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HighQC™ Human iPSC-Derived Skeletal Myocyte – Duchenne Muscular Dystrophy Model

  • For research use only

Cat No.

ABC-SC013Y
Product Type

Human Induced Pluripotent Stem Cells
Cell Type

Skeletal Muscle Cells
Species

Human
Growth Conditions

37 ℃, 5% CO2
Source Organ

Skeletal muscle
Disease

Duchenne Muscular Dystrophy
Storage

Liquid Nitrogen

Human iPSC-derived Skeletal Myocyte - Duchenne Muscular Dystrophy Model enables disease modeling, drug screening, and functional muscle biology studies.

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  • HighQC™ Human iPSC-Derived Skeletal Myocyte – Duchenne Muscular Dystrophy Model
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Home | Stem Cells | Induced Pluripotent Stem Cells (iPSCs) | Induced pluripotent stem cell-Derived cells (iPSC-Derived cells) | HighQC™ Human iPSC-Derived Skeletal Myocyte – Duchenne Muscular Dystrophy Model

Description

Skeletal Myocytes DMD Exon 44 Deletion are human Induced Pluripotent Stem Cells-derived skeletal myocytes with a genetically engineered hemizygous deletion in exon 44 of the DMD gene encoding dystrophin. These cells offer a rapidly maturing, consistent, and scalable isogenic system to study Duchenne muscular dystrophy in a human cell model. They are useful for investigating the effects of exon deletion on muscle cell function and for exploring methods to restore dystrophin, such as ASO-mediated exon skipping.

Species

Human
Cat.No

ABC-SC013Y
Quality Control

All cells test negative for mycoplasma, bacteria, yeast, and fungi.
Product Category Stem Cells
Size/Quantity

1 vial
Cell Type

Skeletal Muscle Cells
Growth Mode

Adherent
Shipping Info

Dry Ice
Growth Conditions

37 ℃, 5% CO2
Source Organ

Skeletal muscle
Disease

Duchenne Muscular Dystrophy
Biosafety Level

1
Storage

Liquid Nitrogen
Product Type

Human Induced Pluripotent Stem Cells

Application

  • For research use only

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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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