http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H06153944-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e4feda2a82a4adcd92a7619df2248333 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-465 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-24 |
| filingDate | 1992-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a2d553c602cfea58399a55987a986c9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9546206758af75711fcb56e50508c867 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a8d9bf5de13fe70aadf740efd03347a |
| publicationDate | 1994-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H06153944-A |
| titleOfInvention | Carbohydrate hydrolase |
| abstract | (57) [Summary] [Object] To provide a novel lacto-N-biosidase that is highly purified and suitable for industrial production. [Structure] The formula Galβ1-3GlcNAcβ1-R (R represents a sugar residue) acts on the sugar chain to hydrolyze only the lacto-N-bioside bond, and acts on the lacto-N-bioside bond. -Does not act on acetyllactosaminide binding, Also, the substrate specificity of acting on p-nitrophenyl-β-lacto-N-bioside to release Galβ1-3GlcNAc, optimum pH around pH 5.5, optimum temperature around 60 ° C, about 6 × 10. An exo-type sugar hydrolase having a molecular weight of 4 . [Effect] It is a reagent useful for elucidating the structure and function of complex sugar chains. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5908772-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0739983-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-1100878-C |
| priorityDate | 1992-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 193.