http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2622977-T3
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a490020fd2580d5f04cbe4ea55b65c3f |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-763 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-582 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-542 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-542 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-28 |
filingDate | 2010-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2017-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30ec32585fcde5abde30852e017246ad http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce1d8b460c7b7ff051740026f14d168d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_971493e96dffec1ce74fb1cc602501a9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20325d638d645cebfd3f5f54453a4a07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f85bad4199b2bcae7ad7a35c30b5ffe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2201d5613112cddba2a3fe192a37ff69 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef6c294be5baf0081cde26da64a0aed1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4b4c15f48fd141f34d751e77c9c3aa1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5493e9b5ce8a62175266572f004c855 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5ccde403a5663fa34714a405b065fa0 |
publicationDate | 2017-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-2622977-T3 |
titleOfInvention | Homogeneous tests with dissolution phase |
abstract | A test method for an analyte in a sample, the test method comprising: forming a reaction mixture in an aqueous solution, in any order or simultaneously adding sample, a specific chemiluminescent labeled binding partner, a binding partner specific labeled with activator, wherein the activator brand activates the chemiluminescent label, and a selective signal inhibitor, where all components are soluble in aqueous solution, where the specific binding partner labeled with chemiluminescent and the partner Specific binding labeled with activator bind to analyte present in the sample to form a binding complex; adding to the reaction mixture an activating solution, wherein the activating solution releases a detectable chemiluminescent signal correlated with the amount of specific binding partner labeled with chemiluminescent bound to analyte and specific binding partner labeled with activator bound to analyte in the mixture reaction, wherein the selective signal inhibitor is selected from the group consisting of ** Formula ** wherein: the chemiluminescent-labeled specific binding partner comprises a chemiluminescent label compound directly or indirectly connected to a binding torque member specific, wherein the chemiluminescent brand is selected from compounds of acidane cetenedithioacetal, acridan esters, thioesters of acridane, acridane sulfonamides, and derivatives of acridane enol of formula VIII: ** Formula ** wherein R1 is selected from alkyl, alkenyl groups , alkynyl, aryl and aralkyl of 1-20 carbon atoms, any of which may be substituted with 1-3 groups selected from carbonyl groups, carboxyl groups, tri (C1-C8 alkyl) silyl groups, an SO3- group, an OSO3-2 group, glycosyl groups, a PO3- group, a OPO3-2 group, halogen atoms, a hydroxyl group, a thiol group, amino groups, quaternary ammonium groups or quaternary phosphonium groups, wherein X is selected from alkyl, aryl, C1-C8 aralkyl groups, the alkyl groups having or aryl carboxyl of 1-20 carbon atoms, tri (C1-C8 alkyl) silyl groups, a SO3- group, glycosyl groups and phosphoryl groups of the formula PO (OR ') (OR ") wherein R' and R" are independently selected from the alkyl, cyanoalkyl, aryl and aralkyl C1-C8 groups, trialkylsilyl groups, alkali metal cations, alkaline earth cations, ammonium and trialkylphosphonium cations, wherein Z is selected from O and S atoms, wherein R6 is selected from alkyl, phenyl, benzyl, alkoxyalkyl and substituted C1-C4 carboxyalkyl groups os or unsubstituted, where R7-14 is each hydrogen or 1 or 2 alkyl, alkoxy, hydroxy and halogen substituents are selected and the rest of R7-14 is hydrogen or where each of R7-14 is hydrogen and R1 it is a labeling substituent or wherein one of R7-14 is a labeling substituent and the others of R7-14 are hydrogen. wherein the specific binding partner labeled with activator comprises a compound with activator label directly or indirectly connected to a member of a specific binding pair wherein the activator brand is selected from transition metal salts, transition metal complexes and enzymes , wherein the activator brand has peroxidase activity, and wherein the activator solution comprises a peroxide compound. |
priorityDate | 2009-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 447.