http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109266643-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_98ff87faa2dbe4480c778d12da9bd42a
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2710-00021
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filingDate 2018-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fec65dcdb0918bd0e6480127787ed5ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da5e838f1ba8b140cb547abcabd19660
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publicationDate 2019-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109266643-A
titleOfInvention Infectious clone of nematode virus in grape berry and construction method thereof
abstract The invention discloses a nematode infective clone of grape berry and a construction method thereof. The infective cloning vector is a seamlessly cloned fragmented grape berry endogenous necrosis virus genome fragment ligated into the pCB301‐2x35S-HDV RZ NOS vector containing the double 35S promoter and the ribozyme HDV-RZ. obtain. The vector was transferred to Agrobacterium EHA105 competent cells by freeze-thaw method, and the infectivity was verified by inoculating western tobacco and grapes with Agrobacterium. The GINV infective clone constructed by the invention can stably and efficiently express in the Agrobacterium EHA105 strain, and can successfully infect western tobacco and grape hosts. The acquisition of GINV invasive clones makes GINV studies easy to operate at the DNA level, providing a powerful tool for subsequent research on the biological properties and pathogenicity of GINV.
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priorityDate 2018-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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