Pmon530
WebApr 27, 2024 · Then, the constructed vector and the pMON530 (used as the control) was transformed into the ASE strain and expressed in tobacco leaves, respectively. In the leaves of control vector transformed plant, the fluorescence of GFP was detected in the cytoplasm and nucleus (Figure Figure3 3). In contrast (to this), the fluorescence of SmWRKY1/GFP ... WebApr 25, 2000 · 35 S-AtNramp3 (filled bars): homozygous, single insertion line transformed with pMON530 containing AtNramp3 cDNA driven by the 35 S CaMV promoter. To determine whether AtNramp3 affects Fe accumulation, we measured the iron content of control and AtNramp3 overexpressing seedlings grown in minimal medium …
Pmon530
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WebMay 15, 2006 · This DNA fragment was cloned into a T-vector (TaKaRa, Japan), verified by sequencing, and inserted into the plant transformation vector pMON530 (Monsanto, USA), downstream to the 35S promoter. WebApr 22, 2024 · For construction of 35S pro:ERF109-GR, 35S pro:eGFP-ERF109 and 35S pro:ASA1, we inserted the ERF109 or ASA1 complementary DNA (cDNA) into the pMON530-GR, pMON530-eGFP or pMON530 vector.
WebMay 1, 2024 · The resultant pMON530:CaMV35S:TCD33-GFP plasmid was confirmed by sequencing and introduced into the Agrobacterium strain EHA105. The localization of TCD33 was investigated by transient expression assays of the GFP fusion protein in tobacco ( Nicotiana tabacum ) cells by laser scanning confocal microscopy (LSCM) as described … WebVector Database. Vector database is a digital collection of vector backbones assembled from publications and commercially available sources. This is a free resource for the scientific community that is compiled by Addgene. Only the plasmids deposited at Addgene are available for purchase through this website.
WebApr 9, 2015 · The pMON530:CaMV35S:ASL3-GFP plasmid was introduced into tobacco cells using Agrobacterium-mediated infection method. Meanwhile, empty GFP vector was used as a control. As a result, the green fluorescent signals of ASL3-GFP fusion protein perfectly overlapped with chloroplast autofluorescence in transformed tobacco mesophyll … WebJan 1, 1987 · The resultant plasmid, pMON530 (Fig. 7), retains the properties of pMON505 and the 35 S-NOS expression cassette now contains a unique cleavage site for Sinai between the pro- moter and polyadenylation signals. Tables listing the major restriction endonuclease cleavage sites useful for cloning and analysis of clones and transformants …
WebDec 1, 2016 · The authors are grateful to Prof. Zhongnan Yang (Shanghai Normal University) and Yaoguang Liu (State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, South China Agricultural University) for kindly providing pMON530-GFP vector, and the pYLgRNA-OsU6 and pYLCRISPR/Cas9-MH) vectors, …
WebJun 1, 2024 · The resultant pMON530-TCD11-GFP plasmids were introduced into tobacco (Nicotiana tabacum) leaves and co-cultured at 25 °C for 48 h. At the same time, the pMON530-GFP empty carrier was used as a control. pcl bg8502Webthe plasmid pMON530-GFP. Recombinant Agrobacterium tumefaciens strains.The recombinant plant expression vectors pMON337-TGMV-GFP and pMON530-GFP were introduced into Agrobacterium scrublet\\u0027 object has no attribute threshold_WebMar 21, 2016 · The resultant pMON530-TCM5-GFP plasmids were introduced into tobacco (Nicotiana tabacum) leaves and co-cultured at 25 °C for 2 days. At the same time, the pMON530-GFP empty carrier was used as a control. Then the GFP fluorescences in tobacco cells were observed using a Zeiss confocal laser scanning microscope ... scrubland vs shrublandWeb7.根据权利要求6所述一种采用草莓hy5基因调控草莓果实成熟周期的方法,其特征在于,所述过表达载体为pmon530-hy5。8.根据权利要求6所述一种采用草莓hy5基因调控草莓果实成熟周期的方法,其特征在于,所述宿主菌为农杆菌gv3101感受态。 pcl blowgunWebJan 1, 2024 · The full-length ORF of SmMYB1 (without the stop codon) was fused to a green fluorescent protein (GFP) gene under the control of the CaMV 35S promoter within a pMON530 vector to generate a SmMYB... scrublet downloadWebAug 25, 2016 · a pMON530-GFP, used as the blank vector control; b pMON530-SmDXS1-GFP; c pMON530-SmDXS2-GFP. Full size image. PCR and qRT-PCR analysis of transgenic hairy roots. The observed differential expression of the two SmDXS genes suggested that they perform distinct regulatory roles in the first step of the MEP pathway. scrublands habitatWebJan 1, 1987 · The resultant plasmid, pMON530 (Fig. 7), retains the properties of pMON505 and the 35 S-NOS expression cassette now contains a unique cleavage site for Sinai between the pro- moter and polyadenylation signals. p cl bond type