http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57125352-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_afd115dec46c157d3739020ebd4d866b |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-81 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-531 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-60 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-531 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-579 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-88 |
filingDate | 1981-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_887983d2375d9daab24a3556885bf669 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1eb3840eeeac8ffd6bae42138155a309 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51a8365cb879ec5eb45338d0e9474965 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a21ed34df660a93e570fe3e5b8e71e90 |
publicationDate | 1982-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-S57125352-A |
titleOfInvention | Method and kit for preparing sample used for testing endotoxin with water-insoluble antihomo alpha2-macroglobulin antibody |
abstract | PURPOSE:To prepare samples used for testing endotoxin without including any analysis disturbing component by a method wherein samples of blood plasma or blood producing agents are developed through a column filled with an antihomo alpha2-macroglobulin antibody which has become water-insoluble with crosslinked aryldextran. CONSTITUTION:A water-insoluble antibody 2 of 100-300 mesh, which is obtained by chemically combine an antihomo alpha2-macroglobulin antibody with aryldextran crosslinked with N,N'-methylenebis-acrylamido after having been treated with BrCN or so, is filled in a column 1 with an inner diameter of 7-12mm. by an amount of 2-4ml and then a tight stopper 4 is fitted. The above solidified antibody 2 is placed between a support plate 6 and a holding plate 5 in the column 1, while a lower buffer solution layer 8 is enclosed by a bottom cover 7 and supernatant fluid 3 also comprises buffer solution. Meanwhile, an ampul of water solution containing high molecular coloring materials to be added to sample and an ampul of buffer solution for developing are readied, so that a preparing kit is obtained as a set. Samples such as blood plasma are mixed with the above water solution containing the coloring materials and caused to flow down through the column, thereby to develop the sample with the developing solution. The eluted colored fractions are collected and then used as samples for testing. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H023168-Y2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S59154661-U |
priorityDate | 1981-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.