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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)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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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

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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

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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

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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

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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
International/Commercial/For-profit:
$1,789.00USD
U.S. Academic/Non-profit/Government:
$1,110.00USD
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How to Order
  • Ordering Instructions
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  • GM26611 - B-Lymphocyte
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