WTSIi181-A
HPSI0514i-rutc_2
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 |
|
| hPSCreg Name | WTSIi181-A |
| Alternative name(s) |
HPSI0514i-rutc_2
|
| Cell line type | Human induced pluripotent stem cell (hiPSC) |
| Similar lines | |
Provider |
|
| Depositor | Wellcome Sanger Institute (WTSI) |
| Distributors |
EBiSC
European Collection of Authenticated Cell Cultures (ECACC)
|
| Derivation country | United Kingdom |
External Databases |
|
| hPSCreg | WTSIi181-A |
| BioSamples | SAMEA3974014 |
| HipSci | HPSI0514i-rutc_2 |
| Cellosaurus | CVCL_AX03 |
| ECACC | 77650311, 66540354 |
| CLO | CLO_0101182 |
| Wikidata | Q54890922 |
General Information |
|
| Publications | View all related publications on hPSCreg (1) |
| * 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 |
|
| Sex | female |
| Age of donor (at collection) | 60-64 |
| Ethnicity | White - White British |
Phenotype and Disease related information (Donor) |
|
| Diseases | No disease was diagnosed.
|
External Databases (Donor) |
|
| BioSamples | SAMEA2533335 |
| HipSci | HPSI-rutc |
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.
|
| 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 | FACS | Enzymatic Assay | Expression Profiles |
| POU5F1 (OCT-4) |
Yes |
|
||||
| SOX2 |
Yes |
|
||||
| NANOG |
Yes |
|
| Pluripotency Score | Novelty Score | |
| 21.134 | 1.27 |
Report
HPSI-rutc.pluritest.pluripotency_score.20161010.png
pluripotency image
HPSI-rutc.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
cnv
http://www.hipsci.org/lines/#/lines/HPSI0514i-rutc_2 Number of regions different from primary tissue: 1; Length of differences from primary tissue: 1
Methylation profiling
http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-4059/ Text file with probe intensities |
| WGS-derived disease associations |
arrhythmogenic right ventricular cardiomyopathy (TTN)
Charcot-Marie-Tooth disease (FIG4)
Cohen syndrome (VPS13B)
complex neurodevelopmental disorder (CNTNAP2, SETBP1)
demyelinating hereditary motor and sensory neuropathy (MTMR2)
dilated cardiomyopathy (NPPA, TTN)
hypertrophic cardiomyopathy (TTN)
mitochondrial disease (NDUFS6)
monogenic diabetes (PAX4)
myopathy, myofibrillar, 9, with early respiratory failure (TTN)
nephronophthisis 4 (NPHP4)
nonsyndromic genetic hearing loss (CDH23, LOXHD1)
PHARC syndrome (ABHD12)
platelet-type bleeding disorder 11 (GP6)
primary ciliary dyskinesia 7 (DNAH11)
Rothmund-Thomson syndrome (RECQL4)
Schinzel-Giedion syndrome (SETBP1)
Smith-Magenis syndrome (RAI1)
syndromic intellectual disability (KMT2C)
tibial muscular dystrophy (TTN)
TTN-related myopathy (TTN)
Usher syndrome type 1 (CDH23)
|
| Other WGS-derived genes | AGAP1, AGAP6, AGL, ATP13A5, AURKC, BMP4, CARD8, CASP12, CATSPER2, CHIT1, CHST15, CST3, CYP2D6, CYP2F1, CYP3A5, CYP4B1, D2HGDH, DEFB126, DSC3, DUSP6, FCGR2A, FUT2, GALNT3, GLYCTK, HLA-DRB5, HSD17B13, IDO2, IL12RB1, INMT, IRF5, ITGB2, KCNJ16, LAMA5, LPL, MAPT, MESP1, MROH8, MYH15, NBAS, NDUFB9, NFU1, NPRL3, OAS1, OR1B1, P2RX5, PADI2, PDE4DIP, PIGN, PITX2, POLDIP2, PRKRA, RNF212, SCAPER, SLC37A4, SYNE2, TDG, TGIF1, TIGD6, TMEM107, TMEM216, TMPRSS6, TNRC18, TREH, TRPM1, VDR, WDR37, ZNF141, ZNF527, ZNF83 |