AHQUi001-A-1

IPS35-2-R

General

Cell Line

hPSCreg Name
AHQUi001-A-1
Alternative name(s)
IPS35-2-R
Cell line type Human induced pluripotent stem cell (hiPSC)
Last update 12th February 2021
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Provider

Generator Affiliated Hospital of Qingdao University (AHQU)

External Databases

BioSamples SAMEA7655488
Cellosaurus CVCL_A1MV
Wikidata Q102113510
CLO CLO_0103635

General Information

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

Donor Information

General Donor Information

Sex male
Ethnicity Chinese Han

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
NON RARE IN EUROPE: Hyperlipoproteinemia type 4
Familial hypertriglyceridemia (FHTG)
The donor is a carrier of a disease-associated mutation.
Synonyms
  • Familial hypertriglyceridemia
  • HLP type 4
Genetic variants
LPL (target)
NM_000237.3:c.928 T>C
p.C310R
Heterozygous

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 SAMEA6516985

Ethics

Also have a look at the ethics information for the parental line AHQUi001-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 AHQUi001-A.

Reprogramming method

Vector type Non-integrating
Vector Episomal
Genes
Is reprogramming vector detectable?
No
Methods used
PCR

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
Passage method Enzyme-free cell dissociation
EDTA
CO2 Concentration 5 %
Medium mTeSR™ 1

Characterisation

No characterisation data could be found for this subclone. Please open parental cell line AHQUi001-A .

Genotyping

Karyotyping (Cell Line)

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
hyperlipoproteinemia type IV
Familial hypertriglyceridemia (FHTG)
Genetic modifications
LPL (target)
Isogenic modification
NM_000237.3:c.928 T>C
p.C310R
Heterozygous
Repaired