Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_81ff2fb1401923e9777f848215eb575f http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_620939cea0c53e7263e5c04588ec80bb |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2201-0484 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2201-0446 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-821 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-973 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-808 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-807 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-809 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-805 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-966 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2021-6419 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-963 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2021-6421 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6428 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6452 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6458 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-25 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 |
filingDate |
1984-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c10215f068b63f924a9ede2dd605bf88 |
publicationDate |
1985-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
EP-0154743-A2 |
titleOfInvention |
Method and apparatus for automated double fluorochromization analysis in lymphocytotoxicity testing |
abstract |
An automated system for rapid sequential photometric analysis of a collection of double fluorochrome stained lymphocyte specimens, useful for antibody screening or lymphocytotoxicity analysis. The specimens are sequentially alternately irradiated with light of two distinguishable wavelengths, producing fluorescence at two distinguishable wavelengths. The fluorescent emission light intensity for each irradiation of each specimen is measured using a photometer and computer. The computer controls the synchronization of the irradiation through alternately selected condenser sets with the sequential movement of specimens Into the optical path of the irradiating and detected light, and calculates the ratio of the light intensities emitted from each specimen at the two selected fluorescent light wavelengths. These ratios are compared against a control ratio (for lymphocytotoxicity analysis) to classify the specimen. Also described is a method of preparing specimens for such analysis, which requires that a complement be added to the first staining solution after the latter is applied to the specimens, then this combination agitated, and then the second staining solution added and the specimen incubated. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0266881-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9310437-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-2215838-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-2196734-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-2215838-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0266881-A2 |
priorityDate |
1983-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |