msCT-CTx fusion protein transgenic engineering strain
A technology of transgenic engineering and fusion protein, applied in the field of fusion protein transgenic engineering strains, can solve problems such as inconvenience for patients, achieve the effects of less psychological burden, eliminating pain, and quick recovery
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specific Embodiment approach 1
[0018] Specific embodiment 1: In this embodiment, the msCT-CTx fusion protein transgenic engineering strain is named Escherichia coli BL21 (DE3-msCT / CTx), and Escherichia coli BL21 (DE3-msCT / CTx) is prepared according to the following steps:
[0019] 1. Digest the plasmid vector pUC (msCT / CTx) containing the msCT-CTx fusion protein gene with BamH I and EcoRI to obtain the DNA fragment of the msCT-CTx fusion protein;
[0020] 2. Digest plasmid pGEX-6P-1 with BamHI and EcoRI;
[0021] 3. The DNA fragment of the msCT-CTx fusion protein was enzyme-ligated to the vector pGEX-6P-1 after double enzyme digestion, and then placed at 16°C for overnight connection to obtain the vector pGEX-msCT / CTx;
[0022] 4. Transform Escherichia coli BL21 (DE3) with vector pGEX-msCT / CTx, and select positive recombinants to obtain msCT-CTx fusion protein transgenic engineered bacteria Escherichia coli BL21 (DE3-msCT / CTx).
[0023] Step 4 of this embodiment transforms Escherichia coli BL21 (DE3) by el...
specific Embodiment approach 2
[0024] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that: in step 1, the plasmid vector pUC (msCT / CTx) digestion reaction system is
[0025]
[0026] Other steps and parameters are the same as those in the first embodiment.
specific Embodiment approach 3
[0027] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is: the enzyme digestion reaction system of plasmid pGEX-6P-1 in step three is
[0028]
[0029] Other steps and parameters are the same as those in Embodiment 1 or 2.
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Abstract
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