PUMCHi001-A-1

IPS34-R-17

General

Cell Line

hPSCreg name PUMCHi001-A-1
Cite as:
PUMCHi001-A-1 (RRID:CVCL_YT12)
Alternative name(s)
IPS34-R-17
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
PUMCHi001-A
(IPS-34)
Donor's gene variants:
LMNA
Donor diseases:
familial partial lipodystrophy type 2
UCLi006-A
(LCMD-L302P-UCL01C2)
Donor's gene variants:
LMNA
Donor diseases:
Congenital muscular dystrophy due to LMNA mutation
CMDi001-A
(01016)
Donor's gene variants:
LMNA
Donor diseases:
Congenital muscular dystrophy
CMDi003-A
(01174)
Donor's gene variants:
LMNA
Donor diseases:
Congenital muscular dystrophy
CMDi004-A
(01175)
Donor's gene variants:
LMNA, LMNA
Donor diseases:
Congenital muscular dystrophy
FAMRCi006-B
(LMNA T4)
Donor's gene variants:
LMNA
Donor diseases:
Emery-Dreifuss Muscular Dystrophy
Dilated Cardiomyopathy
FAMRCi005-A
(LMNA B4)
Donor's gene variants:
LMNA
Donor diseases:
myopathy
atrioventricular block
Paroxysmal ventricular tachycardia
FAMRCi005-B
(LMNA B5)
Donor's gene variants:
LMNA
Donor diseases:
myopathy
atrioventricular block
Paroxysmal ventricular tachycardia
FAMRCi006-A
(LMNA T3)
Donor's gene variants:
LMNA
Donor diseases:
Emery-Dreifuss Muscular Dystrophy
Dilated Cardiomyopathy
EHTJUi005-A-3
(ZB11ALD-L4)
Last update 28th May 2020
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Provider

Generator Peking Union Medical College Hospital (PUMCH)
Owner Peking Union Medical College Hospital (PUMCH)
Derivation country China

External Databases

Cellosaurus CVCL_YT12
BioSamples SAMEA7059978
Wikidata Q98128715

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.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • FPLD2
  • familial lipodystrophy of limbs and lower trunk
  • familial partial lipodystrophy Dunnigan type
  • reverse partial lipodystrophy
show more synonyms
Genetic variants
LMNA (target)
NM_170707.4:c.1045C>T
Heterozygous

External Databases (Donor)

BioSamples SAMEA7059977

Ethics

Also have a look at the ethics information for the parental line PUMCHi001-A .
Is there an MTA available for the cell line? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? Shanghai Gemple Biotechnology Co, LTD, China

hIPSC Derivation

General

The source cell information can be found in the parental cell line PUMCHi001-A.

Reprogramming method

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

Vector free reprogramming

Other

Selection criteria for clones manually picked using a 100 μl tip.
Derived under xeno-free conditions
Unknown
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzyme-free cell dissociation
EDTA
O2 Concentration 21 %
CO2 Concentration 5 %
Medium mTeSR™ 1
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line?
Yes

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
NANOG
Yes
SOX2
Yes
POU5F1 (OCT-4)
Yes
TRA 1-60
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
SOX17
Yes
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Marker Expressed
alpha-SMA
Yes
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation
Marker Expressed
Tuj1
Yes

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XY
Passage number: 22
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • FPLD2
  • familial lipodystrophy of limbs and lower trunk
  • familial partial lipodystrophy Dunnigan type
  • reverse partial lipodystrophy
show more synonyms
Genetic modifications
LMNA (target)
Isogenic modification
NM_170707.4:c.1045C>T
Heterozygous
Repaired