http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20120041091-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_feb03de036e93e10c4497dcbf96d3911 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-1866 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-18 |
filingDate | 2011-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ef01f2f64a06583275726f4b926e3b4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e81721b84a63f2270197362adbf856ff http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab6ab71ebe603f9741de1f218fd7644b |
publicationDate | 2012-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-20120041091-A |
titleOfInvention | Storage solution of seaweed used as biomarker for water toxicity evaluation and storage method of seaweed |
abstract | The present invention is a solution formed by dissolving an alkali metal salt of hydrazonic acid in a brine having a salt concentration of 25 ~ 45 ‰, the concentration of the alkali metal salt of hydrazonic acid in the solution is 0.01 ~ 1 It provides a blue storage solution, characterized in that the ppb. In addition, the present invention is a method for storing the seaweed used as a biomarker of water toxicity evaluation, comprising the steps of (a) preparing the seaweed; And (b) storing the prepared seaweed in a container containing the storage solution of the seaweed and storing it under refrigerated conditions at 0 ° C to 10 ° C. In the case of storing the seaweed using the storage solution of the seaweed according to the present invention, unlike the conventional storage method, it does not require the light irradiation dose, the air generator and the exchange of a certain range of intensity range, and thus continuously maintain the cultured seaweed as a test organism There is an advantage to solve the economic cost and labor shortage. In addition, the experiment can be performed at any time the water toxicity evaluator desired date, saving time. As a result, it is possible to increase the utilization of the method for evaluating water toxicity using already developed seaweed. |
priorityDate | 2010-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 73.