AICS-0097-157
UCSFi001-A-91
General
Cell Line |
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hPSCreg name | UCSFi001-A-91 |
Cite as: | UCSFi001-A-91 |
Alternative name(s) |
AICS-0097-157
|
Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines | No similar lines found. |
Last update | 5th November 2024 |
Notes | Subclone of UCSFi001-A-4 Part of disease collection Cardiomyopathy AICS-0097 |
User feedback | |
Provider |
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Generator | Allen Institute for Cell Science (AICS) |
Distributors | |
Derivation country | United States |
External Databases |
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BioSamples | SAMEA116327873 |
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
|
Subclone of |
Donor Information
General Donor Information |
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Sex | male |
Ethnicity | Asian |
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? | Limited clinical information - EKG |
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 | SAMEA5843920 |
Ethics
Also have a look at the ethics information for the parental line
UCSFi001-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
UCSFi001-A.
|
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Reprogramming method |
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Vector type | Non-integrating |
Vector | Episomal |
Vector free reprogramming |
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Other |
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Derived under xeno-free conditions |
Unknown |
Derived under GMP? |
Unknown |
Available as clinical grade? |
Unknown |
Culture Conditions
Medium |
mTeSR™ 1
|
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
46,XY
|
Other Genotyping (Cell Line) |
Genetic Modification
Disease/phenotype related modifications |
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