LUMCi004-A-4

LUMCi099_XPC_D10

General

Cell Line

hPSCreg name LUMCi004-A-4
Cite as:
LUMCi004-A-4 (RRID:CVCL_E4H5)
Alternative name(s)
LUMCi099_XPC_D10
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 11th May 2024
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Provider

Generator Leiden University Medical Center (LUMC)
Owner Leiden University Medical Center (LUMC)
Distributors
Derivation country Netherlands

External Databases

BioSamples SAMEA115580245
Cellosaurus CVCL_E4H5

General Information

* Is the cell line readily obtainable for third parties?
Yes
Cell line can only be used in: To be discussed with Karine Raymond
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Additional restrictions:

Under MTA request addressed to Karine Raymond

Subclone of

Donor Information

General Donor Information

Sex female
Ethnicity caucasian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Family history No
Is the medical history available upon request? No
Is clinical information available? No

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 SAMEA5032583

Ethics

Also have a look at the ethics information for the parental line LUMCi004-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?
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 LUMCi004-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 Enzyme-free cell dissociation
Gentle Cell Dissociation Reagent
O2 Concentration 20 %
CO2 Concentration 5 %
Medium mTeSR™ Plus
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
SSEA-4
Yes
NANOG
Yes
POU5F1 (OCT-4)
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Marker Expressed
GATA4
Yes
FOXA2
Yes
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Marker Expressed
Vimentin
Yes
CDX2
Yes
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Marker Expressed
Nestin
Yes
PAX6
Yes

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46, XX
Passage number: 24
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • XP group C
  • XP-C
  • XP3
  • XPC
  • XPCC
  • xeroderma pigmentosum III
  • xeroderma pigmentosum group C
  • xeroderma pigmentosum group type C
  • xeroderma pigmentosum, complementation group type C
  • xeroderma pigmentosum, group C
  • XP, Group C
  • xeroderma pigmentosum 3
  • xeroderma pigmentosum, complementation group C
  • xeroderma pigmentosum, type 3
show more synonyms
Genetic modifications
XPC (target)
Isogenic modification
3p25.1
c.1399C>T
p.Gln467X
Homozygous
Mutated
Genetic modifications not related to a disease
Isogenic modification
3p25.1
c.1425 G>A
p.Arg475Arg
Homozygous
Silent mutation (Editing strategy; downstream of the pathogenic homozygous nonsense mutation introduced)
Mutated
Isogenic modification
3p25.1
c. 1431 G>A
p.Lys477Lys
Homozygous
Silent mutation (unexpected; downstream of the pathogenic homozygous nonsense mutation introduced)
Mutated
Isogenic modification
3p25.1
c.1437 G>A
p.Gly479Gly
Silent mutation (Editing strategy; downstream of the pathogenic homozygous nonsense mutation introduced)