K7-4Lf MT21
ICGi022-A-9
General
Cell Line |
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hPSCreg name | ICGi022-A-9 |
Cite as: | ICGi022-A-9 |
Alternative name(s) |
K7-4Lf MT21
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines | No similar lines found. |
Last update | 3rd December 2024 |
User feedback | |
Provider |
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Generator | Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG) |
Owner | Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG) |
Distributors | |
Derivation country | Russia |
External Databases |
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BioSamples | SAMEA117402930 |
General Information |
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* Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
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Subclone of |
Donor Information
General Donor Information |
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Sex | female |
Ethnicity | Caucasian |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Other Genotyping (Donor) |
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Is there genome-wide genotyping or functional data available? |
Yes
Exome sequencing
https://www.ncbi.nlm.nih.gov/sra/?term=SRR11413027 No disease associated mutation found |
Donor Relations |
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Other cell lines of this donor | |
External Databases (Donor) |
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BioSamples | SAMN14446266 |
Ethics
Also have a look at the ethics information for the parental line
ICGi022-A
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For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? |
hIPSC Derivation
General |
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The source cell information can be found in the parental cell line
ICGi022-A.
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Reprogramming method |
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Vector type | Non-integrating |
Vector | Episomal |
Is reprogramming vector detectable? |
No |
Methods used |
PCR
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Vector free reprogramming |
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Type of used vector free reprogramming factor(s) |
None
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Other |
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Derived under xeno-free conditions |
No |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Gelatin | ||||||||||||||||||
Feeder cells |
Mouse embryonic fibroblasts Cellfinder Ont Id: EFO_0004040 |
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Passage method |
Enzymatically
TrypLE
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O2 Concentration | 20 % | ||||||||||||||||||
CO2 Concentration | 5 % | ||||||||||||||||||
Medium |
Other medium:
Base medium: KnockOut DMEM
Main protein source: Knock-out serum replacement Serum concentration: 15 % Supplements
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Has Rock inhibitor (Y27632) been used at passage previously with this cell line? | Yes |
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Has Rock inhibitor (Y27632) been used at cryo previously with this cell line? | No |
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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 |
POU5F1 (OCT-4) |
Yes |
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SSEA-4 |
Yes |
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SOX2 |
Yes |
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NANOG |
Yes |
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TRA 1-60 |
Yes |
Differentiation Potency
In vitro spontaneous differentiation
Marker | Expressed |
CD29 |
Yes |
Actin, alpha 2, smooth muscle, aorta |
Yes |
Microbiology / Virus Screening |
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Mycoplasma | Negative |
Genotyping
Karyotyping (Cell Line) |
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Has the cell line karyotype been analysed? |
Yes
Karyotyping and G-banding show ICGi022-A-9 iPSCs have a normal 46,XX karyotype at passage 10.
Passage number: 10
Karyotyping method:
G-Banding
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Other Genotyping (Cell Line) |
Genetic Modification
Genetic modifications not related to a disease |
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