WebApr 13, 2024 · The KanMX6 fragment was amplified from the pFA6a-GFP(S65T)-kanMX6 plasmid. S. cerevisiae BY4741 competent cells were transformed with the amplified KanMX6 fragment using yeast transformation kit. Transformants were plated on YPD agar plates containing 600 ng/mL G418 and cultured at 30ºC for one week. Obtained colonies were … WebNov 10, 1998 · GFP-S65T and GFP-F64L/S65T (EGFP) were obtained from CLONTECH (Palo Alto, CA). The quadruple mutant F64L/Y66W/I167W/K238N (GFP-Y66W) was …
Green fluorescent protein retroviral vector : generation of high …
WebTwo mechanisms have been proposed: cyclisation-dehydration-oxidation (Mechanism A) and cyclisation-oxidation-dehydration (Mechanism B). To distinguish between these … WebGFP (S65T) and yeast ADH1 terminator Expression Mutation Promoter Availability Academic Institutions and Nonprofits only Enlarge pFA6a-GFP (S65T)-His3MX6 Plasmid #41598 Depositor John Pringle Article Longtine et al Yeast. 1998 Jul;14 (10):953-61. Insert His3 Use Yeast genomic targeting Tags A. gossypii translation elongation factor 1a gene… generally normally 違い
FlyBase Recombinant Construct Report: P{UAS-GFP.S65T}
WebApr 18, 2008 · The green fluorescence protein used in these plants is referred to as GFP S65T, a “red shifted” version of the original jellyfish GFP [14-16]. This GFP was engineered to have a peak excitation at 488 nm and peak fluorescence at 512 nm, and has been deployed widely in the laboratory environment as a reporter for plants [1, 17, 18]. WebGFP was also detected in individual living plant cells following transient transfection of soybean suspension cultures, demonstrating that GFP is an effective transformation marker in plant cells. Similarly, transient transfection of mammalian cells with a modified form of GFP, S65T, allowed detection of single living cells expressing the reporter. WebApr 13, 2024 · The oligonucleotide primers used for strain and plasmid construction in this study are listed in Table S1. A previously described recombinant polymerase chain reaction (PCR) method (Krawchuk and Wahls 1999) was used to construct the tfs1::kanMX6, mca1::kanMX6, moc3::kanMX6, tfs1-GFP(S65T)-natMX6, and tfs1-13Myc-natMX6 strains. dealertrack title