MHHi001-A-20

cyclinB1-eGFP hiPSCs

The cell line is not validated yet.

General

Cell Line

hPSCreg name MHHi001-A-20
Cite as:
MHHi001-A-20
Alternative name(s)
cyclinB1-eGFP hiPSCs
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 3rd February 2025
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Provider

Generator Hannover Medical School (MHH)
Owner Hannover Medical School (MHH)
Distributors
Derivation country Germany

External Databases

BioSamples SAMEA117736335

General Information

* Is the cell line readily obtainable for third parties?
Yes
Cell line can only be used in: we are happy to provide the cell line using an official Material Transfer Agreement for research use only.
Research use: allowed
Subclone of

Donor Information

General Donor Information

Sex female
Ethnicity Caucasian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Family history N/A
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

External Databases (Donor)

BioSamples SAMEA4564585

Ethics

Also have a look at the ethics information for the parental line MHHi001-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 MHHi001-A.

Reprogramming method

Vector type None

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

Derived under xeno-free conditions
Yes
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 37 %
CO2 Concentration 5 %
Medium Essential 8™

Characterisation

Analysis of Undifferentiated Cells
Marker Present Absent
mCpG
OCT4 X
Self-renewal
Unknown
Endoderm
Positive
Mesoderm
Positive
Ectoderm score
Positive
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Cardiac Muscle Cell
Ont Id: CL_0000746
In vitro directed differentiation
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XX
Passage number: 19
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Genetic modifications not related to a disease
Transgene expression
We used cyclinB1-eGFP lentivirus particles. EGFP positive cells were isolated by fluorescence-activated cell sorting (FACS), re-sorted and replated as the founder polyclonal reporter line.
Viral
Lentivirus
cvae175.pdf
Original research article describing the cell line