iEBS
MLi002-A
General
Cell Line |
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hPSCreg name | MLi002-A |
Cite as: | MLi002-A (RRID:CVCL_UJ78) |
Alternative name(s) |
iEBS
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines |
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Last update | 22nd May 2019 |
User feedback | |
Provider |
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Generator | Faculty of Medicine University of Ljubljana (ML) |
Owner | Faculty of Medicine University of Ljubljana (ML) |
Derivation country | Slovenia |
External Databases |
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BioSamples | SAMEA5340004 |
Cellosaurus | CVCL_UJ78 |
Wikidata | Q95990117 |
General Information |
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Publications | |
* Is the cell line readily obtainable for third parties? |
No |
Donor Information
General Donor Information |
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Sex | female |
Ethnicity | Caucasian |
Phenotype and Disease related information (Donor) |
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Diseases | A disease was diagnosed.
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Disease associated phenotypes |
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Karyotyping (Donor) |
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Has the donor karyotype been analysed? |
Unknown
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External Databases (Donor) |
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BioSamples | SAMEA5340319 |
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? | No |
Please provide contact information of the holder of the original Donor Information Sheet. | Hans Torma, Dermatology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden |
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? | Yes |
Please provide the contact information | Hans Torma, Dermatology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden |
Alternatives to consent | |
Confirm that consent was obtained by a qualified professional | Yes |
Has the donor agreed to be re-contacted? | Unknown |
Has the donor been informed about how her/his data will be protected? | Yes |
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? | Yes |
Does consent expressly prevent the derivation of pluripotent stem cells? | No |
Does consent pertain to a specific research project? | No |
Does consent permit unforeseen future research, without further consent? | No |
Does the consent permit uses of donated embryo/tissue or derived cell line intended for clinical treatment or human applications? | No |
Does consent expressly prevent development of commercial products? | Yes |
Does consent expressly prevent financial gain from any use of the donated embryo/tissue, including any product made from it? | Yes |
Does consent expressly permit storage of donated embryo/tissue for an unlimited time? | Yes |
Does consent expressly permit storage of cells derived from the donated embryo/tissue for an unlimited time? | Yes |
Does consent prevent the DONATED BIOSAMPLE from being made available to researchers anywhere in the world? | No |
Does consent prevent CELLS DERIVED FROM THE DONATED BIOSAMPLE from being made available to researchers anywhere in the world? | Yes |
Does consent permit research by | |
an academic institution? | Yes |
a public organisation? | Yes |
a non-profit company? | Yes |
a for-profit corporation? | 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? | 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? | No |
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? |
hIPSC Derivation
General |
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Source cell type |
The keratin-producing cells of the epidermis. They are the predominant cells of the epidermis that form in the deep basal layer of the stratified epithelium of the epidermis. They gradually migrate upward to the cornified layer of the epidermis undergoing characteristic changes.
Synonyms
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Source cell origin |
Removal of a portion of skin tissue, for microscopic examination.
Synonyms
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Passage number reprogrammed | 3 |
Reprogramming method |
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Vector type | Non-integrating |
Vector | Sendai virus |
Genes | |
Is reprogramming vector detectable? |
Yes |
Methods used |
PCR, RT-PCR, Sequencing
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Notes on reprogramming vector detection | CytoTune- iPS 2.0 Sendai Reprogramming kit from Invitrogen / After ten passages, the elimination of the SeV vectors was confirmed in the MLi002-A cell line by RT-PCR using specific primers |
Files and images showing reprogramming vector expressed or silenced | |
Vector free reprogramming |
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Other |
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Derived under xeno-free conditions |
Yes |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Matrigel/Geltrex |
Feeder cells |
Human fibroblast feeders |
Passage method |
Enzyme-free cell dissociation
Gentle Cell Dissociation Reagent
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O2 Concentration | 5 % |
CO2 Concentration | 5 % |
Medium |
mTeSR™ 2
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Has Rock inhibitor (Y27632) been used at passage previously with this cell line? | No |
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line? | No |
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line? | Yes |
Characterisation
Analysis of Undifferentiated Cells
Marker | Expressed | Immunostaining | RT-PCR | Flow Cytometry | Enzymatic Assay | Expression Profiles |
NANOG |
Yes |
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POU5F1 (OCT-4) |
Yes |
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TRA 1-60 |
Yes |
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TRA 1-81 |
Yes |
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Alkaline Phosphatase |
Yes |
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Differentiation Potency
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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