RCi172, RCFB60c2

General

Cell Line

hPSCreg name UCLi004-C
Cite as:
UCLi004-C (RRID:CVCL_II90)
Alternative name(s)
RCi172, RCFB60c2
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
UCLi004-A
(RCi173, RCFB60c6)
Donor's gene variants:
C9orf72, C9orf72
Donor diseases:
Amyotrophic lateral sclerosis
Frontotemporal dementia
UCLi004-B
(RCFB60c7, RCi177)
Donor's gene variants:
C9orf72, C9orf72
Donor diseases:
Amyotrophic lateral sclerosis
Frontotemporal dementia
UCLi001-A
(HHItC9S-V19)
Donor's gene variants:
C9orf72
Donor diseases:
Frontotemporal dementia
UCLi002-A
(HHItC9D-V34, DN19)
Donor's gene variants:
C9orf72, C9orf72
Donor diseases:
Frontotemporal dementia
UEFi010-A
(FTD3)
Donor's gene variants:
C9orf72
Donor diseases:
Behavioral variant of frontotemporal dementia
UEFi013-A
(FTD6)
Donor's gene variants:
C9orf72
Donor diseases:
Behavioral variant of frontotemporal dementia
UEFi012-A
(FTD5)
Donor's gene variants:
C9orf72
Donor diseases:
Behavioral variant of frontotemporal dementia
LUBi001-A
(PGRN-8310, PGRN8310, RCi195, RCFB58 c12.5)
Donor's gene variants:
GRN, GRN, GRN, GRN
Donor diseases:
Frontotemporal dementia
CBIGi022-A-1
(SOD1 I114T correction (CBIGi022-A), IPSC0029)
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
LUBi001-B
(PGRN-8310, RCFB58 c4.4, PGRN8310, RCi194)
Donor's gene variants:
GRN, GRN, GRN, GRN
Donor diseases:
Frontotemporal dementia
LUBi001-C
(PGRN-8310, RCFB58 c3.7, RCi200, PGRN8310)
Donor's gene variants:
GRN, GRN, GRN, GRN
Donor diseases:
Frontotemporal dementia
UHi002-A
(HEL13.1, ALS50)
Donor diseases:
obsolete_amyotrophic lateral sclerosis
UHi003-A
(ALS75, HEL15.14)
Donor diseases:
obsolete_amyotrophic lateral sclerosis
UCLi009-A
(CB1D)
Donor's gene variants:
VCP
Donor diseases:
Frontotemporal dementia
PFIZi013-A
(RCi215, RCFB59 C9)
Donor's gene variants:
TARDBP, TARDBP
Donor diseases:
Amyotrophic lateral sclerosis
HVRDi009-A
(29e SOD1 L144F, 29e)
Donor diseases:
obsolete_amyotrophic lateral sclerosis
UCLi003-A
(TSM(exon10+16)V97)
Donor's gene variants:
MAPT
Donor diseases:
Frontotemporal dementia
UCLi010-A
Donor's gene variants:
VCP
Donor diseases:
Frontotemporal dementia
UCLi010-B
(GL1B)
Donor's gene variants:
VCP
Donor diseases:
Frontotemporal dementia
CBIGi038-A
(IPSC0049)
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi043-A
(IPSC0057)
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi047-A
(IPSC0091)
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi048-A
(IPSC0092)
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi049-A
(IPSC0093, SOD1 I144T(CBIGi049-A))
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
MNDi002-A
(MND-Nek1-P002)
Donor diseases:
Amyotrophic Lateral Sclerosis
MNDi004-A
(MND-Nek1-P004)
Donor diseases:
Amyotrophic Lateral Sclerosis
MNDi005-A
(MND-Nek1/C9-P001)
Donor diseases:
Amyotrophic Lateral Sclerosis
NIMHi008-A
(NphyiALS1)
Donor's gene variants:
LDB3
Donor diseases:
Amyotrophic Lateral Sclerosis
UCSCi001-A
(SII-1802)
Donor diseases:
Amyotrophic Lateral Sclerosis
SAPi003-A
(ALS II, FUS-R521C/wt, ALS II–FUS-R521C/wt)
Donor diseases:
Amyotrophic lateral sclerosis
SAPi004-A
(ALS III, TDP43-A382T/A382T, ALS III-TDP43-A382T/A382T)
Donor diseases:
Amyotrophic lateral sclerosis
CSSi012-A
Donor's gene variants:
TARDBP
Donor diseases:
Amyotrophic lateral sclerosis
CBIGi022-A
(IPSC0028, SOD1 I114T (CBIGi022-A))
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi023-A
(IPSC0030, sporadic sALS+FTD)
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi024-A
(IPSC0031, SOD1 I144T (CBIGi024-A))
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi025-A
(IPSC0032)
Donor diseases:
Amyotrophic Lateral Sclerosis
UCLi009-B
(CB1E)
Donor's gene variants:
VCP
Donor diseases:
Frontotemporal dementia
CBIGi010-A
(SOD1 A4S, IPSC0014)
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi011-A
(SOD1 I114T, IPSC0015)
Donor's gene variants:
SOD1, SOD1
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi014-A
(VAPB A2V, IPSC0019)
Donor's gene variants:
VAPB, VAPB
Donor diseases:
Amyotrophic Lateral Sclerosis
CBIGi020-A
(IPSC0026)
Donor diseases:
Amyotrophic Lateral Sclerosis
Last update 3rd July 2019
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Provider

