UCSFi001-A-1X

The cell line is not validated yet.

General

Cell Line

hPSCreg name UCSFi001-A-1X
Cite as:
UCSFi001-A-1X
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 23rd March 2026
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Provider

Generator University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
Owner University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
Distributors
Derivation country United States

External Databases

BioSamples SAMEA120998336

General Information

* Is the cell line readily obtainable for third parties?
Yes
Cell line can only be used in: Not-for-profit research only use, obtainable after MTA
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Subclone of

Donor Information

General Donor Information

Sex male
Ethnicity Asian

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Family history N/A
Is the medical history available upon request? No
Is clinical information available? Limited clinical information - EKG

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

Donor Relations

Other cell lines of this donor

External Databases (Donor)

BioSamples SAMEA5843920

Ethics

Also have a look at the ethics information for the parental line UCSFi001-A .
Is there an MTA available for the cell line? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? Addgene
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 UCSFi001-A.
Passage number reprogrammed NA

Reprogramming method

Vector type None

Vector free reprogramming

Other

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 Enzyme-free cell dissociation
EDTA
CO2 Concentration 5 %
Medium mTeSR™ Plus
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
Yes
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
POU5F1 (OCT-4)
Yes
SSEA-4
Yes
Morphology pictures
WTC11 GCamp8f at day 4 after passaging (4X magnification - Bright field).
WTC11 GCamp8f at day 4 after passaging (10X magnification - Bright field).
Differentiation Potency

Microbiology / Virus Screening

Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46, XY
Passage number: 35
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Genetic modifications not related to a disease
Transgene expression
13q32
WTC11c line was engineered by inserting the fast GCaMP8f sensor into the CLYBL safe-harbor locus under the control of the CAG promoter, together with an antibiotic selection cassette removable by Cre recombinase. The clone selected is heterozygous as GCamp8f could buffer intracellular calcium. This line has been successfully differentiated in cardiomyocytes and neurons; calcium transients in both cell types can be monitored in real-time by tracking the green fluorescence.
TALEN
GCamp8f Genotyping final.jpg
Gene editing design and genotyping PCR showing the insertion of the GCamp8f transgene
010-compressed.gif
Calcium transient of Cardiomyocytes derived from WTC11 GCamp8f, tracking GFP fluorescence from the genetically encoded calcium sensor_Video01
011-compressde.gif
Calcium transient of Cardiomyocytes derived from WTC11 GCamp8f, tracking GFP fluorescence from the genetically encoded calcium sensor_Video02