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Stem Cells

HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1

  • For research use only

Cat No.

ABC-SC2048
Product Type

Human iPSCs
Cell Type

Induced Pluripotent Stem Cell
Species

Human
Growth Conditions

37 ℃, 5% CO2
Source Organ

Fibroblast
Disease

Dystrophia Myotonica 1
Storage

Liquid Nitrogen

Cell Type: iPSC; Disease: Dystrophia Myotonica 1; DM1.

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  • HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1
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Home | Stem Cells | Induced Pluripotent Stem Cells (iPSCs) | Induced Pluripotent Stem Cells (iPSCs) | HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1

Description

HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1 is a disease-specific induced pluripotent stem cell line generated from dermal fibroblasts of a donor diagnosed with Myotonic Dystrophy Type 1 (DM1). The resulting iPSCs (induced pluripotent stem cells) exhibit adherent growth and retain the fundamental capacity for trilineage differentiation into ectoderm, mesoderm, and endoderm derivatives. These iPSCs express the core pluripotency marker SSEA-4. They retain DM1-related cellular features and reflect neuromuscular physiology in vivo. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.

Product Code

HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1, HighQC™ hiPSC DM1, hiPSC-DM1, HighQC™ Human Induced Pluripotent Stem Cells From Fibroblast-Myotonic Dystrophy Type 1
Species

Human
Cat.No

ABC-SC2048
Product Category

Stem Cells
Size/Quantity

1 vial
Cell Type

Induced Pluripotent Stem Cell
Growth Mode

Adherent
Shipping Info

Dry Ice
Growth Conditions

37 ℃, 5% CO2
Source Organ

Fibroblast
Disease

Dystrophia Myotonica 1
Storage

Liquid Nitrogen
Product Type

Human iPSCs

Application

  • HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1 serves as a human disease model for developmental and mechanistic studies. Its pluripotent capacity enables differentiation into skeletal muscle cells, cardiomyocytes, and neurons — key lineages affected in myotonic dystrophy type 1 (DM1). This system is used to model multi-systemic pathology, study the toxic effects of expanded Cytosine-Thymine-Guanine (CTG) repeats, and perform drug screening in patient-specific skeletal muscle or cardiac organoids, aiding research into RNA toxicity, muscle development, and cardiac conduction abnormalities.

Citation

When you publish your research, please cite our product as "AcceGen Biotech Cat.# XXX-0000". In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
Customization Options
Tailed to your research

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