LUMC0004iCTRL10
LUMCi029-B
General
Donor Information
General Donor Information |
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Sex | male |
Ethnicity | unknown |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Family history | N/A |
Is the medical history available upon request? | No |
Is clinical information available? | No |
Karyotyping (Donor) |
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Has the donor karyotype been analysed? |
No
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Other Genotyping (Donor) |
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Is there genome-wide genotyping or functional data available? |
No
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Donor Relations |
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Other cell lines of this donor | |
External Databases (Donor) |
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BioSamples | SAMEA6673739 |
Ethics
Has informed consent been obtained from the donor of the embryo/tissue from which the pluripotent stem cells have been derived? | No |
Was the consent voluntarily given? | No |
Has the donor been informed that participation will not directly influence their personal treatment? | No |
Can you provide us with a copy of the Donor Information Sheet provided to the donor? | No |
Please provide contact information of the holder of the original Donor Information Sheet. | NA |
Do you (Depositor/Provider) hold the original Donor Consent Form? | No |
If you do not hold the Donor Consent Form, do you know who does? | No |
Alternatives to consent are available? | Yes |
Alternatives to consent | Regulations LUMC regarding the use of surgical waste material for research (in Dutch) |
Alternative consent approval number | |
Is there other documentation provided to the donor for consenting purposes? | No |
Confirm that consent was obtained by a qualified professional | No |
Has the donor agreed to be re-contacted? | Unknown |
Has the donor been informed about how her/his data will be protected? | No |
Please indicate whether the data associated with the donated material has been pseudonymised or anonymised. | anonymised |
Does consent explicitly allow the derivation of pluripotent stem cells? | No |
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? | No information |
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? | No |
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? | Leiden University Medical Center Ethical Commitee |
Approval number | Paraplu 13080 |
Do you have obligations to third parties in regard to the use of the cell line? | No |
Are you aware of any further constraints on the use of the donated embryo/tissue or derived cells? | Yes |
Further constraints on use | For commercial use a license for the reprogramming vectors is required. |
Is there an MTA available for the cell line? | Yes |
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? | Christopher Baum Hannover Medical School, Germany |
Are you aware of any constraints on the use or distribution of the cell line from the owner or any parties identified in the query above? | Yes |
Constraints for use or distribution | For commercial use a license for the reprogramming vectors is required. |
hIPSC Derivation
General |
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Source cell type | |
Source cell origin |
An organ that constitutes the external surface of the body. It consists of the epidermis, dermis, and skin appendages.
Synonyms
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Reprogramming method |
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Vector type | Integrating |
Vector | Virus (Lentivirus) |
Genes | |
Is the used vector excisable? |
Yes |
Absence of reprogramming vector(s)? |
No |
Reprogramming vectors silenced? |
Unknown |
Notes on reprogramming vector silencing | In addition to OSKM lentivirus carries a tomato signal which can be used to check transgene silencing if necessary. |
Vector map | |
Vector free reprogramming |
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Type of used vector free reprogramming factor(s) |
None
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Other |
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Selection criteria for clones | Morphology |
Derived under xeno-free conditions |
No |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Vitronectin |
Feeder cells |
No |
Passage method |
Enzyme-free cell dissociation
Gentle Cell Dissociation Reagent
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CO2 Concentration | 5 % |
Medium |
mTeSR™ 1
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Characterisation
Analysis of Undifferentiated Cells
Marker | Expressed | Immunostaining | RT-PCR | Flow Cytometry | Enzymatic Assay | Expression Profiles |
TRA 1-81 |
Yes |
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POU5F1 (OCT-4) |
Yes |
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NANOG |
Yes |
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SOX2 |
Yes |
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SSEA-3 |
Yes |
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SSEA-4 |
Yes |
Pluripotency Score | Novelty Score | |
22.49 | 1.19 |
Differentiation Potency
In vitro spontaneous differentiation
Marker | Expressed |
alpha fetoprotein (AFP) |
Yes |
Protocol or reference
LUMC0004iCTRL10 spondiff.pdf
Spontaneous Diff of LUMC0004iCTRL10 p11
In vitro spontaneous differentiation
Marker | Expressed |
PECAM1(CD31) |
Yes |
Protocol or reference
LUMC0004iCTRL10 spondiff.pdf
Spontaneous Diff of LUMC0004iCTRL10 p11
In vitro spontaneous differentiation
Marker | Expressed |
beta-III tubulin |
Unknown |
Protocol or reference
LUMC0004iCTRL10 spondiff.pdf
Spontaneous Diff of LUMC0004iCTRL10 p11
Microbiology / Virus Screening |
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Mycoplasma | Negative |
Genotyping
Karyotyping (Cell Line) |
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Has the cell line karyotype been analysed? |
Yes
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Other Genotyping (Cell Line) |
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