Fusion protein of active group of hepatocyte growth factor receptor
A technology of hepatocyte growth factor and active group, applied in the field of DNA, can solve the problem of no obvious improvement in lung cancer patients, and achieve the effect of reducing autoimmune reactions
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Embodiment 1
[0040] (Example 1, Gene Sequence and Preparation of SMI-Fc Fusion Protein)
[0041] The structure of the SMI-Fc fusion protein constructed in this example is shown in figure 2 (a). The SMI-Fc fusion protein is fused with human immunoglobulin hIgG1-Fc by a functional group composed of Sema protein active group, MRS protein active group and IPT protein active group connected end to end.
[0042] The SMI-Fc fusion protein gene is obtained by amplifying the gene fragments of the above-mentioned Sema protein active group, MRS protein active group, IPT protein active group and hIgG1-Fc through polymerase chain reaction (PCR).
[0043] When performing PCR amplification, PCR primers cMet1F and cMet2RL and cMet nucleic acid template (nucleotide sequence sees SEQ ID NO.14), PCR primers cMet2FL and hIgGFcRev1 and human immunoglobulin heavy chain nucleic acid template (nucleotide sequence sees SEQ ID NO.14) NO.11) First perform the first PCR amplification respectively to obtain two PCR...
Embodiment 2
[0051] (Example 2, Gene Sequence and Preparation of SM-Fc Fusion Protein)
[0052] The structure of the SM-Fc fusion protein constructed in this example is shown in figure 2 (b). The SM-Fc fusion protein is fused with human immunoglobulin hIgG1-Fc by combining the functional groups formed by the Sema protein active group of cMet and the MRS protein active group end-to-end.
[0053] The SM-Fc fusion protein gene is obtained by amplifying the gene fragments of the above-mentioned Sema protein active group, MRS protein active group and hIgG1-Fc through polymerase chain reaction (PCR).
[0054] When performing PCR amplification, PCR primers cMet1F and cMet3RL and cMet nucleic acid template (nucleotide sequence sees SEQ ID NO.14), PCR primers cMet3FL and hIgGFcRev1 and human immunoglobulin heavy chain nucleic acid template (nucleotide sequence sees SEQ ID NO.14) NO.11) Perform the first PCR amplification respectively to obtain two PCR products; then PCR primers cMet1F and hIgGFc...
Embodiment 3
[0058] (embodiment 3, SM 2 - Preparation of Fc fusion protein)
[0059] The SM constructed in this example 2 -Fc fusion protein structure see figure 2 (c). SM 2 - The Fc fusion protein is fused with human immunoglobulin hIgG1-Fc by fusing two groups of Sema protein active groups and MRS protein active groups of cMet connected end-to-end.
[0060] SM 2 - The Fc fusion protein gene is obtained by amplifying the gene fragments of the above-mentioned Sema protein active group, MRS protein active group and hIgG1-Fc through polymerase chain reaction (PCR).
[0061] When performing PCR amplification, PCR primers cMet1F and cMet4RL and cMet nucleic acid template (see SEQ ID NO.14 for the nucleotide sequence), PCR primers cMet4FL and cMet3RL and cMet nucleic acid template (see SEQ ID NO.14 for the nucleotide sequence), The PCR primers cMet3FL and hIgGFcRev1 and the human immunoglobulin heavy chain nucleic acid template (see SEQ ID NO.11 for the nucleotide sequence) were firstly ...
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