Recombination cell line and method for determining titer of baculovirus
A technology of recombinant cell line and baculovirus, applied in the biological field, can solve the problems of difficult to judge the nucleus, inaccurate results of virus titer determination, and enlargement of the nucleus.
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Embodiment 1
[0021] In an embodiment of the present invention, a method for constructing a recombinant cell line for baculovirus titer determination is provided, comprising the following steps:
[0022] Construction of reporter plasmids;
[0023] Wherein, the reporter plasmid includes a reporter gene encoding green fluorescent protein inserted therein, a promoter P gene of the late gene of the baculovirus that induces the expression of the reporter gene;
[0024] Using the reporter plasmid to transfect Sf9 insect cells;
[0025] Selecting the transfected Sf9 insect cells with a medium containing bleomycin and fetal bovine serum to obtain single cell clones;
[0026] The single cell clone is further screened with a medium containing bleomycin to obtain a recombinant cell line.
[0027] The recombinant cell line used for the determination of baculovirus titer provided by the embodiment of the present invention, which integrates the reporter gene capable of encoding green fluorescent protei...
Embodiment 2
[0032] Please refer to figure 1 , the construction method of this embodiment includes the following steps:
[0033] Step 101: constructing a reporter plasmid;
[0034] Since baculovirus gene expression is a sequential process, baculovirus genes can be divided into early genes and late genes according to the sequence of expression time. Considering the requirement of the promoter on the timing and expression quantity of the reporter gene expression, it is preferable to use the baculovirus very late gene containing the polyhedrin gene promoter P gene to regulate the expression of the reporter gene in the process of designing the reporter plasmid.
[0035] Specifically, the construction of the reporter plasmid can be obtained by the following methods:
[0036] 1. Starting from the transient expression vector plasmid pIZ / V5-His (Invitrogen, Life Science), use restriction endonucleases BsmI and SpeI to digest and recover a 2248bp band to obtain the vector framework pIZ / V5.
[00...
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