CEBe033-A-12

SA001 DP427 KO1

General

iPSC Line

hPSCreg name CEBe033-A-12
Cite as:
CEBe033-A-12
Alternative name(s)
SA001 DP427 KO1
iPSC line type Human embryonic stem cell (hESC)
Similar iPSC lines
CEBe033-A-13
(SA001 DP427 KO2)
CEBe033-A-14
(SA001 DP140 KO1)
CEBe033-A-15
(SA001 DP140 KO2)
CEBe033-A-16
(SA001 DP140 KO3)
CEBe033-A-17
(SA001 DP71 KO1)
CEBe033-A-18
(SA001 DP71 KO2)
CEBe033-A-19
(SA001 DP71 KO3)
CEBe033-A
(SA001)
CEBe033-A-8
(SA001_KO_HGPRT_1)
CEBe033-A-9
(SA001_KO_HGPRT_2)
CEBe033-A-10
(SA001_WT_HGPRT_1)
CEBe033-A-11
(SA001_WT_HGPRT_2)
CEBe033-A-2
(SA001 Shank3 hetero1)
CEBe033-A-3
(SA001 Shank3 Hetero2)
CEBe033-A-4
(SA001 Shank3 Hetero3)
CEBe033-A-5
(SA001 Shank3 Homo1)
CEBe033-A-6
(SA001 Shank3 Homo2)
CEBe033-A-7
(SA001 Shank3 Homo3)
CEBe033-A-1
(GBA1_hESC_GBA#1-/-_10.18.11)
ITXi006-A-1
(IM-R406W)
Last update 23rd September 2025
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Provider

Generator Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)

External iPSC Databases

BioSamples SAMEA120250250

General iPSC Information

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

iPSC Genetic Modification

Disease/phenotype related modifications
Synonyms
  • DMD
  • Severe dystrophinopathy, Duchenne type
Genetic modifications
DMD (target)
Gene knock-out
Xp21.2-p21.1
target deletion into exon 3
CRISPR-associated (CRISPR/Cas) System

Donor Information

General Donor Information

Sex male

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Other Genotyping (Donor)

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

External Databases (Donor)

BioSamples SAMEA104132810

Ethics

Also have a look at the ethics information for the parental line CEBe033-A .
Is there an MTA available for the cell line? Yes
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? Yes
Constraints for use or distribution Work with human embryonic stem cells requires prior approval by local ethics committees.

hESC Derivation

The source cell information can be found in the parental cell line CEBe033-A.

iPSC Culture Conditions

Surface coating Vitronectin
Feeder cells
No
Passage method Mechanically
CO2 Concentration 5 %
Medium Other medium:
Base medium: StemMacs IPS-Brew XF
Main protein source:
Serum concentration: %
Supplements
StemMacs IPS-Brew XF Supplement 10 ml
Has Rock inhibitor (Y27632) been used at passage previously with this iPSC line?
No
Has Rock inhibitor (Y27632) been used at cryo previously with this iPSC line?
No
Has Rock inhibitor (Y27632) been used at thaw previously with this iPSC line?
Yes

iPSC Characterisation

Analysis of undifferentiated iPSCs
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
NANOG
Yes
SSEA-4
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
SOX17
Yes
FOXA2
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
TUBB3
Yes
PAX6
Yes

Genotyping

Karyotyping (iPSC Line)

Has the iPSC line karyotype been analysed?
Yes
46,XY
Passage number: 88
Karyotyping method: Spectral karyotyping

Other Genotyping (iPSC Line)

Is there genome-wide genotyping or functional data available?
Yes
SNP typing array
No mutations