113-8, LUMC0113iATAX08	
    			    			
                LUMCi002-C            
            
        General
| Cell Line | |
| hPSCreg name | LUMCi002-C | 
| Cite as: | LUMCi002-C (RRID:CVCL_VE44) | 
| Alternative name(s) | 
	113-8, LUMC0113iATAX08	 | 
| Cell line type | Human induced pluripotent stem cell (hiPSC) | 
| Similar lines | LUMCi003-A (114-1, LUMC0114iCTRL01) LUMCi003-B (114-2, LUMC0114iCTRL02) HIHDNDi001-A (A30P-3, SNCA3, Tue_020_A) Donor's gene variants: SNCA, SNCA, SNCA Donor diseases: autosomal dominant Parkinson disease 1 HIHDNDi001-B (A30P-4, SNCA4, Tue_020_B) Donor's gene variants: SNCA, SNCA, SNCA Donor diseases: autosomal dominant Parkinson disease 1 HDZi003-A (hiPSC NP0038) Donor's gene variants: TMEM43 Donor diseases: arrhythmogenic right ventricular dysplasia 5 RNRMUi005-A (EB-iPSC-d4, RDEB-iPSC-d4) Donor diseases: Epidermolysis Bullosa Simplex recessive dystrophic epidermolysis bullosa | 
| Last update | 17th August 2022 | 
| User feedback | |
| Provider | |
| Generator | Leiden University Medical Center (LUMC) | 
| Derivation country | Netherlands | 
| External Databases | |
| Cellosaurus | CVCL_VE44 | 
| BioSamples | SAMEA6456117 | 
| Wikidata | Q54903272 | 
| General Information | |
| Publications | |
| * Is the cell line readily obtainable for third parties? | Yes Research use: allowed Clinical use: not allowed Commercial use: allowed | 
Donor Information
| General Donor Information | |
| Sex | male | 
| Ethnicity | Caucasian | 
| Phenotype and Disease related information (Donor) | |
| Diseases | A disease was diagnosed. | 
| Karyotyping (Donor) | |
| Has the donor karyotype been analysed? | Yes 
												46 XY
											 
											Karyotyping method:
											Molecular karyotyping by SNP array											
											 http:// | 
| Donor Relations | |
| Other cell lines of this donor | |
| All cell lines of this donor's relatives | 
												Has sister:
										 | 
| External Databases (Donor) | |
| BioSamples | SAMEA6456114 | 
Ethics
| Has informed consent been obtained from the donor of the embryo/tissue from which the pluripotent stem cells have been derived? | Yes | 
| Was the consent voluntarily given? | Yes | 
| Has the donor been informed that participation will not directly influence their personal treatment? | Yes | 
| Can you provide us with a copy of the Donor Information Sheet provided to the donor? | Yes | 
| Do you (Depositor/Provider) hold the original Donor Consent Form? | Yes | 
| Please indicate whether the data associated with the donated material has been pseudonymised or anonymised. | pseudonymised | 
| Does consent explicitly allow the derivation of pluripotent stem cells? | Yes | 
| Does consent prevent CELLS DERIVED FROM THE DONATED BIOSAMPLE from being made available to researchers anywhere in the world? | No | 
| How may genetic information associated with the cell line be accessed? | Controlled Access | 
| Will the donor expect to receive financial benefit, beyond reasonable expenses, in return for donating the biosample? | No | 
| Has a favourable opinion been obtained from a research ethics committee, or other ethics review panel, in relation to the Research Protocol including the consent provisions? | Yes | 
| Name of accrediting authority involved? | LUMC medical ethics committee | 
| Approval number | NL45478.058.13/P13.080 | 
| Has a favourable opinion been obtained from a research ethics committee, or other ethics review panel, in relation to the PROPOSED PROJECT, involving use of donated embryo/tissue or derived cells? | Yes | 
| Name of accrediting authority involved? | LUMC medical ethics committee | 
| Approval number | NL45478.058.13/P13.080 | 
| For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? | 
hIPSC Derivation
| General | |
| Source cell type | |
| Reprogramming method | |
| Vector type | Non-integrating | 
| Vector | Sendai virus | 
| Is reprogramming vector detectable? | No | 
| Methods used | 
	Immunostaining, RT-PCR	 | 
| Vector free reprogramming | |
| Other | |
| Derived under xeno-free conditions | Unknown | 
| Derived under GMP? | Unknown | 
| Available as clinical grade? | Unknown | 
Culture Conditions
| Surface coating | Matrigel/Geltrex | 
| Feeder cells | No | 
| Passage method | Enzyme-free cell dissociation | 
| CO2 Concentration | 5 % | 
| Medium | mTeSR™ 1 | 
Characterisation
Analysis of Undifferentiated Cells
| Marker | Expressed | Immunostaining | RT-PCR | Flow Cytometry | Enzymatic Assay | Expression Profiles | 
| SSEA-4 | Yes |  | ||||
| SOX2 | Yes |  | ||||
| NANOG | Yes |  |  | |||
| POU5F1 (OCT-4) | Yes |  |  | 
Genotyping
| Karyotyping (Cell Line) | |
| Has the cell line karyotype been analysed? | Yes | 
| Other Genotyping (Cell Line) | |

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