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UKBi010-A

iLB-DS-95f-r8

iPSC line

Not-for-profit transfer fee: £1400 per vial
No longer available
The cell line was withdrawn.

General#

Cell Line

hPSCreg name UKBi010-A
Alternative name(s)
iLB-DS-95f-r8
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
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Donor's gene variants:
SCN1A
Donor diseases:
Dravet syndrome
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Donor's gene variants:
SCN1A, SCN1A
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Dravet syndrome
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SCN1A
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Dravet syndrome
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SCN1A
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PFIZi017-A
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Donor's gene variants:
SCN1A, SCN1A
Donor diseases:
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PFIZi019-A
(RCi202, BC145c6)
Donor's gene variants:
SCN1A, SCN1A
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PFIZi014-A
(OD002-s7)
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SCN1A
Donor diseases:
Dravet syndrome
PFIZi021-A
(OD001-s7)
Donor's gene variants:
SCN1A
Donor diseases:
Dravet syndrome

Provider

Depositor Universitätsklinikum Bonn (UKB)
Owner Institut für Rekonstruktive Neurobiologie
Distributors
EBiSC
Institut für Rekonstruktive Neurobiologie
Scottish Centre for Regenerative Medicine
Derivation country Germany

External Databases

hPSCreg UKBi010-A
BioSamples SAMEA104008300
Cellosaurus CVCL_IU29
Wikidata Q54990266

General Information

This EBiSC line can be used for:
Yes
Research use: allowed
Clinical use: no
Commercial use: no

Donor Information#

General Donor Information

Sex female
Age of donor (at collection) 5-9

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • SMEI
  • Severe myoclonus epilepsy of infancy
  • Severe myoclonic epilepsy of infancy
Genetic variants
SCN1A (target)
2q13
NM_006920.5:c.323_326dupTGTA
NP_008851.3:p (Ile110ValfsX10)
Frameshift caused by an duplication in exon 2 of the SCN1A gene (c.323_326dupTGTA; p.Ile110ValfsX10)

External Databases (Donor)

BioSamples SAMEA104010737

hIPSC Derivation#

General

Source cell type
Source cell origin
Any portion of the organ that covers that body and consists of a layer of epidermis and a layer of dermis.
Synonyms
  • portion of skin
  • region of skin
  • skin
  • skin region
  • skin zone
show more synonyms
Age of donor (at collection) 5-9

Reprogramming method

Vector type Integrating
Vector Virus (Retrovirus)
Genes
Is the used vector excisable?
No
Absence of reprogramming vector(s)?
Unknown
Reprogramming vectors silenced?
Yes

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

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

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
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?
No

Characterisation#

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vivo teratoma
Morphology
Mesoderm
Ont Id: UBERON_0000926
In vivo teratoma
Morphology
Neuroepithelial Stem Cell
Ont Id: CL_0002259
In vivo teratoma
Morphology

Microbiology / Virus Screening

HIV 1 Negative
HIV 2 Negative
Hepatitis B Negative
Hepatitis C Negative
Mycoplasma Negative

Genotyping#

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
No

Other Genotyping (Cell Line)

Is there genome-wide genotyping or functional data available?
Yes