SHOX2 c.*28T>C_isoWT
MRIi016-A-1
General
Cell Line |
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hPSCreg name | MRIi016-A-1 |
Cite as: | MRIi016-A-1 (RRID:CVCL_D0EA) |
Alternative name(s) |
SHOX2 c.*28T>C_isoWT
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines |
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Last update | 1st February 2023 |
User feedback | |
Provider |
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Generator | Institute of Human Genetics Heidelberg (UKHG) |
Owner | Institute of Human Genetics Heidelberg (UKHG) |
External Databases |
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BioSamples | SAMEA112450469 |
Cellosaurus | CVCL_D0EA |
Wikidata | Q123033122 |
General Information |
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Publications |
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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 | A disease was diagnosed.
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Karyotyping (Donor) |
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Has the donor karyotype been analysed? |
Yes
46 XY
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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 | SAMEA9438087 |
Ethics
Also have a look at the ethics information for the parental line
MRIi016-A
.
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
MRIi016-A.
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Reprogramming method |
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Vector type | Non-integrating |
Vector | Sendai virus |
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
Surface coating | Matrigel/Geltrex |
Feeder cells |
No |
Medium |
Other medium:
Base medium: StemFit
Main protein source: Serum concentration: % |
Characterisation
No characterisation data could be found for this subclone. Please open parental cell line MRIi016-A .Genotyping
Karyotyping (Cell Line) |
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Has the cell line karyotype been analysed? |
Yes
46 XY
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Other Genotyping (Cell Line) |
Genetic Modification
Disease/phenotype related modifications |
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