http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102494986-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac31afbea1cbbb03498644721ffb4a62 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N15-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N15-04 |
| filingDate | 2011-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_244ae35249f28af59b7c593a9a204ba1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da69b4fe3de56d7c5e04734c2f177eda http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae3e441fbb15367b59eb6b8ea5388a99 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58231ded6c092c1e02496106cc3935a1 |
| publicationDate | 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102494986-B |
| titleOfInvention | Method for determining floating percentage of microcystis |
| abstract | The invention relates to a method for determining floating percentage of microcystis. According to the method, a BG11 culture medium is prepared, and is sterilized; the sterilized BG11 culture medium is placed in a superclean bench and cooled; a sterile operation method is adopted to inoculate microcystis, wherein the inoculation amount is 10<4>-10<5> cells/mL; then the inoculated medium is placed in an illumination incubator with a set temperature of 25 DEG C and light intensity of 100 mumol/m<2>.s to carry out culture; after the microcystis grows to the logarithmic phase, the microcystis is conveyed to an illumination incubator with a certain temperature and a certain light intensity to carry out culture, and is taken once in a while, wherein the experimental temperature range is 0-30 DEG C, the light intensity range is 0-500 mumol/m<2>.s, and a certain temperature and a certain light intensity are required by the experiment; the microcystis liquid is sucked by a pipette gun, and a drip of the microcystis liquid is added in a cell counting plate, wherein the counting plate is the cell counting plate (CELL-VU), and the depth of the counting chamber of the cell counting plate is 0.02 mm; the cell counting plate is placed under the microscope, and the counting treatments are respectively performed on the floating microcystis and the total algae. |
| priorityDate | 2011-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415057377 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24504 |
Total number of triples: 18.