AICS-0097-157

General

Cell Line

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
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Provider

Generator Allen Institute for Cell Science (AICS)
Distributors
Derivation country United States

External Databases

BioSamples SAMEA116327873

General Information

* 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

Sex male
Ethnicity Asian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Family history N/A
Is the medical history available upon request? No
Is clinical information available? Limited clinical information - EKG

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

Donor Relations

Other cell lines of this donor

External Databases (Donor)

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

The source cell information can be found in the parental cell line UCSFi001-A.

Reprogramming method

Vector type Non-integrating
Vector Episomal

Vector free reprogramming

Other

Derived under xeno-free conditions
Unknown
Derived under GMP?
Unknown
Available as clinical grade?
Unknown

Culture Conditions

Medium mTeSR™ 1

Characterisation

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XY

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Cardiomyopathy
Synonyms
  • Cardiomyopathies
Genetic modifications
MYH7 (target)
Variant
14q11.2
G256E/WT
NM_000257.4(MYH7):c.767G>A(p.Gly256Glu)