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HighQC™ Human IPSC From Fibroblast-Amyotrophic Lateral Sclerosis

  • For research use only

Cat No.

ABC-SC0212
Product Type

Human iPSCs
Cell Type

Induced Pluripotent Stem Cell
Species

Human
Growth Conditions

37 ℃, 5% CO2
Source Organ

Fibroblast
Disease

Amyotrophic Lateral Sclerosis
Storage

Liquid Nitrogen

HighQC™ Human ALS iPSC from fibroblasts express pluripotency markers,non-tumorigenic, suitable for ALS modeling,neural differentiation,and drug screening.

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  • HighQC™ Human IPSC From Fibroblast-Amyotrophic Lateral Sclerosis
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Home | Stem Cells | Induced Pluripotent Stem Cells (iPSCs) | Induced Pluripotent Stem Cells (iPSCs) | HighQC™ Human IPSC From Fibroblast-Amyotrophic Lateral Sclerosis

Description

HighQC™ Human iPSC from Fibroblast–Amyotrophic Lateral Sclerosis (ALS) is a patient-derived induced pluripotent stem cell (iPSC) line reprogrammed from dermal fibroblasts of individuals with ALS. These cells exhibit typical iPSC morphology with high nucleus-to-cytoplasm ratio, prominent nucleoli, and tight colony formation. Reprogrammed using non-integrating methods, they express core pluripotency markers such as OCT4, SOX2, and NANOG. Karyotype analysis indicates a normal diploid karyotype. They can be differentiated into neural and glial lineages to replicate disease-relevant phenotypes in vitro, making them suitable for investigating disease mechanisms and neurodegeneration.

Product Code

HighQC™ Human IPSC From Fibroblast-Amyotrophic Lateral Sclerosis, Human iPSC-Fibroblast-ALS, hIPSC-F-ALS, Human Fibroblast Derived iPSC ALS
Species

Human
Cat.No

ABC-SC0212
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

Amyotrophic Lateral Sclerosis
Biosafety Level

1
Storage

Liquid Nitrogen
Product Type

Human iPSCs

Application

  • HighQC™ Human iPSC from Fibroblast–Amyotrophic Lateral Sclerosis (ALS) serve as a powerful tool for modeling amyotrophic lateral sclerosis in vitro. They can be differentiated into motor neurons, astrocytes, or oligodendrocytes to study cell-type-specific pathology, gene expression, and neurotoxicity. These cells are also valuable for drug screening, gene-editing validation, and personalized therapeutic development. ALS patient-derived iPSCs enable exploration of disease progression, neuroinflammation, and cellular stress mechanisms within a patient-specific genetic context.

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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