C27, iPS-27
MSKi002-A
General
Cell Line |
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hPSCreg name | MSKi002-A |
Cite as: | MSKi002-A (RRID:CVCL_D0JC) |
Alternative name(s) |
C27, iPS-27
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines | No similar lines found. |
Last update | 9th August 2023 |
User feedback | |
Provider |
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Generator | Memorial Sloan Kettering Cancer Center (MSK) |
External Databases |
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BioSamples | SAMEA114243953 |
Cellosaurus | CVCL_D0JC |
Wikidata | Q123032724 |
General Information |
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Publications | |
* Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Additional restrictions:
Donor cells were from ATCC (MRC-5; CCL-171). |
Donor Information
General Donor Information |
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Sex | male |
Ethnicity | White, 14 weeks gestation |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Karyotyping (Donor) |
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Has the donor karyotype been analysed? |
Unknown
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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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External Databases (Donor) |
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BioSamples | SAMEA114243995 |
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? | No |
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. | Donor cell was purchased from ATCC (MRC-5 CCL-17). Please contact ATCC at www.atcc.org. |
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 | Please contact ATCC at www.atcc.org. |
Alternatives to consent are available? | Yes |
Alternatives to consent | |
Alternative consent approval number | |
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 expressly prevent the derivation of pluripotent stem cells? | No |
Does consent pertain to a specific research project? | 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 prevent CELLS DERIVED FROM THE DONATED BIOSAMPLE from being made available to researchers anywhere in the world? | No |
Does consent permit research by | |
an academic institution? | Yes |
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 |
Does the consent anticipate that the donor will be notified of results or outcomes of any research involving the donated samples or derived cells? | 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 |
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 line name | MRC5 |
Source cell type |
Homo sapiens (human) lung; fibroblast; normal cell line. The MRC-5 cell line was derived from normal lung tissue of a 14-week-old male fetus by J.P. Jacobs in September of 1966.
Synonyms
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Source cell line vendor | ATCC |
Reprogramming method |
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Vector type | Integrating |
Vector | Virus (Lentivirus) |
Genes | |
Is the used vector excisable? |
No |
Absence of reprogramming vector(s)? |
No |
Reprogramming vectors silenced? |
Unknown |
Notes on reprogramming vector silencing | Pronounced lentiviral vector silencing was a characteristic of successfully reprogrammed hiPSC clones, but lack of complete silencing. |
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 | Gene Expression Profiling; Teratoma Formation; In Vitro Differentiation; Vector silencing. |
Derived under xeno-free conditions |
No |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Non coated | |||||||||||||||
Feeder cells |
on a feeder layer of mitomycin C-treated mouse embryonic fibroblasts (MEFs) |
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Passage method |
Enzymatically
Dispase
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O2 Concentration | 21 % | |||||||||||||||
CO2 Concentration | 5 % | |||||||||||||||
Medium |
Other medium:
Base medium: DMEM/F12
Main protein source: Knock-out serum replacement Serum concentration: 20 % Supplements
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Has Rock inhibitor (Y27632) been used at passage previously with this cell line? | Yes |
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Has Rock inhibitor (Y27632) been used at cryo previously with this cell line? | No |
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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 |
TRA 1-60 |
Yes |
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TRA 1-81 |
Yes |
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SSEA-3 |
Yes |
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NANOG |
Yes |
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Score:
Marker | Present | Absent |
mCpG | ||
OCT4 |
Differentiation Potency
In vivo teratoma
Morphology
From Left to Right: neuroectoderm(black arrow),smooth muscle(blank arrow),and primitive myxoid tissue (arrowhead), 4x. Pigmented epithelial tissue compatible with retinal neuroectoderm, 40x. Intestinal like epithelium including goblet cells (endoderm), 40x. Smooth muscle tissue, 20x. Inset demonstrates a high power image of immature mesenchymal tissue, potentially cartilage (40x).
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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