growth was selected as the recipient material, and ubi:Os05g39950-VP64 was transferred into the rice callus by the Agrobacterium-mediated method. The AAM transformation liquid of Agrobacterium was transformed, and the callus soaked in the transformation liquid was placed on the co-culture medium for co-cultivation, cultured in the dark at 25°C for 3 days, then placed on the screening medium for about 30 days, and subcultured every 10 days. Then, the screened out resistant calli were transferred to the differentiation medium for differentiation for about 20 days, and subcultured every 10 days. The resistant calli that differentiated into green seedlings were...
Embodiment 3
[0038] Example 3 Identification of Os05g39950-VP64 transgenic rice
[0039] In order to detect whether the CDS sequence of the Os05g39950 gene is integrated into the rice genomic DNA, the total DNA of wild-type and transgenic rice leaves was extracted by CTAB method, and the detection primer sequence was designed. The upstream primer: 5'-ATGGACGCGCTGGACGATTT-3', the downstream primer: 5 '-TCACTTGTCATCGTCGTCCTTGTAG-3', for PCR, the amplification system is: reaction buffer 5μl, dNTP 1μl, ddH 2 O 2.2 μl, Taq DNA polymerase 0.2 μl, upstream and downstream primers 0.3 μl, DNA template 1 μl. The reaction conditions were hot start at 96°C for 5 minutes; Extend for 10 minutes, and finally finish the reaction at 25°C. The transgenic plants were identified, and the amplified products were subjected to agarose gel electrophoresis. The electrophoresis results showed that the target bands were amplified in the transgenic rice, but the target band was not amplified in the wild-type rice ( ...
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