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WTSIi190-B

HPSI0914i-kajh_2

iPSC line

Not-for-profit fee: £1400 per vial
Stock not immediately available - enquire for details
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General#

Cell Line

hPSCreg name WTSIi190-B
Alternative name(s)
HPSI0914i-kajh_2
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
WTSIi190-A
(HPSI0914i-kajh_3)

Provider

Depositor Wellcome Sanger Institute (WTSI)
Distributors
EBiSC
Derivation country United Kingdom

External Databases

hPSCreg WTSIi190-B
BioSamples SAMEA3853122
HipSci HPSI0914i-kajh_2
Cellosaurus CVCL_EE69
Wikidata Q54891505

General Information

Publications View all related publications on hPSCreg (1)
This EBiSC line can be used for:
Yes
Research use: allowed
Clinical use: no
Commercial use: no

Donor Information#

General Donor Information

Sex female
Age of donor (at collection) 60-64
Ethnicity White - White British

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.

Donor Relations

Other cell lines of this donor

External Databases (Donor)

BioSamples SAMEA2784660
HipSci HPSI-kajh

hIPSC Derivation#

General

Source cell type
A connective tissue cell which secretes an extracellular matrix rich in collagen and other macromolecules. Flattened and irregular in outline with branching processes; appear fusiform or spindle-shaped.; These cells may be vimentin-positive, fibronectin-positive, fsp1-positive, MMP-1-positive, collagen I-positive, collagen III-positive, and alpha-SMA-negative.
Source cell origin
Any portion of the organ that covers that body and consists of a layer of epidermis and a layer of dermis.
Synonyms
  • portion of skin
  • region of skin
  • skin
  • skin region
  • skin zone
show more synonyms
Age of donor (at collection) 60-64
Collected in 2015
Source cell line vendor Cambridge BioResource

Reprogramming method

Vector type Non-integrating
Vector Sendai virus
Genes
Notes on reprogramming vector detection CytoTune 2

Vector free reprogramming

Other

Selection criteria for clones Morphology
Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions#

The following are the depositor culture conditions, they do not refer to any specific batch.
Surface coating Vitronectin
Feeder cells
No
Passage method Enzyme-free cell dissociation
EDTA
CO2 Concentration 5 %
Medium TeSR™ E8™

Characterisation#

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
POU5F1 (OCT-4)
Yes
SOX2
Yes
NANOG
Yes
Pluripotency Score Novelty Score
31.199 1.219

Genotyping#

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
No

Other Genotyping (Cell Line)

Is there genome-wide genotyping or functional data available?
Yes
Exome sequencing
cnv
http://www.hipsci.org/lines/#/lines/HPSI0914i-kajh_2
Number of regions different from primary tissue: 0; Length of differences from primary tissue: 0
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860633
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860537
Raw sequencing reads
RNA-seq
http://www.ebi.ac.uk/ena/data/view/ERR1629747
Raw sequencing reads
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERZ376637
Imputed and phased genotypes
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERZ376461
BWA alignment
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860057
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1861017
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1859961
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1861113
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERZ448095
GATK haplotype calls
Genotyping array
http://www.ebi.ac.uk/ena/data/view/ERZ369189
Genotyping array calls
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1560605
Raw sequencing reads
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1560523
Raw sequencing reads
Methylation profiling
http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4059/
Text file with probe intensities
RNA-seq
http://www.ebi.ac.uk/ena/data/view/ERZ376110
Abundances of transcripts
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860729
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860825
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860921
Raw sequencing reads
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1560589
Raw sequencing reads
Exome sequencing
http://www.ebi.ac.uk/ena/data/view/ERZ376813
mpileup variant calls
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1860441
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1861209
Raw sequencing reads
Whole genome sequencing
http://www.ebi.ac.uk/ena/data/view/ERR1861305
Raw sequencing reads
Genotyping array
http://www.ebi.ac.uk/ena/data/view/ERZ368897
Genotyping array calls
RNA-seq
http://www.ebi.ac.uk/ena/data/view/ERR1629738
Raw sequencing reads
RNA-seq
http://www.ebi.ac.uk/ena/data/view/ERZ376251
Splice-aware STAR alignment
WGS-derived disease associations
autosomal recessive nonsyndromic hearing loss 63 (LRTOMT)
Brugada syndrome 1 (CACNB2)
Charcot-Marie-Tooth disease (FIG4)
Cohen syndrome (VPS13B)
complex neurodevelopmental disorder (CNTNAP2, SETBP1)
dilated cardiomyopathy (NPPA)
familial ovarian cancer (GEN1)
Fanconi anemia complementation group A (FANCA)
focal segmental glomerulosclerosis 9 (CRB2)
hereditary breast carcinoma (GEN1)
hypertrophic cardiomyopathy (CACNB2)
microcephaly, seizures, and developmental delay (PNKP)
mitochondrial disease (NDUFS6)
myopathy caused by variation in POMT1 (POMT1)
nonsyndromic genetic hearing loss (MYO7A)
PHARC syndrome (ABHD12)
primary ciliary dyskinesia 7 (DNAH11)
PTEN hamartoma tumor syndrome (PTEN)
pyridoxine-dependent epilepsy (ALDH7A1)
Rothmund-Thomson syndrome (RECQL4)
Schinzel-Giedion syndrome (SETBP1)
short QT syndrome (CACNB2)
Smith-Magenis syndrome (RAI1)
syndromic intellectual disability (KMT2C)
turnpenny-fry syndrome (PCGF2)
Usher syndrome type 1 (MYO7A)
vitamin K-dependent clotting factors, combined deficiency of, type 2 (VKORC1)
X-linked complex neurodevelopmental disorder (SHROOM4)
Other WGS-derived genes
AGL, ALDH3A2, AMPD1, ANAPC1, AURKC, CASP12, CATSPER2, CFC1, CFHR2, CHST15, CLDN16, CNOT1, CYP21A2, D2HGDH, DEFB126, DNAAF1, DSC3, DUSP6, ERCC6L2, FBXO7, FZD6, GALNT3, GDPD4, GPRIN1, IDO2, IL12RB1, INMT, IRF5, ITGB2, KAT2A, KCNJ16, KISS1, LAMA5, MAPT, MED15, MROH8, MTTP, NBPF1, NDUFB9, NFU1, OAS1, OPRM1, OR51F1, OR52B4, P2RX5, PDE4DIP, PIGN, POLDIP2, POLR3B, PTCHD3, PYGL, SCAPER, SLC37A4, SYNE2, TAP2, TBP, TDG, TIGD6, TMEM107, TMEM216, TMPRSS6, TNRC18, TOR1AIP1, TREH, VDR, WDR37, ZAN, ZNF141, ZNF527, ZXDA