LU99_SCN5A-R282H_trans
LUMCi004-A-6
General
Cell Line |
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hPSCreg name | LUMCi004-A-6 |
Cite as: | LUMCi004-A-6 |
Alternative name(s) |
LU99_SCN5A-R282H_trans
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines | No similar lines found. |
Last update | 30th September 2024 |
User feedback | |
Provider |
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Generator | Leiden University Medical Center (LUMC) |
External Databases |
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BioSamples | SAMEA116100394 |
General Information |
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* Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
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Subclone of |
Donor Information
General Donor Information |
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Sex | female |
Ethnicity | caucasian |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Family history | No |
Is the medical history available upon request? | No |
Is clinical information available? | No |
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 | SAMEA5032583 |
Ethics
Also have a look at the ethics information for the parental line
LUMCi004-A
.
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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The source cell information can be found in the parental cell line
LUMCi004-A.
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Reprogramming method |
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Vector type | None |
Vector free reprogramming |
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Type of used vector free reprogramming factor(s) |
mRNA
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Other |
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Derived under xeno-free conditions |
Unknown |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Medium |
Other medium:
Base medium: StemFlex Medium
Main protein source: Fetal bovine serum Serum concentration: % |
Characterisation
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
Normal, 46, XX
Karyotyping method:
G-Banding
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Other Genotyping (Cell Line) |
Genetic Modification
Disease/phenotype related modifications |
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