ICGi021-A-3

K6-4fpCyto-19

General

Cell Line

hPSCreg name ICGi021-A-3
Cite as:
ICGi021-A-3
Alternative name(s)
K6-4fpCyto-19
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
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(K6-4fpCyto-13)
ICGi021-A-2
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ICGi015-B-3
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ICGi034-A-1
(PD30-XBP-RFP-6, PD30-4-7-XBP-RFP-6)
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ICGi034-A-2
(PD30-4-7-XBP-RFP-51, PD30-XBP-RFP-51)
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ICGi034-A-3
(PD30-4-7-XBP-RFP-52, PD30-XBP-RFP-52)
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ICGi034-A-4
(PD30-4-7-XBP-RFP-86, PD30-XBP-RFP-86)
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obsolete_Parkinson's disease
Last update 18th June 2021
Notes Healthy human iPSC clone with doxycycline-inducible expression of cytosolic Grx1-roGFP2
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Provider

Generator Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
Derivation country Russia

External Databases

BioSamples SAMEA9232931

General Information

* Is the cell line readily obtainable for third parties?
Yes
Cell line can only be used in: Any
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Subclone of

Donor Information

General Donor Information

Sex female
Ethnicity Caucasian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
Yes
Exome sequencing
https://www.ncbi.nlm.nih.gov/sra/?term=SRR11413028
No disease associated mutation found

External Databases (Donor)

BioSamples SAMEA6983569

Ethics

Also have a look at the ethics information for the parental line ICGi021-A .
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General

The source cell information can be found in the parental cell line ICGi021-A.

Reprogramming method

Vector type Non-integrating
Vector Episomal
Is reprogramming vector detectable?
No
Methods used
PCR
Files and images showing reprogramming vector expressed or silenced

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 Gelatin
Feeder cells MEF cell
Cellfinder Ont Id: http://www.ebi.ac.uk/efo/EFO_0004040
Passage method Enzymatically
TrypLE
O2 Concentration 20 %
CO2 Concentration 5 %
Medium Other medium:
Base medium: Knock-out DMEM
Main protein source: Knock-out serum replacement
Serum concentration: 15 %
Supplements
GlutaMAX 2 mM
NEAA 0.1 mM
Penicillin-Streptomycin 100 U/ml
2-mercaptoethanol 0.1 mM
rhFGF basic 10 ng/ml
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?
No
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
SSEA-4
Yes
Alkaline Phosphatase
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
CK-18
Yes
GATA6
Yes
Morphology
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Marker Expressed
aSMA
Yes
Collagen type I
Yes
Morphology
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation
In vitro directed differentiation
Marker Expressed
Tubulin, beta 3
Yes
Neurofilament 200
Yes
Morphology

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

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

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • Healthy
  • Well
Genetic modifications
Genetic modifications not related to a disease
AAVS1 (target)
Transgene expression
19q13
Transgenes of glutathione redox sensor (cytosolic) cyto_Grx1-roGFP2 and tetracycline-transactivator (rtTA) in AAVS1 locus were detected by PCR.
CRISPR-associated (CRISPR/Cas) System
puro in.TIF
CytoGrx1-roGFP2 transgene detection
neo in.TIF
rtTA transgene detection