UMGWi004-B-1

BNH1_iPSC_FHS1_cr_well7_JR

The cell line is not validated yet.

General

Cell Line

hPSCreg name UMGWi004-B-1
Cite as:
UMGWi004-B-1
Alternative name(s)
BNH1_iPSC_FHS1_cr_well7_JR
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 15th January 2025
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Provider

Generator Department of Functional Genomics - Human Molecular Genetics (UMGW)
Derivation country Germany

External Databases

BioSamples SAMEA115884924

General Information

* 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 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
All cell lines of this donor's relatives

External Databases (Donor)

BioSamples SAMEA115116692

Ethics

Also have a look at the ethics information for the parental line UMGWi004-B .
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?
Are you aware of any constraints on the use or distribution of the cell line from the owner or any parties identified in the query above? No

hIPSC Derivation

General

The source cell information can be found in the parental cell line UMGWi004-B.

Reprogramming method

Vector type Non-integrating
Vector Episomal
Is reprogramming vector detectable?
No
Methods used
PCR
Notes on reprogramming vector detection PCR for EBNA1 and OriP showed no residual vector in the iPSC
Files and images showing reprogramming vector expressed or silenced

Vector free reprogramming

Other

Selection criteria for clones Sanger sequencing of target gene and analysis of chromatograms with online tools TIDE (http://shinyapps.datacurators.nl/tide/) and indigo (https://www.gear-genomics.com/indigo/)
Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Mechanically
CO2 Concentration 5 %
Medium mTeSR™ 1
Supplements
Penicillin-Streptomycin, 10.000 U/ml Penicillin, 10 mg/ml Pan Biotech 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
SOX2
Yes
POU5F1 (OCT-4)
Yes
NANOG
Yes
TRA 1-60
Yes
Morphology pictures
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
AFP
Yes
SOX17
Yes
Morphology
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Marker Expressed
SMA
Yes
TBXT
Yes
Morphology
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation
Marker Expressed
Tuj1
Yes
PAX6
Yes
Morphology

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46/XY
Passage number: 13
Karyotyping method: low-coverage whole genome sequencing (lcWGS)

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • FLHS
Genetic modifications
SRCAP (target)
Isogenic modification
16p11.2
NM_006662.3:c.7301_7302insA
NM_006662.3:p.(Arg2435Alafs*8)
Heterozygous
Target region was analysed by PCR and Sanger sequencing. Heterozygous state was proven by comparing the chromatogram to the wildtype and reference genome GRCh38, using the Tools TIDE (https://tide.nki.nl/) and indigo (https://www.gear-genomics.com/indigo/). Mutation was predicted as pathogenic by MutationTaster (https://www.mutationtaster.org/).
Mutated