ISTEMi015-A-1

4603c53_LC3

General

Cell Line

hPSCreg name ISTEMi015-A-1
Cite as:
ISTEMi015-A-1
Alternative name(s)
4603c53_LC3
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 2nd February 2026
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Provider

Generator Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
Owner Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
Distributors
Derivation country France

External Databases

BioSamples SAMEA120561741

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

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Family history Clinically unaffected; father of two affected daughters (GM04601, GM04602); affected spouse is GM04608; see GM04604 lymphocyte
Is clinical information available? Clinically unaffected; father of two affected daughters (GM04601, GM04602); affected spouse is GM04608; see GM04604 lymphocyte

External Databases (Donor)

BioSamples SAMEA120558811

Ethics

Also have a look at the ethics information for the parental line ISTEMi015-A .
Is there an MTA available for the cell line? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? For integration into the AAVS1 gene, a home-made plasmid was used; for the HiBiT part of the complete plasmid, Promega products were used
Are you aware of any constraints on the use or distribution of the cell line from the owner or any parties identified in the query above? No

hIPSC Derivation

General

The source cell information can be found in the parental cell line ISTEMi015-A.

Reprogramming method

Vector free reprogramming

Other

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

Culture Conditions

Surface coating Vitronectin
Feeder cells
No
Passage method Mechanically
CO2 Concentration 5 %
Medium Other medium:
Base medium: StemMACS™ iPS-Brew Basal Medium XF, human
Main protein source:
Serum concentration: %
Supplements
StemMACS™ iPS-Brew Supplement XF (50×), human 10 ml
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line?
No
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
SSEA-3
Yes
SSEA-4
Yes
POU5F1 (OCT-4)
Yes
TRA 1-60
Yes
TRA 1-81
Yes
NANOG
Yes
Morphology pictures
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
FOXA2
Yes
SOX17
Yes
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Marker Expressed
ACTA2
Yes
Brachyury
Yes
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation
Marker Expressed
Tuj1
Yes
PAX6
Yes

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XY
Passage number: 43
Karyotyping method: mFISH

Other Genotyping (Cell Line)

Is there genome-wide genotyping or functional data available?
Yes
SNP typing array
no mutation

Genetic Modification

Genetic modifications not related to a disease
MAP1LC3A (target)
Transgene expression
19q13.42
CRISPR–Cas9 was used to integrate, at the chromosome 19q13.42 safe harbor locus, a Promega-derived plasmid fragment containing the HiBiT tag and the MAP1LC3B gene for quantitative autophagy assessment
CRISPR-associated (CRISPR/Cas) System