Recombinant oncolytic gene-adenovirus targeting cancer and construction method and application of recombinant oncolytic gene-adenovirus
An adenovirus and gene technology, applied in the field of recombinant oncolytic gene-adenovirus targeting cancer and its construction, can solve the problems of high harm to patients, inability to select tumor cells, and high side effects, and achieve good therapeutic effects and anti-cancer effects. Good effect, low toxicity effect
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Embodiment 1
[0063] The construction method of recombinant oncolytic gene-adenovirus Ad-sp-E1A-ΔE1B-VGLL4 targeting cancer is as follows: Step 1, construction of plasmid pCA13-VGLL4
[0064] (1) PCR method to obtain the VGLL4 gene fragment
[0065] Using the plasmid pcDNA-flag-VGLL4 as a template, the VGLL4 gene fragment was obtained by PCR.
[0066] The PCR reaction system is:
[0067]
[0068] The reaction procedure of PCR is:
[0069]
[0070] PCR products were run on 1% agarose gel electrophoresis. PCR results such as figure 1 shown. Among them, lane 1 is DNA Marker (Trans2K Plus DNA Marker); lane 2 is H 2 O (negative control); Lane 3 is the PCR product of pcDNA-flag-VGLL4.
[0071] The results showed that the target band was between 909bp and 750bp to 1000bp, indicating that the VGLL4 gene fragment was successfully amplified.
[0072] (2) Purification of PCR products
[0073] Purify the PCR product of the VGLL4 gene fragment obtained by PCR in Step 1 (1) with an agarose ...
Embodiment 2
[0142] Example 2 Identification of Recombinant Oncolytic Gene-Adenovirus Ad-sp-E1A-ΔE1B-VGLL4
[0143] (1) Extract viral genomic DNA according to the instructions of the blood genome extraction kit
[0144] (2) PCR identification of the VGLL4 gene carried by Ad-sp-E1A-ΔE1B-VGLL4 in step 4
[0145] The PCR reaction system is as follows:
[0146]
[0147] The reaction procedure of PCR is:
[0148]
[0149] Run electrophoresis after PCR. The result is as Figure 9 shown. Among them, lane 1 is DNA Marker (Trans2K Plus DNAMarker); lane 2 is the PCR product of Ad-sp-E1A-ΔE1B-VGLL4.
[0150] The results showed that the target band was 891bp, slightly below 1000bp, which proved that VGLL4 was amplified successfully.
[0151] (3) PCR to identify whether there is wild virus of E1A wild-type promoter recombinant type in the recombinant oncolytic gene-adenovirus Ad-sp-E1A-ΔE1B-VGLL4 obtained in Step 4 construction.
[0152] The PCR reaction system is as follows:
[0153] ...
Embodiment 3
[0163] Example 3 Titer determination of recombinant oncolytic gene-adenovirus Ad-sp-E1A-ΔE1B-VGLL4
[0164] The principle of virus titer determination is to determine the number of virus with infectious activity by counting the number of hexon-positive cells by immunocytochemical method, and measure the titer of the adenovirus after small amplification and purification according to the instructions on the adenovirus titer kit. .
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