Application of cotton GHPSAT2 gene in promoting flowering of plants
A gene and plant technology, applied in the application field of GHPSAT2 gene in promoting plant flowering, can solve problems such as few researches
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[0023] The following examples are used herein to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventors to be employed in the practice of the invention, and thus can be considered preferred modes for its practice. However, those skilled in the art should understand from this specification that many modifications can be made to the specific embodiments disclosed herein, and the same or similar results can still be obtained without departing from the spirit or scope of the present invention.
[0024] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art to which this invention belongs, and the disclosures cited herein and their cited materials are all incorporated by reference .
[0025] Those skilled in the art will recognize, or ...
Embodiment PBI121
[0035] The construction of embodiment PBI121-GhPSAT2 expression vector
[0036] 1 Obtain the gene sequence of GhPSAT2 (Gh_D07G1721) from CottonFGD, use Oligo 7 software to design primers, and use PCR method to amplify from upland cotton No. The molecular weight is 46.26213kDa, and the isoelectric point is 8.52.
[0037] Amplification primers are as follows:
[0038] Upstream primer F (SEQ ID No.1): 5'-ATGGCAGCAACATCTCTAAAT-3'
[0039] Downstream primer R (SEQ ID No.2): 5'-TCAAGCATGCTTTGCCTGGAA-3'
[0040] The open reading frame sequence is (SEQ ID No.3):
[0041]ATGGCAGCAACATCTCTAAATGCCCCTAACGCTCCTCTCCTTCAAAA GACCCATCAAACTCATGTCTTTCTCAAACCCATCTCCACCATTCCTTGTCA AACCTCTGCCAAGCGCTTCTCCATCTCTTGTTCCGCAACTACCCAAGATCG CCTCTCCGTCCAATCCCAATCTCAAGATCGGGTCTTTAACTTCGCCGCCGG TCCCGCCACCTTACCCGAGAACGTCCTCCTCAAAGCCCAATCCGAGCTTT ACAACTGGCACGGATCTGGCATGAGCGTTATGGAAATGAGCCACCGTGGT AAGGATTTCCGTTCTATTATCGAAAAAGCCGAGGCCGATCTCCGTTCTCTT CTCAACATCCCTGAAAACTACGCCGTTTTGTTCCTCCAAGGTGGAGCCAC CACCCAGTTC...
Embodiment 2
[0145] Transformation of Arabidopsis thaliana mediated by embodiment 2 Agrobacterium
[0146] Transformation of Arabidopsis thaliana by inflorescence dipping method
[0147] 1) Inoculate 20 μL of the Agrobacterium liquid cultured at -20°C into 1 mL of LB liquid medium, shake at 28°C and 180 rpm overnight, and take 200 μL of the activated bacteria liquid and add it to 50 mL of LB liquid medium at 28°C and shake at 180 rpm.
[0148] 2) OD of the bacteria solution 600 When the value is about 1.2, centrifuge at 5,000rpm for 5min to collect the bacteria.
[0149] 3) Discard the supernatant, and use 50-70ml transformation medium to reselect the bacterial solution to make the OD 600 Infection begins after the value is 0.8-1.0 (transformation medium formula: 0.217g 1 / 2MS, 5g sucrose, 100mL water dissolved, then add 20μL silwetL-77).
[0150]4) Select unflowered Arabidopsis thaliana, place the Arabidopsis inflorescences in the transformation medium for 30-50 seconds, place them hori...
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