WTSIi020-A
HPSI0114i-eipl_1
iPSC line
At European Collection of Authenticated Cell Cultures (ECACC)
A CLIP contains information about a cell line including any
specific third party obligations relating to, for example,
licensing obligations or the donor consent which affect the
use of the cell line.
A batch specific Certificate of Analysis will be available to
download once you receive your EBiSC iPSC line.
General#
Cell Line |
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hPSCreg Name | WTSIi020-A |
Alternative name(s) |
HPSI0114i-eipl_1
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Provider |
|
Depositor | Wellcome Sanger Institute (WTSI) |
Distributors |
EBiSC
European Collection of Authenticated Cell Cultures (ECACC)
|
Derivation country | United Kingdom |
External Databases |
|
hPSCreg | WTSIi020-A |
BioSamples | SAMEA2536417 |
HipSci | HPSI0114i-eipl_1 |
Cellosaurus | CVCL_AE06 |
ECACC | 77650081, 66540090 |
CLO | CLO_0100978 |
Wikidata | Q54890417 |
General Information |
|
Publications | View all related publications on hPSCreg (3) |
* Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
|
Donor Information#
General Donor Information |
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Sex | female |
Age of donor (at collection) | 40-44 |
Ethnicity | White - White British |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Donor Relations |
|
Other cell lines of this donor | |
External Databases (Donor) |
|
BioSamples | SAMEA2398480 |
HipSci | HPSI-eipl |
hIPSC Derivation#
General |
|
Source cell type |
fibroblastA 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.
|
Source cell origin |
zone of skinAny portion of the organ that covers that body and consists of a layer of epidermis and a layer of dermis.
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Age of donor (at collection) | 40-44 |
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#
Latest released batch |
|
Culture medium | Essential E8 |
Passage method | EDTA |
Surface coating | Vitronectin |
O2 concentration | 21 |
CO2 concentration | 5 |
Temperature | 37 |
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 | FACS | Enzymatic Assay | Expression Profiles |
POU5F1 (OCT-4) |
Yes |
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SOX2 |
Yes |
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NANOG |
Yes |
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SSEA-1 |
No |
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SSEA-4 |
Yes |
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TRA 1-60 |
Yes |
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Pluripotency Score | Novelty Score | Link to microarray data |
17.743 | 1.158 | http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4057/ |
Report
HPSI-eipl.pluritest.pluripotency_score.20161010.png
pluripotency image
HPSI-eipl.pluritest.novelty_score.20161010.png
novelty image
Microbiology / Virus Screening |
|
HIV 1 | Negative |
HIV 2 | Negative |
Hepatitis B | Negative |
Hepatitis C | Negative |
Mycoplasma | Negative |
Sterility |
|
Inoculation for microbiological growth | No Contaminants Detected |
Mycoplasma | Not Detected |
Viability | Viable post-cryopreservation |
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/ERZ123002
cnv
http://www.hipsci.org/lines/#/lines/HPSI0114i-eipl_1 Number of regions different from primary tissue: 0; Length of differences from primary tissue: 0
Methylation profiling
http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4059/ Text file with probe intensities |
WGS-derived disease associations |
Charcot-Marie-Tooth disease (FIG4, HINT1)
Cohen syndrome (VPS13B)
complex neurodevelopmental disorder (CNTNAP2, SETBP1)
demyelinating hereditary motor and sensory neuropathy (MTMR2)
dilated cardiomyopathy (NPPA)
Fanconi anemia complementation group A (FANCA)
Hermansky-Pudlak syndrome 4 (HPS4)
intellectual disability (CDH15)
microcephaly, seizures, and developmental delay (PNKP)
mitochondrial disease (NDUFS6)
monogenic diabetes (PAX4)
mucopolysaccharidosis type 4A (GALNS)
myopathy caused by variation in POMT1 (POMT1)
nephronophthisis 4 (NPHP4)
nonsyndromic genetic hearing loss (CDH23, TMPRSS3)
Noonan syndrome (MRAS)
primary ciliary dyskinesia 7 (DNAH11)
renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss (ATP6V1B1)
Rothmund-Thomson syndrome (RECQL4)
Schinzel-Giedion syndrome (SETBP1)
Smith-Magenis syndrome (RAI1)
syndromic intellectual disability (KMT2C)
turnpenny-fry syndrome (PCGF2)
Usher syndrome type 1 (CDH23)
X-linked complex neurodevelopmental disorder (ZNF711)
|
Other WGS-derived genes | AGAP6, ALDH3A2, ANAPC1, ARMS2, AURKC, BMP4, CARD8, CASP12, CATSPER2, CHST15, COG2, COLQ, CST3, CYP21A2, CYP2D6, CYP2F1, D2HGDH, DEFB126, DSC3, ERCC6L2, FLG2, FUT2, FZD6, GALNT3, GDPD4, GLYCTK, GPRIN1, IL12RB1, IRF5, ITGB2, KCNJ16, MAPT, MICA, MROH8, NDUFB9, NFU1, NLRC4, NOTCH2, NPRL3, OPRM1, OR1B1, OR51F1, OR52B4, OTOR, P2RX5, PDE4DIP, PIGN, PITX2, POLDIP2, PRKRA, PTCHD3, PYGL, RP9, RXFP2, SELPLG, SLC37A4, SRA1, STAG2, TGIF1, TIGD6, TMEM107, TMEM216, TMPRSS6, TNRC18, TPTE, TREH, TRPM1, WDR37, ZAN |