Expression method of animal alpha interferon and gamma interferon
An expression method and alpha interferon technology, applied in the field of recombinant interferon preparation, can solve the problems of inability to form polyhedron, low expression efficiency, destruction of polyhedrin gene, etc., and achieve improved titer and stability, and reduced sensitivity. , the effect of high expression efficiency
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Embodiment 1
[0034] Example 1 Joint expression of porcine alpha interferon and gamma interferon
[0035] 1 Experimental method
[0036] Firstly, the sequences of porcine interferon-alpha and interferon-gamma should be obtained, and the codons in the wild-type porcine interferon sequence should be replaced with the preferred codons in the silkworm baculovirus after transformation, cloned and connected to the pVL1393 vector after synthesis, The two interferons are connected through the IRES sequence, and the recombinant shuttle plasmid for expressing the target protein can be obtained in the process of co-transfection with BmNPV DNA by means of homologous recombination.
[0037] 1.1. For the preparation of the solution and medium, please refer to the relevant literature (Joseph et al., Molecular Cloning Experiment Guide, Third Edition, 2002; Osper et al., Refined Molecular Biology Guide, 1998)
[0038] 1.2 Acquisition of porcine α-interferon, γ-interferon sequence and IRES sequence and tran...
Embodiment 2
[0125] Example 2 Co-expression of porcine alpha interferon (SIFNA) and gamma interferon (SIFNG)
[0126] 1 Experimental method
[0127] The co-expression loci of porcine interferon-alpha and interferon-gamma were the polyhedron gene locus (expressing SIFNA) and P10 gene locus (expressing SIFNG) on ReBm-dcc-d1629, respectively.
[0128] SIFNA is recombined into the baculovirus shuttle plasmid ReBm-dcc-d1629-d10 by means of the pVL1393 vector (the construction method of ReBm-dcc-d1629 has been published in CN102286534A (the title of the invention is: Insect bioreactor expressing multiple foreign genes and Its construction method and application) are disclosed in detail in the invention patent application documents, and its microbial preservation number is the polyhedron gene locus on CGMCC No.4914); the method of SIFNG recombination to the P10 gene locus is to rely on the EGFP marker gene through reverse The screening method was operated recombinantly in Escherichia coli.
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Embodiment 3
[0174] Example 3 Joint expression of canine alpha interferon and gamma interferon
[0175] 1 Experimental method
[0176] Firstly, the sequences of canine α-interferon (Canis lupus familiaris IFNA, abbreviated as CIFNA) and γ-interferon (Canis lupus familiaris IFNG, abbreviated as CIFNG) should be obtained, and the codons in the wild-type interferon sequence should be replaced by silkworm For the preferred codons in baculovirus, the two sequences are synthesized and then cloned and connected to the pVL1393 vector. The two interferons are connected through the IRES sequence, and can be co-transfected with BmNPV DNA by homologous recombination. The recombinant baculovirus obtained in the method was used to infect the silkworm to obtain the protein to be expressed.
[0177] 1.1 Sequence modification and synthesis of canine α-interferon and canine β-interferon
[0178] Refer to the literature on canine α-interferon and canine β-interferon reported at home and abroad in recent ye...
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