STBCi228-A

SFC368-03-01

iPSC line

At European Collection of Authenticated Cell Cultures (ECACC)
A CLIP contains information about a cell line including any specific third party obligations relating to, for example, licensing obligations or the donor consent which affect the use of the cell line.
A batch specific Certificate of Analysis will be available to download once you receive your EBiSC iPSC line.

General#

Cell Line

hPSCreg Name STBCi228-A
Alternative name(s)
SFC368-03-01
Cell line type Human induced pluripotent stem cell (hiPSC)
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GARS1
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neuropathy
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APOE, APOE
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migraine disorder
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Prolonged QT interval
UKKi007-B
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LRIF1, LRIF1
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Facioscapulohumeral dystrophy
UKKi017-A
(NP0075-8D)
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Hypertrophic cardiomyopathy
UKKi018-A
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KCNH2
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Familial long QT syndrome
UKKi019-A
(NP0081-1A)
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KCNH2
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Familial long QT syndrome
UKKi025-A
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MYH7
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Hypertrophic cardiomyopathy
UKKi018-B
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Familial long QT syndrome
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KCNH2
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Familial long QT syndrome
UKKi019-C
(NP0081-12C)
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KCNH2
Donor diseases:
Familial long QT syndrome
UKKi017-B
(NP0075-10K)
Donor diseases:
Hypertrophic cardiomyopathy
UKKi017-C
(NP0075-11B)
Donor diseases:
Hypertrophic cardiomyopathy
UKKi025-B
(NP0135-2)
Donor's gene variants:
MYH7
Donor diseases:
Hypertrophic cardiomyopathy
UKKi025-C
(NP0135-7)
Donor's gene variants:
MYH7
Donor diseases:
Hypertrophic cardiomyopathy
UKKi018-C
(NP0080-8B)
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KCNH2
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Familial long QT syndrome
CENSOi008-A
(FB77R2c3, CENSOi260)
Donor's gene variants:
DMPK, DMPK
Donor diseases:
myotonic dystrophy type 1
UNEWi004-A
(PRPF31 SH)
Donor's gene variants:
PRPF31
Donor diseases:
Retinitis pigmentosa

Provider

Depositor StemBANCC (STBC)
Distributors
EBiSC
European Collection of Authenticated Cell Cultures (ECACC)

External Databases

hPSCreg STBCi228-A
BioSamples SAMEA104616380
ECACC 66541048
Cellosaurus CVCL_RE98
Wikidata Q54970429
CLO CLO_0104912

General Information

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

Donor Information#

General Donor Information

Sex female

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
neuropathy (primary disease)
Genetic variants

External Databases (Donor)

BioSamples SAMEA104616381

hIPSC Derivation#

General

Source cell type
fibroblast
A connective tissue cell which secretes an extracellular matrix rich in collagen and other macromolecules. Flattened and irregular in outline with branching processes; appear fusiform or spindle-shaped.

Reprogramming method

Vector type Non-integrating
Vector Sendai virus

Vector free reprogramming

Other

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

Culture Conditions#

The following are the depositor culture conditions, they do not refer to any specific batch.
Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzyme-free cell dissociation
EDTA
O2 Concentration 21 %
CO2 Concentration 5 %
Medium mTeSR™ 1

Characterisation#

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR FACS Enzymatic Assay Expression Profiles
Morphology pictures
Morphology post thaw and at passage 10
Differentiation Potency

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping#

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
No abnormalities detected
Karyotyping method: Molecular karyotyping by SNP array
http://

Other Genotyping (Cell Line)