ARX-CFP/PAX4-mCherry, ARX-T2A-H2B-CFP/H2B-mCherry-RGSHis-T2A-PAX4, ARXnCFP/nCFP/PAX4mCherry/mCherry
HMGUi001-A-46
General
Cell Line |
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hPSCreg name | HMGUi001-A-46 |
Cite as: | HMGUi001-A-46 |
Alternative name(s) |
ARX-CFP/PAX4-mCherry, ARX-T2A-H2B-CFP/H2B-mCherry-RGSHis-T2A-PAX4, ARXnCFP/nCFP/PAX4mCherry/mCherry
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines |
HMGUi001-A (XM001, BIHi043-A) HMGUi001-A-8 (C-PEP-mCherry-hiPSC) HMGUi001-A-43 (hINS-T2A-H2B-Cherry (-/-), hiPSC-INS-T2A-H2B-Cherry reporter, INSCherry/Cherry) HMGUi001-A-5 (ΔINK4 T2D risk region hiPSC) HMGUi001-A-42 (NEUROD2 nVenus/nVenus iPSCs) HMGUi001-A-1 (hINS-T2A-H2B-Cherry (+/-), HMGUi001-A-1) HMGUi001-A-4 (hiPSC-ARX-T2A-H2B-CFP-Flag) HMGUi001-A-22 (NCS1-KO Clone 19) |
Last update | 12th August 2024 |
Notes | This line is a subclone of HMGUi001-A-4. |
User feedback | |
Provider |
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Generator | Institute of Diabetes and Regeneration Research (IDR) |
Owner | Institute of Diabetes and Regeneration Research (IDR) |
Distributors | |
Derivation country | Germany |
External Databases |
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BioSamples | SAMEA115108855 |
General Information |
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Publications | |
* Is the cell line readily obtainable for third parties? |
No |
Subclone of |
Donor Information
General Donor Information |
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Sex | female |
Ethnicity | Caucasian |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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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
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Donor Relations |
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Other cell lines of this donor | |
External Databases (Donor) |
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BioSamples | SAMEA5696688 |
Ethics
Also have a look at the ethics information for the parental line
HMGUi001-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? | Vectors were generated at IDR, pU6-(BbsI)-sgRNA-CAG-Cas9-Venus-bpA plasmid (Addgene plasmid #86986) was used. |
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? | Yes |
Constraints for use or distribution | According to donor consent the line must not be used for commercial purposes. For research purposes project-specific review by a medical Ethics Committee is obligatory. |
hIPSC Derivation
General |
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The source cell information can be found in the parental cell line
HMGUi001-A.
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Passage number reprogrammed | 40 |
Reprogramming method |
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Vector type | Non-integrating |
Vector | The Pax4 locus of HMGUi001 -A-4 hiPSC line was targeted with two vectors. For the first vector, the Cas9- Venus- sgRNA vector, a sgRNA was cloned into the pU6- (BbsI)-sgRNA-CAG- Cas9-Venus- bpA plasmid (Addgene plasmid #86986). Cas9 and a targeting site specific sgRNA were expressed from this vector to induce a double strand break at the targeting region. The second vector contained H2B-mCherry-RGSHis-T2A-PAX4 construct for the intended homology directed repair: the mCherry coding sequence flanked by a 703 bp left homology arm (5’ HA) and a 1009 bp right homology arm (3’ HA). |
Vector free reprogramming |
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Other |
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Selection criteria for clones | Transfected cells expressed Venus and were sorted by FACS. The genotype of the clones was screened by PCR and verified by Sanger sequencing. |
Derived under xeno-free conditions |
Yes |
Derived under GMP? |
No |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Matrigel/Geltrex |
Feeder cells |
No |
Passage method | EDTA |
O2 Concentration | 21 % |
CO2 Concentration | 5 % |
Medium |
Other medium:
Base medium: StemMACS iPS-Brew XF medium
Main protein source: xeno-free Serum concentration: 0 % |
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? | Yes |
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 |
SOX2 |
Yes |
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POU5F1 (OCT-4) |
Yes |
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SSEA-4 |
Yes |
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TRA 1-60 |
Yes |
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Oct-3 |
Yes |
Differentiation Potency
Microbiology / Virus Screening |
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Mycoplasma | Negative |
Genotyping
Karyotyping (Cell Line) |
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Has the cell line karyotype been analysed? |
Yes
46, XX
Karyotyping method:
G-Banding
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Other Genotyping (Cell Line) |
Genetic Modification
Genetic modifications not related to a disease |
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