http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1072272-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f23524351672b305a775d2f1458d2cdf
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-574
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K39-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-531
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-574
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-18
filingDate 1998-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffd8ff8df5ab5e0a42ce35bd8272772c
publicationDate 2001-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1072272-A1
titleOfInvention Method for producing a specific antiserum against the universal tumorous antigen and method for diagnosing malignant tumours using said antiserum
abstract The present invention pertains to the field of medicine and may be used for producing a specific antiserum as well as for carryingnout immunological diagnoses of malignant tumours. This method for producing an antiserum involves sampling an embryo at the foetalnstage from animals of a same genetic type so as to obtain a cell suspension. After immunisation, this method involves sampling spleenncells from the animal, separating lymphocytes and immunising the animal of the same genetic line using the lymphocyte suspension. Annantiserum is then obtained and cells originating from healthy organs of the same animals are added to said antiserum. The mixture is finallyndecanted and the liquid located above the sediments is filtered. In order to carry out a diagnosis, the filtrate is added to the subject's bloodnand the results are obtained by immuno-fluorescence, by blood tests or using other methods of immunological diagnosis. It it thus possiblento diagnose a tumour when the reliable values obtained differ from reference values.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101353629-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006128715-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006128715-A2
priorityDate 1998-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.