RCPCMi007-A-2

FFIS MICA KO 62

The cell line is not validated yet.

General

iPSC Line

hPSCreg name RCPCMi007-A-2
Cite as:
RCPCMi007-A-2
Alternative name(s)
FFIS MICA KO 62
iPSC line type Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines No similar lines found.
Last update 7th September 2026
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Provider

Generator Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
Owner Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
Distributors
Derivation country Russia

External iPSC Databases

BioSamples SAMEA123419500

General iPSC Information

* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: allowed
Commercial use: allowed
Subclone of

iPSC Genetic Modification

Genetic modifications not related to a disease
MICA (target)
Gene knock-out
6p21.33
Knockout of the MICA gene was achieved via electroporation of a plasmid encoding Cas9 and a specific guide RNA targeting the MICA locus. The plasmid also contained a GFP reporter, allowing selection of transfected cells by fluorescence‑activated cell sorting (FACS). GFP‑positive cells were single‑cell sorted and expanded, and clones were subsequently screened for biallelic disruption of the MICA gene.
CRISPR-associated (CRISPR/Cas) System

Donor Information

General Donor Information

Sex female

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

External Databases (Donor)

BioSamples SAMEA8944452

Ethics

Also have a look at the ethics information for the parental line RCPCMi007-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? Evrogen
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

iPSC Derivation

General

The source cell information can be found in the parental cell line RCPCMi007-A.
Passage number reprogrammed 13

Reprogramming method

Vector type Non-integrating
Vector Sendai virus

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

Selection criteria for clones cloning on Tesr1 media for 4-5 passages. the main selection criterion morphology and stable karyotype
Derived under xeno-free conditions
Yes
Derived under GMP?
No
Available as clinical grade?
No

iPSC Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzymatically
TrypLE
O2 Concentration 20 %
CO2 Concentration 5 %
Medium mTeSR™ 1
Has Rock inhibitor (Y27632) been used at passage previously with this iPSC line?
Yes
Has Rock inhibitor (Y27632) been used at cryo previously with this iPSC line?
Yes
Has Rock inhibitor (Y27632) been used at thaw previously with this iPSC line?
Yes

iPSC Characterisation

Analysis of undifferentiated iPSCs
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
DPPA-5
Yes
NANOG
Yes
SOX2
Yes
SSEA-4
Yes
TRA 1-60
Yes
POU5F1 (OCT-4)
Yes
SALL-4
Yes
Marker Present Absent
mCpG
OCT4 X
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Marker Expressed
GATA6
Yes
EOMES-N
Yes
CERT1
Yes
Morphology
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Marker Expressed
HOXB7
Yes
APLNR
Yes
HAND-1
Yes
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Marker Expressed
PAMR1
Yes
PAX6
Yes
HES5
Yes

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (iPSC Line)

Has the iPSC line karyotype been analysed?
Yes
46XX
Passage number: 13
Karyotyping method: G-Banding

Other Genotyping (iPSC Line)