http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61195685-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12M41-36
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-24
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
filingDate 1985-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49e21c2de6539344c7f57682f24a5b46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2865c5cf984590fcfdba820cf5753ae
publicationDate 1986-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61195685-A
titleOfInvention Vessel for examination of specimen
abstract PURPOSE: To enable the accurate examination of a specimen, by using a plastic vessel for the determination of bacteria contained therein, wherein at least the inner wall of the space in the vessel is coated with an antistatic agent. n CONSTITUTION: The examination vessel 1 is a molded vessel of a transparent polystyrene, and the whole circumference of the inner wall of the vessel 1 is coated with Corcoat (a permanent antistatic coating). The antistatic layer 8 is formed by spraying the antistatic coating). The antistatic layer 8 is formed by spraying the antistatic agent to the whole surface of the inner wall of the vessel 1, and drying the agent. The antistatic agent may be an amorphous silica, and the thin film of the silica has excellent heat-resistance, water- resistance and light-transmittance. A specimen composed of bacterial cells and a suppressing factor is placed in the hollow part 2, and is irradiated with light from the light source 3. The scattered light is detected by the sensor 7 to determine the proliferation rate of the bacteria in the specimen 2. n COPYRIGHT: (C)1986,JPO&Japio
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10677727-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021152335-A1
priorityDate 1985-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 23.