Macaca fascicularis P450 2C18 medical metabolic enzyme and co-expression recombinant carrier with macaca fascicularis P450 oxidoreductase
A recombinant vector, technology of cynomolgus monkey, applied in the field of genetic engineering research
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Embodiment 1
[0018] Example 1. Cloning of cynomolgus monkey drug metabolizing enzyme P450 2C18 gene (cyp 2C18)
[0019] According to the published human P450 2C18 gene sequence (Genebank, Accession NO.: NM_000772), the following primers were designed:
[0020] Primer 1: 5'-AATGGATCCAGCTGTGG-3'
[0021] Primer 2: 5'-ATCTGCTCTTCTTCAGAC-3'
[0022] Using cDNA reverse transcribed from cynomolgus monkey liver RNA as a template, the coding region sequence (cyp 2C18) of cynomolgus monkey P450 2C18 was amplified by polymerase chain reaction (PCR), and the amplified PCR product was compatible with pMD 18- The T vector was ligated to obtain the pT-cynoP2C18 plasmid. Among them, the designed primers do not contain the coding region sequence (cyp 2C18) of cynomolgus monkey P450 2C18 except the initiation codon (ATG). After sequencing, the obtained coding region sequence has a full length of 1473 base pairs, encoding 491 amino acids. figure 1 It is the RT-PCR result map of cynomolgus monkey P450 2C...
Embodiment 2
[0023] Example 2. Construction and expression of cynomolgus monkey drug metabolizing enzyme P450 2C18 insect expression system
[0024] Using the above cloned cynomolgus monkey P450 2C18 gene (cyp 2C18) as a template, design primers containing RsrII and XhoI restriction endonuclease sites:
[0025] Primer 3: 5'-TTGCGGTCCGAATGGATCCAGCTGTGG-3'
[0026] Primer 4: 5'-CTTCTCGAGATCTGCTCTTCTTCAGAC-3'
[0027] The coding region sequence of cynomolgus monkey P450 2C18 (cyp 2C18) was amplified by PCR and inserted between the RsrII and XhoI restriction sites of the insect expression vector pFastBac-Dual to obtain the pFB-cynoP2C18 expression vector. Sequencing to confirm that the gene is correctly inserted into the vector.
[0028]The cynomolgus monkey P450 2C18 protein was expressed in sf-9 insect cells according to the operation manual of baculovirus expression. Briefly, the pFB-cynoP2C18 plasmid constructed above was used to transfect DH10Bac competent cells, positive clones were i...
Embodiment 3
[0029] Example 3. Cloning of cynomolgus monkey NADPH-cytochrome P450 oxidoreductase gene
[0030] According to the published human NADPH-cytochrome P450 oxidoreductase gene sequence (Genebank, Accession NO.: NM_000941), the following primers (primer 5 and primer 6) were designed:
[0031] Primer 5: 5'-ATGATCAACATGGGAGACTCCC-3'
[0032] Primer 6: 5'-CTAGCTCCACACGTCCAGGG-3'
[0033] Using the cDNA reverse transcribed from cynomolgus monkey liver RNA as a template, the coding region sequence of the cynomolgus monkey NADPH-cytochrome P450 oxidoreductase gene was amplified by polymerase chain reaction (PCR). The obtained PCR product was ligated with pMD 18-T vector to obtain pT-cynoPOR plasmid. After sequencing, the obtained coding region sequence has a full length of 2034 base pairs, encoding 677 amino acids. Figure 4 It is the RT-PCR result map of cynomolgus monkey P450 oxidoreductase, Lane 1: Marker DL2000 (the band sizes from top to bottom are: 2000bp, 1000bp, 750bp, 500bp,...
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