http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103865956-B

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Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-867
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-0793
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-10
filingDate 2013-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103865956-B
titleOfInvention Utilize the method that recombinant slow virus induced nerve stem cells breaks up to dopaminergic neuron
abstract The present invention relates to a kind of biotechnology, a kind of method utilizing gene recombined virus induced nerve stem cells to break up to dopaminergic neuron: recombined lentivirus vector builds;The separation of neural stem cell, cultivate and identify;Recombinant virus transfection NSCs;The qualification of recombinant slow virus transfection NSCs;Recombinant virus transfection NSCs: take the digestion of the NSCs after passing on 3 times and be prepared as single cell suspension, be seeded in culture plate;Transfection TH+Brn4 gene recombinaton slow virus;Add slow virus and ploybrene, after rocking mixing, culture plate is put in incubator and cultivate, after 12 hours, change fresh division culture medium;Screen with puromycin, to obtain the cell of stable transfection simultaneously;It is an advantage of the current invention that: by building the slow virus carrier of genes of interest TH and Brn4, after transfection NSCs, allogenic gene can be expressed at cell inner stablity;A high proportion of TH positive dopaminergic neuron is produced after differentiation;Brn4 can promote the high expressed of neurotrophic factor, and has the function of inhibited apoptosis.
priorityDate 2013-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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