WAe001-A-65

General#

Cell Line

hPSCreg Name WAe001-A-65
Cell line type Human embryonic stem cell (hESC)
Last update 19th February 2021
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Provider

Generator Nanfang Hospital, Southern Medical University (NFYY)

External Databases

BioSamples SAMEA8268467

General Information

* Is the cell line readily obtainable for third parties?
Yes
Research: allowed
Clinical: not allowed
Commercial: not allowed
Subclone of

Donor Information#

General Donor Information

Sex male

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

Donor Relations

Other cell lines of this donor

External Databases (Donor)

BioSamples SAMEA7767418

Ethics#

Also have a look at the ethics information for the parental line WAe001-A .

hESC Derivation#

Date of derivation 2019-12-12
Supernumerary embryos from IVF treatment?
Yes
Separation of research and IVF treatment?
Yes
PGD Embryo?
No

Culture Conditions#

Medium mTeSR™ 1

Characterisation#

No characterisation data could be found for this subclone. Please open parental cell line WAe001-A

Genotyping#

Karyotyping (Cell Line)

Other Genotyping (Cell Line)

Genetic Modification#

Disease/phenotype related modifications
Epileptic encephalopathy
Homozygous varian in the BAF53B (ACTL6B) gene leads to Epileptic Encephalopathy.
Synonyms
  • Convulsive encephalopathy
Genetic modifications
BAF53B (target)
Variant
7q22.1
Homozygous
Genetic modifications not related to a disease
BAF53B (target)
Gene knock-out
7q22.1
BAF53B homozygous knockout.
CRISPR-associated (CRISPR/Cas) System