CBCHi001-A-1

The cell line is not validated yet.

General

Cell Line

hPSCreg name CBCHi001-A-1
Cite as:
CBCHi001-A-1 (RRID:CVCL_C1SU)
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
ICANi001-A-1
(CDGEN1.16.40.5)
Donor diseases:
hypertrophic cardiomyopathy
UKEi070-A-1
(Rep 28, Iso Co)
Donor diseases:
hypertrophic cardiomyopathy
UKEi070-A-2
(Bi-allelic mutant, Mut 103)
Donor diseases:
hypertrophic cardiomyopathy
NUIGi038-B-1
(CR.LQTH002Cx-A17)
NUIGi038-B-2
(CR.LQTH002Cx-A21)
NUIGi038-B-3
(CR.LQTH002Cx-3A15)
NUIGi038-B-4
(CR.LQTH002Cx-3A18)
Last update 1st April 2022
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Provider

Generator Beijing Chest Hospital (CBCH)

External Databases

BioSamples SAMEA13855333
Cellosaurus CVCL_C1SU
Wikidata Q114310765

General Information

* 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 female

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

External Databases (Donor)

BioSamples SAMEA13855308

Ethics

Also have a look at the ethics information for the parental line CBCHi001-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 CBCHi001-A.

Reprogramming method

Vector type Non-integrating
Vector Sendai virus

Vector free reprogramming

Other

Derived under xeno-free conditions
Unknown
Derived under GMP?
Unknown
Available as clinical grade?
Unknown

Culture Conditions

Medium mTeSR™ Plus

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
SOX2
Yes
SSEA-4
Yes
Score:
Marker Present Absent
mCpG
OCT4
Differentiation Potency

Genotyping

Karyotyping (Cell Line)

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • Hypertrophic Cardiomyopathy
Genetic modifications
Variant
15q14
NM_005159.5:c.715G>C