EDi001-B-1
AST18-7A
Gene-edited iPSC line
The cell line is not available.
General#
Cell Line |
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| hPSCreg Name | EDi001-B-1 |
| Alternative name(s) |
AST18-7A
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| Cell line type | Human induced pluripotent stem cell (hiPSC) |
Provider |
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| Depositor | University of Edinburgh (ED) |
| Distributors |
EBiSC
European Collection of Authenticated Cell Cultures (ECACC)
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External Databases |
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| hPSCreg | EDi001-B-1 |
| BioSamples | SAMEA7111750 |
| CLO | CLO_0103009 |
| Cellosaurus | CVCL_A1XP |
| Wikidata | Q105506809 |
General Information |
|
| Publications | View all related publications on hPSCreg (2) |
| * Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
|
| Subclone of | (not in EBiSC, see EDi001-B in hPSCreg) |
Donor Information#
General Donor Information |
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| Sex | female |
Phenotype and Disease related information (Donor) |
|
| Diseases | A disease was diagnosed.
|
| Family history | Strong family history of Parkinson’s disease due to autosomal dominant inheritance of SNCA triplication |
| Is the medical history available upon request? | Y Mov Disord. 2011 Sep;26(11):2134-6. doi: 10.1002/mds.23776 |
Donor Relations |
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| Other cell lines of this donor | |
| All cell lines of this donor's relatives |
Has daughter:
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External Databases (Donor) |
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| BioSamples | SAMEA3319991 |
hIPSC Derivation#
General |
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More source cell information can be found in the parental cell line
EDi001-B in hPSCreg.
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Reprogramming method |
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| Vector type | Integrating |
| Vector | Virus (Retrovirus) |
| Genes | |
| Is the used vector excisable? |
Unknown |
| Absence of reprogramming vector(s)? |
Unknown |
| Reprogramming vectors silenced? |
Yes |
| Methods used |
RT-PCR
|
| Notes on reprogramming vector silencing | See Devine et al 2011 |
Vector free reprogramming |
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Other |
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| Derived under xeno-free conditions |
No |
| Derived under GMP? |
No |
| Available as clinical grade? |
No |
Culture Conditions#
The following are the depositor culture conditions, they do not refer to any specific batch.
| Surface coating | Laminin |
| Feeder cells |
No |
| Passage method |
Enzyme-free cell dissociation
EDTA
|
| O2 Concentration | 21 % |
| CO2 Concentration | 5 % |
| Medium |
Other medium:
Base medium: StemMACS™ iPS-Brew XF
Main protein source: Serum concentration: % |
Characterisation#
Analysis of Undifferentiated Cells
| Marker | Expressed | Immunostaining | RT-PCR | FACS | Enzymatic Assay | Expression Profiles |
| NANOG |
Yes |
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| POU5F1 (OCT-4) |
Yes |
|
Differentiation Potency
Genotyping#
Karyotyping (Cell Line) |
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| Has the cell line karyotype been analysed? |
Yes
No gross chromosomal abnormalities.
Karyotyping method:
Molecular karyotyping by SNP array
http:// |
Other Genotyping (Cell Line) |
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Genetic Modification#
| Disease/phenotype related modifications |
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