Generator University College London (UCL)
Distributors

External Databases

BioSamples SAMEA4085372
Cellosaurus CVCL_II90
Wikidata Q54989672

General Information

Projects
* 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 male
Age of donor (at collection) 50-54

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • Lou Gehrig disease
  • Charcot disease
  • ALS
Genetic variants
C9orf72 (target)
9p21.2
C9orf72 hexanucleotide expansion.
The donor was not diagnosed with FTD at the time of sample collection. FTD is listed due to the association with C9ORF72.
Synonyms
  • FTD
Genetic variants
C9ORF72 hexanucleotide repeat expansion

Donor Relations

Other cell lines of this donor

External Databases (Donor)

BioSamples SAMEA3964276

Ethics

Has informed consent been obtained from the donor of the embryo/tissue from which the pluripotent stem cells have been derived? Yes
Was the consent voluntarily given? Yes
Has the donor been informed that participation will not directly influence their personal treatment? No
Can you provide us with a copy of the Donor Information Sheet provided to the donor? Yes
Do you (Depositor/Provider) hold the original Donor Consent Form? No
If you do not hold the Donor Consent Form, do you know who does? Yes
Is there other documentation provided to the donor for consenting purposes? Yes
Confirm that consent was obtained by a qualified professional Yes
Has the donor agreed to be re-contacted? No
Has the donor been informed about how her/his data will be protected? Yes
Please indicate whether the data associated with the donated material has been pseudonymised or anonymised. pseudonymised
Does consent explicitly allow the derivation of pluripotent stem cells? Yes
* Does consent expressly prevent the derivation of pluripotent stem cells? No
* Does consent pertain to a specific research project? No
Does consent permit unforeseen future research, without further consent? Yes
Does the consent permit uses of donated embryo/tissue or derived cell line intended for clinical treatment or human applications? No
Does consent expressly prevent development of commercial products? No
Does consent expressly prevent financial gain from any use of the donated embryo/tissue, including any product made from it? No
Does consent expressly permit storage of donated embryo/tissue for an unlimited time? Yes
Does consent prevent the DONATED BIOSAMPLE from being made available to researchers anywhere in the world? No
Does consent prevent CELLS DERIVED FROM THE DONATED BIOSAMPLE from being made available to researchers anywhere in the world? No

Does consent permit research by

an academic institution? Yes
a public organisation? Yes
a non-profit company? Yes
a for-profit corporation? Yes
Does consent expressly permit collection of genetic information? Yes
Has the donor been informed that their donated biosample or derived cells may be tested for the presence of microbiological agents / pathogens? Yes
How may genetic information associated with the cell line be accessed? Open Access
Will the donor expect to receive financial benefit, beyond reasonable expenses, in return for donating the biosample? No
Does the consent permit the donor, upon withdrawal of consent, to stop the use of the derived cell line(s) that have already been created from donated samples? No
Does the consent permit the donor, upon withdrawal of consent, to stop delivery or use of information and data about the donor? No
Does consent permit access to medical records of the donor? No
Does consent permit access to any other source of information about the clinical treatment or health of the donor? No
Has a favourable opinion been obtained from a research ethics committee, or other ethics review panel, in relation to the Research Protocol including the consent provisions? Yes
Name of accrediting authority involved? Institute of Neurology Joint Research Ethics Committee
Approval number 09/H0716/64
Has a favourable opinion been obtained from a research ethics committee, or other ethics review panel, in relation to the PROPOSED PROJECT, involving use of donated embryo/tissue or derived cells? Yes
Name of accrediting authority involved? Institute of Neurology Joint Research Ethics Committee
Approval number 09/H0716/64
Do you have obligations to third parties in regard to the use of the cell line? No
Are you aware of any further constraints on the use of the donated embryo/tissue or derived cells? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General

Source cell type
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.; These cells may be vimentin-positive, fibronectin-positive, fsp1-positive, MMP-1-positive, collagen I-positive, collagen III-positive, and alpha-SMA-negative.
Age of donor (at collection) 50-54

Reprogramming method

Vector type Non-integrating
Vector Sendai virus
Genes

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

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 Essential 8™

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
SSEA-1
No
SSEA-4
Yes
TRA 1-60
Yes
POU5F1 (OCT-4)
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation

Microbiology / Virus Screening

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

Certificate of Analysis

Is there a certificate of analysis available?
Yes
Passage: 22

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
No autosomal or sex chromosome aneuplodies detected
Passage number: 22
Karyotyping method: Karyolite BoBs

Other Genotyping (Cell Line)