http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007181417-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8233792a15cd19fc671cdfdaa1200087
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2006-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b2f52d2eb860fc56058af50919c5e03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66a0b4b825d9e2b598c3f01bc3ea0fda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cdc3119937103c95e36f744758ac6520
publicationDate 2007-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007181417-A
titleOfInvention Splicing analysis vector
abstract A versatile splicing analysis vector capable of easily detecting splicing abnormality of a specific gene fragment using a sample containing a gene (genomic DNA) and a splicing analysis method using the vector. A splicing analysis vector in which at least two normally functioning exon sequences and a sequence containing a multicloning site are arranged between the at least two exon sequences. The gene fragment that is the object of analysis is incorporated into the multi-cloning site of the two exon sequences on the vector, introduced into the cell, the gene is transcribed, and a mature mRNA is generated. It can be confirmed whether or not the derived substance is contained. [Selection] Figure 1
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114934058-A
priorityDate 2006-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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