Stem Cells

HighQC™ Human Induced Pluripotent Stem Cells, From Amyotrophic Lateral Sclerosis

  • For research use only

Cat No.

ABC-SC0211

Product Type

Human iPSCs

Cell Type

Induced Pluripotent Stem Cell

Species

Human

Growth Conditions

37 ℃, 5% CO2

Disease

Amyotrophic Lateral Sclerosis

Storage

Liquid Nitrogen

Amyotrophic Lateral Sclerosis, female donor, Primary cell type: Fibroblast

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Description

HighQC™ human induced pluripotent stem cells derived from skin fibroblasts of patients with amyotrophic lateral sclerosis (ALS). These cells exhibit a high nuclear-to-cytoplasmic ratio with prominent nucleoli and grow as compact colonies under feeder-free, adherent conditions. These cells are generated by transducing OCT4, SOX2, KLF4, and c-MYC into patient-derived skin fibroblasts using Sendai virus. They express pluripotency markers including OCT4, SSEA4. These cells exhibit self-renewal capacity and retain the full pluripotent differentiation potential into all three germ layers—ectoderm, mesoderm, and endoderm under directed differentiation protocols. Each lot undergoes rigorous screening and isolation procedures, and is rigorously tested to ensure it is free of contamination from HIV-1, HBV, HCV, syphilis, mycoplasma, fungi, yeast, and bacteria.

Product Code

HighQC™ Human Induced Pluripotent Stem Cells, From Amyotrophic Lateral Sclerosis, Human iPSC-ALS, hIPSC-ALS, Human Induced Pluripotent Stem Cells ALS

Species

Human

Cat.No

ABC-SC0211

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

Disease

Amyotrophic Lateral Sclerosis

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human iPSCs

Application

  • HighQC™ Human Induced Pluripotent Stem Cells, From Amyotrophic Lateral Sclerosis serve as a powerful tool for advancing research into neurodegenerative diseases. These patient-specific cells can be differentiated into motor neurons, astrocytes, and other central nervous system cell types, enabling detailed modeling of Amyotrophic Lateral Sclerosis (ALS) pathology in vitro. These cells represent an ALS patient-derived iPSC line, supporting disease-specific modeling and mechanistic studies of amyotrophic lateral sclerosis.

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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