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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_70f457aebc6ad4e5d734d086d01fd862
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-10
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filingDate 1993-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94c559f06f0a1df28d95365c41bb075d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4fea643f429b0c698a7ba2fc7d473a6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da0463e36536a1c2d288625e2a43e164
publicationDate 1994-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06269283-A
titleOfInvention Animal cell culture medium
abstract (57) [Summary] [Objective] To provide a material exhibiting an animal cell growth activity equivalent to transferrin when added to a medium containing fetal calf serum (FCS) to enhance the animal cell growth activity and added to a serum-free medium. . [Constitution] An animal cell culture medium containing a heme iron composition obtained by removing a part of globin chains from hemoglobin. [Effect] When the heme iron composition of the present invention is added in a small amount to the FCS-containing medium, the proliferation of animal cells is significantly enhanced, so that the amount of expensive FCS used can be reduced, and it can be used instead of transferrin in a serum-free medium. be able to.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10968429-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003508046-A
priorityDate 1993-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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