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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_08dde60e3e0ca1e6ffaa5143e5c8477a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-02
filingDate 2010-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e107a9cfd73877c359e9fe20f39835d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1f07bf9e6495a0b0e5270527590b02d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbac1922d89e8baca050e6f178b07da9
publicationDate 2014-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102337321-B
titleOfInvention Kit for detecting phagocytic activity of monocyte
abstract The invention relates to a kit for detecting phagocytic activity of a monocyte, comprising tumor cells stained with a dye. The rapid detection of high flux of the monocyte is realized by using the kit. The detection with using the kit can be carried out in a 96 orifice plate and comprises the following steps: a sample and a reagent in the kit are added in the 96 orifice plate for reacting for a certain time, then a microplate reader or a fluorospectro photometer is used to detect OD values of each orifice, and the phagocytic activity of the monocyte in each orifice is calculated according to the OD values. The microplate reader and other instruments are used for reading, compared with artificial reading with microscopes, time is saved, personal errors are prevented, and accuracy of the detection and the detection efficiency are improved. Only 30 individuals can be detected through the traditional method, however, 2-300 samples and 150-300 individuals can be detected through the invention every day, so that the detection efficiency is greatly improved.
priorityDate 2010-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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