The application provides a construction of a
fluorescent protein labeled microtubulin and a
microtubule binding protein universal bivalent carrier, and the process is as follows: a first stage is to construct a GFP-alpha
tubulin carrier, and a second stage is to construct a GFP-alpha
tubulin-
mCherry universal bivalent co-expression carrier; in the second stage, 35S,
mCherry and NOS sequences are inserted into a KpnI
enzyme cutting site of a
multiple cloning site of the GFP-alpha
tubulin carrier constructed in the first stage, and a single
nucleic acid enzyme cutting site is inserted into the 5' end and the 3' end of the
mCherry sequence, respectively, and the single
nucleic acid enzyme cutting site is XbaI, KpnI / Acc65I and AscI sequences, respectively, so as to obtain the universal bivalent carrier. The universal bivalent carrier provided by the application can express two target genes simultaneously, has the fluorescent signals of GFP and mCherry, can quickly and accurately identify a transgenic
plant, is convenient for positive
seedling screening, can be used for a tobacco transient expression experiment, can shorten an experimental period, and saves time and effort.