SKLRMi001-A-1

AR repaired iPSCs

General

Cell Line

hPSCreg name SKLRMi001-A-1
Cite as:
SKLRMi001-A-1 (RRID:CVCL_D0LQ)
Alternative name(s)
AR repaired iPSCs
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
Last update 15th February 2023
User feedback
No feedback available yet.

Login to share your feedback, experiences or results with the research community.

Provider

Generator State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
Owner State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
Distributors
Derivation country China

External Databases

BioSamples SAMEA112648452
Cellosaurus CVCL_D0LQ
Wikidata Q123033516

General Information

Publications
* Is the cell line readily obtainable for third parties?
No
Subclone of

Donor Information

General Donor Information

Sex male

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
Synonyms
  • Goldberg-Maxwell syndrome
  • Testicular feminization syndrome
  • Androgen resistance syndrome
  • AIS
  • Morris syndrome
show more synonyms

External Databases (Donor)

BioSamples SAMEA6649976

Ethics

Also have a look at the ethics information for the parental line SKLRMi001-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 SKLRMi001-A.

Reprogramming method

Vector type Non-integrating
Vector Episomal

Vector free reprogramming

Other

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

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Medium Essential 8™

Characterisation

No characterisation data could be found for this subclone. Please open parental cell line SKLRMi001-A .

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
normal karyotype

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Genetic modifications
AR (target)
Isogenic modification
Xq12
NM_000044.6:c.2710G>A
NP_000035.2:p.V904M
Repaired
Genetic modifications not related to a disease
AR (target)
Isogenic modification
Xq12
NM_000044.6:c.2710G>A
NP_000035.2:p.V904M
Repaired