The EBiSC team is working hard to implement improvements in how EBiSC operates.
Due to some short-term disruption, please get in touch via
Contact@EBiSC.org if
the cells you would like to access are currently listed as unavailable or you
are ordering from outside of Europe.
WTSIi103-A
HPSI1213i-nusw_2
iPSC line
We are currently making some changes to how EBiSC operates and because
of this there is a short period of time where orders cannot be placed.
If you are interested in accessing these cells, please contact EBiSC directly. For more information about the current transition process see here.
If you are interested in accessing these cells, please contact EBiSC directly. For more information about the current transition process see here.
The cell line was withdrawn.
General#
Cell Line |
|
hPSCreg name | WTSIi103-A |
Alternative name(s) |
HPSI1213i-nusw_2
|
Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines | No similar lines found. |
Provider |
|
Depositor | Wellcome Sanger Institute (WTSI) |
Distributors |
EBiSC
|
Derivation country | United Kingdom |
External Databases |
|
hPSCreg | WTSIi103-A |
BioSamples | SAMEA2464779 |
HipSci | HPSI1213i-nusw_2 |
Cellosaurus | CVCL_AI20 |
Wikidata | Q54891724 |
General Information |
|
Publications | View all related publications on hPSCreg (2) |
This EBiSC line can be used for: |
Yes
Research use: allowed
Clinical use: no
Commercial use: no
|
Donor Information#
General Donor Information |
|
Sex | male |
Age of donor (at collection) | 65-69 |
Ethnicity | White - White British |
Phenotype and Disease related information (Donor) |
|
Diseases | No disease was diagnosed.
|
External Databases (Donor) |
|
BioSamples | SAMEA2398815 |
HipSci | HPSI-nusw |
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
|
Age of donor (at collection) | 65-69 |
Collected in | 2014 |
Source cell line vendor | Cambridge BioResource |
Reprogramming method |
|
Vector type | Non-integrating |
Vector | Sendai virus |
Genes | |
Notes on reprogramming vector detection | CytoTune 1 |
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 | Gelatin |
Feeder cells |
Mouse embryo fibroblast (MEF) feeder cells |
Passage method |
Enzymatically
Collagenase and Dispase
|
CO2 Concentration | 5 % |
Medium |
Other medium:
Base medium:
Main protein source: Knock-out serum replacement |
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 | Link to microarray data |
35.818 | 1.861 | http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4057/ |
Report
HPSI-nusw.pluritest.pluripotency_score.20161010.png
pluripotency image
HPSI-nusw.pluritest.novelty_score.20161010.png
novelty image
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
http://www.ebi.ac.uk/ena/data/view/ERZ122995
cnv
http://www.hipsci.org/lines/#/lines/HPSI1213i-nusw_2 Number of regions different from primary tissue: 1; Length of differences from primary tissue: 4
Methylation profiling
http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4059/ Text file with probe intensities |
WGS-derived disease associations |
3-hydroxyisobutyryl-CoA hydrolase deficiency (HIBCH)
Bernard-Soulier syndrome (GP1BA)
Brugada syndrome 1 (CACNB2)
Charcot-Marie-Tooth disease (FIG4)
Cohen syndrome (VPS13B)
complex neurodevelopmental disorder (CNTNAP2, SETBP1)
demyelinating hereditary motor and sensory neuropathy (MTMR2)
dilated cardiomyopathy (NPPA)
familial ovarian cancer (GEN1)
Fanconi anemia complementation group A (FANCA)
hereditary breast carcinoma (GEN1)
hereditary nonpolyposis colon cancer (XRCC4)
hypertrophic cardiomyopathy (CACNB2)
immunodeficiency, common variable, 3 (CD19)
Leigh syndrome (HIBCH)
mitochondrial disease (NDUFS6)
monogenic diabetes (PAX4)
nephronophthisis 4 (NPHP4)
nonsyndromic genetic hearing loss (CDH23, MYO7A)
PHARC syndrome (ABHD12)
platelet-type von Willebrand disease (GP1BA)
PTEN hamartoma tumor syndrome (PTEN)
renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss (ATP6V1B1)
Rothmund-Thomson syndrome (RECQL4)
Schinzel-Giedion syndrome (SETBP1)
short QT syndrome (CACNB2)
syndromic intellectual disability (KMT2C)
turnpenny-fry syndrome (PCGF2)
Usher syndrome type 1 (CDH23, MYO7A)
|
Other WGS-derived genes | AGAP1, AGL, ALDH3A2, AMPD1, ANAPC1, ATP8B3, AURKC, C6, CASP12, CEP170, CHIT1, CHST15, CNOT1, COLQ, CYP21A2, D2HGDH, DSC3, ERCC6L2, FBXO7, FLG2, FUT2, GALNT3, GDPD4, HSD17B13, ITGB2, KCNJ16, LAMA5, LPL, MAPT, MESP1, MROH8, NDUFB9, NOTCH2, NPRL3, OAS1, OR1B1, OR51F1, OR52B4, P2RX5, PDE4DIP, PIGN, POLDIP2, RNF212, SCAPER, SELPLG, SIGLEC12, SLC37A4, SPTBN5, SYNE2, TAP2, TBP, TIGD6, TLR5, TMEM107, TMEM216, TNRC18, TOR1AIP1, TREH, TRPM1, VDR, VRK1, WDR37, ZAN, ZNF141, ZNF83, ZNF844 |