Method for detecting and identifying variety of snake venom by utilizing adaptor technology
A technical detection and aptamer technology, applied in the field of biomedical testing, can solve the problems of finding species-specific monoclonal antibodies, blind treatment, and missing the best time for treatment, etc.
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Embodiment 1
[0032]A kind of Chinese cobra venom identification method based on aptamer technology, carries out as follows:
[0033] 1) Screening of genus-specific aptamers of Chinese cobra venom, constructing a random single-stranded DNA (ssDNA) library and primers, synthesizing the single-stranded DNA library into a double-stranded DNA library by PCR, and amplifying the DNA by asymmetric PCR Library, PCR amplification products were purified and recovered by phenol-chloroform method to obtain a large number of purified single-stranded DNA libraries.
[0034] 2) Screening cycle of Chinese cobra venom: Dialyze the Chinese cobra venom and coat it on the enzyme-linked plate, react at 37°C for 3 hours, and set a blank control well at the same time. Sample wells and control wells were blocked with 3% BSA for 2 hours. Put 1ng of the purified single-stranded DNA library in the SELEX binding buffer to react with the blank control well at 37°C for 40 minutes, reverse-screen to remove the single-st...
Embodiment 2
[0043] A method for identifying Agkistrodon venom based on aptamer technology, which is carried out as follows:
[0044] 1) Screening of species-specific aptamers for Agkistrodon venom, constructing a random single-stranded DNA (ssDNA) library and primers, synthesizing the single-stranded DNA library into a double-stranded DNA library by PCR, and then using asymmetric PCR to amplify DNA library, PCR amplification products are purified and recovered by phenol-chloroform method to obtain a large number of purified single-stranded DNA libraries.
[0045] 2) Screening cycle of Agkistrodon venom: After dialysis, the venom of Agkistrodon was coated on the enzyme-linked plate, and reacted at 37°C for 3 hours, and a blank control well was set at the same time. Sample wells and control wells were blocked with 3% BSA for 2 hours. 1 ng of the purified single-stranded DNA library was first reacted with the blank control wells at 37°C for 40 minutes in SELEX binding buffer, reverse-screen...
Embodiment 3
[0054] A method for identifying the venom of Agkistrodon halys in Jiangsu and Zhejiang based on the aptamer technology is carried out as follows:
[0055] 1) Screening of species-specific aptamers for Agkistrodon halys venom, constructing a random single-stranded DNA (ssDNA) library and primers, synthesizing a double-stranded DNA library from the single-stranded DNA library by PCR, and amplifying the DNA by asymmetric PCR Library, PCR amplification products were purified and recovered by phenol-chloroform method to obtain a large number of purified single-stranded DNA libraries.
[0056] 2), Jiangsu-Zhejiang Agkistrodon venom screening cycle: the Jiangsu-Zhejiang Agkistrodon venom was dialyzed and coated on an enzyme-linked plate, and reacted at 37°C for 3 hours, and a blank control well was set at the same time. Sample wells and control wells were blocked with 3% BSA for 2 hours. Put 1ng of the purified single-stranded DNA library in the SELEX binding buffer to react with th...
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