CEBe033-A-1

GBA1_hESC_GBA#1-/-_10.18.11

General

Cell Line

hPSCreg name CEBe033-A-1
Cite as:
CEBe033-A-1 (RRID:CVCL_QX50)
Alternative name(s)
GBA1_hESC_GBA#1-/-_10.18.11
Cell line type Human embryonic stem cell (hESC)
Similar lines
CEBe033-A
(SA001)
CEBe033-A-11
(SA001_WT_HGPRT_2)
CEBe033-A-8
(SA001_KO_HGPRT_1)
CEBe033-A-9
(SA001_KO_HGPRT_2)
CEBe033-A-10
(SA001_WT_HGPRT_1)
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)
Last update 22nd May 2019
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Provider

Generator F. Hoffmann-La Roche Ltd (ROCHE)
Owner F. Hoffmann-La Roche Ltd (ROCHE)

External Databases

BioSamples SAMEA104132790
Cellosaurus CVCL_QX50
Wikidata Q54809126

General Information

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

Donor Information

General Donor Information

Sex male

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Karyotyping (Donor)

Has the donor karyotype been analysed?
Yes
X,Y 46
Karyotyping method: G-Banding

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 .
Was the embryo established purely for research purposes? Yes
Have both parents consented to the use of the embryo for ESC derivation? Yes
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
Alternatives to consent are available? Yes
Alternatives to consent
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
Will the donor expect to receive financial benefit, beyond reasonable expenses, in return for donating the biosample? 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? EKBB Ethikkommisson beider Basel Hebelstrasse 53 4056 Basel
Approval number R-FP-S-2-0006-0006

hESC Derivation

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

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzymatically
Accutase
O2 Concentration 19 %
CO2 Concentration 5 %
Medium mTeSR™ 1
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?
Yes
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
NANOG
Yes
POU5F1 (OCT-4)
Yes
Differentiation Potency
Neuron
Ont Id: CL_0000540
Neuroepithelial Stem Cell
Ont Id: CL_0002259

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
X,Y, 46

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
targeted insertion of disruption cassettes (pGK-neo, pGK-puro) into exon 4 of both alleles
Synonyms
  • Glucocerebrosidase deficiency
  • Acid beta-glucosidase deficiency
Genetic modifications
GBA (target)
Gene knock-in
1q22
1q22
Zinc finger nuclease