WIBR3_VPS13C_FS_Homo_H3-1
WIBRe001-A-58
General
Cell Line |
|
| hPSCreg name | WIBRe001-A-58 |
| Cite as: | WIBRe001-A-58 (RRID:CVCL_D3YH) |
| Alternative name(s) |
WIBR3_VPS13C_FS_Homo_H3-1
|
| Cell line type | Human embryonic stem cell (hESC) |
| Similar lines | No similar lines found. |
| Last update | 15th August 2024 |
| Notes | Internal experimental control(s) were generated undergoing the same experimental procedure and are registered as WIBRe001-A-35 and WIBRe001-A-36. |
| User feedback | |
Provider |
|
| Generator | Albert Einstein College of Medicine (AECM) |
| Distributors | |
External Databases |
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| BioSamples | SAMEA115873282 |
| Cellosaurus | CVCL_D3YH |
| Wikidata | Q127384710 |
General Information |
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| Publications | |
| * Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
|
| Subclone of | |
Donor Information
General Donor Information |
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| Sex | female |
| Ethnicity | unknown |
Phenotype and Disease related information (Donor) |
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| Diseases | No disease was diagnosed.
|
| Family history | no |
| Is the medical history available upon request? | no |
| Is clinical information available? | no |
Other Genotyping (Donor) |
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| Is there genome-wide genotyping or functional data available? |
No
|
External Databases (Donor) |
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| BioSamples | SAMEA104129930 |
Ethics
Also have a look at the ethics information for the parental line
WIBRe001-A
.
hESC Derivation
|
The source cell information can be found in the parental cell line
WIBRe001-A.
|
Culture Conditions
| Medium |
Other medium:
Base medium: DMEM/F12
Main protein source: Fetal bovine serum Serum concentration: 15 % |
Characterisation
Analysis of Undifferentiated Cells
| Marker | Expressed | Immunostaining | RT-PCR | Flow Cytometry | Enzymatic Assay | Expression Profiles |
| Alkaline Phosphatase |
Yes |
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| POU5F1 (OCT-4) |
Yes |
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| SSEA-4 |
Yes |
Genotyping
Karyotyping (Cell Line) |
|
| Has the cell line karyotype been analysed? |
Yes
|
Other Genotyping (Cell Line) |
|
Genetic Modification
| Disease/phenotype related modifications |
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