iPSC-REEP1_hetKO2
The cell line is not validated yet.
HIHCNi008-A-4
General
Cell Line |
|
| hPSCreg name | HIHCNi008-A-4 |
| Cite as: | HIHCNi008-A-4 (RRID:CVCL_D5HA) |
| Alternative name(s) |
iPSC-REEP1_hetKO2
|
| Cell line type | Human induced pluripotent stem cell (hiPSC) |
| Similar lines |
HIHCNi008-A (iPSC-CO-4) HIHCNi008-A-3 (iPSC-REEP1_homKO2) |
| Last update | 20th November 2024 |
| User feedback | |
Provider |
|
| Generator | Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN) |
External Databases |
|
| BioSamples | SAMEA115125887 |
| Cellosaurus | CVCL_D5HA |
| Wikidata | Q127381755 |
General Information |
|
| Publications | |
| * Is the cell line readily obtainable for third parties? |
No |
| Subclone of | |
Donor Information
General Donor Information |
|
| Sex | male |
| Ethnicity | caucasian |
Phenotype and Disease related information (Donor) |
|
| Diseases | No disease was diagnosed.
|
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 | SAMEA115124423 |
Ethics
Also have a look at the ethics information for the parental line
HIHCNi008-A
.
| For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? |
hIPSC Derivation
General |
|
|
The source cell information can be found in the parental cell line
HIHCNi008-A.
|
|
Reprogramming method |
|
| Vector type | Non-integrating |
| Vector | Episomal |
| Is reprogramming vector detectable? |
No |
| Methods used |
PCR
|
Vector free reprogramming |
|
Other |
|
| Derived under xeno-free conditions |
Unknown |
| Derived under GMP? |
Unknown |
| Available as clinical grade? |
Unknown |
Culture Conditions
| Medium |
Essential 8™
|
Characterisation
Analysis of Undifferentiated Cells
Differentiation Potency
In vitro spontaneous differentiation
Morphology
Genotyping
Karyotyping (Cell Line) |
|
Other Genotyping (Cell Line) |
Genetic Modification
| Disease/phenotype related modifications |
|
Login to share your feedback, experiences or results with the research community.