STBCi017-A-1

SCN9A: Correction of loss of function mutation

The cell line is not submitted yet.
(only basic data is shown)

General

Cell Line

hPSCreg name STBCi017-A-1
Cite as:
STBCi017-A-1 (RRID:CVCL_C1WW)
Alternative name(s)
SCN9A: Correction of loss of function mutation
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 28th July 2022
User feedback
No feedback available yet.

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

Provider

Generator AstraZeneca AB (AZ)

External Databases

Cellosaurus CVCL_C1WW
Wikidata Q114313047

General Information

Subclone of

hIPSC Derivation

General

The source cell information can be found in the parental cell line STBCi017-A.