http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20060000838-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f875ead9da2c49fb9b91ec886b9354eb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6844
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2004-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e0d39596a5c012078691e2ae63816b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b884b867e24cb6b7b4a30d8f35d50cae
publicationDate 2006-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20060000838-A
titleOfInvention AML1-ETO Metering Kit
abstract The present invention provides PCR reaction mixtures, probe and primer mixtures capable of detecting AML1-ETO fusion genes, probe and primer mixtures capable of detecting ABL genes, AML1-ETO standard plasmid DNA, ABL standard plasmid DNA, AML1-ETO negative The present invention relates to a method for quantifying AML1-ETO fusion genes using a control kit and an AML1-ETO quantitative kit including an ABL negative control group and an electric kit. When using the AML1-ETO quantitative kit of the present invention, since the degree of recombination of the AML1-ETO fusion gene which causes acute myeloid leukemia can be more easily and accurately quantified, it can be widely used for accurate diagnosis of acute myeloid leukemia. will be.n n n n AML1-ETO fusion gene, AML1-ETO standard plasmid DNA, ABL standard plasmid DNA
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107083417-A
priorityDate 2004-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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