AUMCi015-A-1

LMNA-D44-PE1-A43B

The cell line is not validated yet.

General

Cell Line

hPSCreg name AUMCi015-A-1
Cite as:
AUMCi015-A-1
Alternative name(s)
LMNA-D44-PE1-A43B
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 19th March 2026
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Provider

Generator Amsterdam University Medical Centers (AUMC)
Owner Amsterdam University Medical Centers (AUMC)
Distributors
Derivation country Netherlands

External Databases

BioSamples SAMEA121979603

General Information

* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: not allowed
Commercial use: allowed
Additional restrictions:

The institute requires an MTA for academic parties and a license for all commercial parties.

Subclone of

Donor Information

General Donor Information

Sex female
Ethnicity Caucasian

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • Congestive cardiomyopathy
  • Cardiomyopathy, dilated
  • Stretched and thinned heart muscle
  • DCM
show more synonyms
Genetic variants
1q21
NM_170707.4:c.1477C>T
NP_733821.1:p.Gln493Ter
Heterozygous
VCV000014514.5
Family history Brother died of DCM due to the same mutation

Other Genotyping (Donor)

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

External Databases (Donor)

BioSamples SAMEA120404906

Ethics

Also have a look at the ethics information for the parental line AUMCi015-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? invitrogen
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 AUMCi015-A.
Passage number reprogrammed 1

Reprogramming method

Vector type Non-integrating
Vector Sendai virus
Genes
Is reprogramming vector detectable?
No
Methods used
Immunostaining, RT-PCR
Notes on reprogramming vector detection Parental line has been tested, genetic modified line has not been retested
Files and images showing reprogramming vector expressed or silenced

Vector free reprogramming

Other

Selection criteria for clones Based on morphology
Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzyme-free cell dissociation
EDTA
O2 Concentration 20 %
CO2 Concentration 5 %
Medium mTeSR™ 1
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
Yes
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
NANOG
Yes
POU5F1 (OCT-4)
Yes
SSEA-4
Yes
TRA 1-60
Yes
SOX2
Yes
Morphology pictures
Morphology prime-edited line
Differentiation Potency
Endoderm
Ont Id: NCIT_C12706
In vitro directed differentiation
Marker Expressed
LEFTY1
Yes
SOX17
Yes
Protocol or reference
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Marker Expressed
TBX6
Yes
HAND1
Yes
Protocol or reference
Cardiac Muscle Cell
Ont Id: CL_0000746
In vitro directed differentiation
Marker Expressed
ACTN1
Yes
Protocol or reference
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Marker Expressed
SOX1
Yes
OTX2
Yes
Protocol or reference

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XX
Passage number: p28
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • Congestive Cardiomyopathy
  • Dilated Cardiomyopathy
Genetic modifications
LMNA (target)
Isogenic modification
1q22
NM_170707.4:c.1477C>T
NP_733821.1:p.Gln493Ter
Homozygous
The heterozygous Q493X mutation has been corrected using the prime-editing method. The corresponding line is therefore homozygous wildtype for the C allele of the c.1477C>T. However a heterozygous synonymous mutation, c.1479G>A, has been introduced to mutate the PAM-sequence needed for editing.
Repaired