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GM28561
iPSC
from
Fibroblast
Description:
ISOGENIC CONTROL
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG
N-GLYCANASE 1; NGLY1
Affected:
Yes
Sex:
Female
Age:
16
YR
(At Sampling)
Sample Description
Overview
Characterizations
Phenotypic Data
External Links
Culture Protocols
Overview
Repository
NIGMS Human Genetic Cell Repository
Subcollection
Gene-Edited hiPSC
Heritable Diseases
PIGI Consented Sample
Protocols
Protocol PDF
Biopsy Source
Skin
Cell Type
Stem cell
Cell Subtype
Induced pluripotent stem cell
Transformant
Reprogrammed (Sendai)
Sample Source
iPSC from Fibroblast
Race
White
Ethnicity
Not Hispanic/Latino
Ethnicity
British/English
Country of Origin
USA
Family Member
1
Family History
N
Relation to Proband
proband
Confirmation
Molecular characterization before cell line submission to CCR
ISCN
46,XX[18]
Species
Homo
sapiens
Common Name
Human
Remarks
Gene corrected isogenic iPSC line (NCATS-CL6105/TRNDi010-D-2) generated from parental fibro GM26612 carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9; homozygous correction - PMID 34619643. Researchers purchasing hiPSCs from the NIGMS Repository are responsible for any limited use label licenses (LULLs) applicable to the cell line purchased. The applicable LULL to this line is
Sendai-CytoTune
. This line was gene-edited using CRISPR/Cas9 technology using a
LULL agreement with The Broad Institute
. Please see Phenotypic Data tab of parental fibro GM26612 for additional line information.
Characterizations
Passage Frozen
31
Induced Pluripotent Stem Cell
The frozen cell line submitted to the Repository was recovered and expanded. The expanded line was evaluated for viability surface antigen expression and alkaline phosphatase activity. Pluripotency was assessed via embryoid body (EB) formation. Steady-state mRNA expression patterns of undifferentiated iPSC and EBs were determined via real-time PCR. Characterization data are included in the
Certificate of Analysis.
Phenotypic Data
Remarks
Gene corrected isogenic iPSC line (NCATS-CL6105/TRNDi010-D-2) generated from parental fibro GM26612 carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9; homozygous correction - PMID 34619643. Researchers purchasing hiPSCs from the NIGMS Repository are responsible for any limited use label licenses (LULLs) applicable to the cell line purchased. The applicable LULL to this line is
Sendai-CytoTune
. This line was gene-edited using CRISPR/Cas9 technology using a
LULL agreement with The Broad Institute
. Please see Phenotypic Data tab of parental fibro GM26612 for additional line information.
External Links
Gene Cards
NGLY1
NCBI GTR
610661 N-GLYCANASE 1; NGLY1
615273 CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG
OMIM
610661 N-GLYCANASE 1; NGLY1
615273 CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG
Culture Protocols
Passage Frozen
31
Split Ratio
1:8
Temperature
37 C
Percent CO2
5%
Percent O2
AMBIENT
Medium
mTeSR1
Serum
0% none
Substrate
Matrigel
Supplement
-
Pricing
Commercial/For-profit:
$1,789.00
USD
Academic/Non-profit/Government:
$1,110.00
USD
Add to Cart
How to Order
Ordering Instructions
MTA / Assurance Form
Statement of Research Intent Form
Related Products
Same Subject
GM26611 - B-Lymphocyte
GM26612 - Fibroblast
Same Family
3377
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