SCAUi001-A-2
General
Cell Line |
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hPSCreg name | SCAUi001-A-2 |
Cite as: | SCAUi001-A-2 (RRID:CVCL_D0KZ) |
Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines |
LUMCi056-A-1 (LUMC0128iCRB01 heterozygote CRISPR corrected isogenic clone 02, iso02LUMC0128iCRB01) Donor's gene variants: CRB1, CRB1 Donor diseases: Retinitis Pigmentosa WAe001-A-10 (H1_RB1ex3_G3) RUCDRi002-A-63 (LVIP05-RB1-CS1) WAe001-A-11 (H1_RB1ex3_G4) RUCDRi002-A-64 (LVIP05-RB1-CS2) WAe001-A-31 (H1_RB1ex1_D6) RUCDRi002-A-65 (LVIP05-RB1-CS3) WAe001-A-32 (H1_RB1ex1_E9) |
Last update | 20th September 2023 |
User feedback | |
Provider |
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Generator | South China Agricultural University (SCAU) |
External Databases |
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BioSamples | SAMEA114402034 |
Cellosaurus | CVCL_D0KZ |
Wikidata | Q123033405 |
General Information |
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* Is the cell line readily obtainable for third parties? |
Yes Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
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Subclone of |
Donor Information
General Donor Information |
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Sex | male |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Family history | N/A |
Is the medical history available upon request? | N/A |
Is clinical information available? | N/A |
Other Genotyping (Donor) |
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Is there genome-wide genotyping or functional data available? |
No
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External Databases (Donor) |
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BioSamples | SAMEA114396408 |
Ethics
Also have a look at the ethics information for the parental line
SCAUi001-A
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For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? |
hIPSC Derivation
General |
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The source cell information can be found in the parental cell line
SCAUi001-A.
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Reprogramming method |
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Vector type | None |
Vector free reprogramming |
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Other |
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Derived under xeno-free conditions |
Unknown |
Derived under GMP? |
Unknown |
Available as clinical grade? |
Unknown |
Culture Conditions
Medium |
Essential 8™
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Characterisation
No characterisation data could be found for this subclone. Please open parental cell line SCAUi001-A .Genotyping
Karyotyping (Cell Line) |
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Other Genotyping (Cell Line) |
Genetic Modification
Disease/phenotype related modifications |
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