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Stem Cells

HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2

  • For research use only

Cat No.

ABC-SC2055

Product Type

Human iPSCs

Cell Type

Induced Pluripotent Stem Cell

Species

Human

Growth Conditions

37 ℃, 5% CO2

Source Organ

Fibroblast

Disease

Tuberous Sclerosis 2

Storage

Liquid Nitrogen

Cell Type: iPSC; Disease: Tuberous Sclerosis 2; TSC2 TSC2 GENE; TSC2.

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Description

HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2 is a disease-specific human induced pluripotent stem cell line derived from dermal fibroblasts of a donor diagnosed with Tuberous Sclerosis Complex (TSC) Type 2, an autosomal dominant disorder caused by mutations in the TSC2 gene. The resulting iPSCs (induced pluripotent stem cells) exhibit adherent growth with a high nucleus-to-cytoplasm ratio. They sustain pluripotency and reflect TSC2-related physiological traits. These cells retain the fundamental capacity for trilineage differentiation into ectoderm, mesoderm, and endoderm derivatives under directed conditions. They express core pluripotency marker SSEA-4. 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-Tuberous Sclerosis 2, HighQC™ hiPSC TSC2, hiPSC-TSC2, HighQC™ Human Induced Pluripotent Stem Cells From Fibroblast-Tuberous Sclerosis Complex 2

Species

Human

Cat.No

ABC-SC2055

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

Tuberous Sclerosis 2

Storage

Liquid Nitrogen

Product Type

Human iPSCs

Gene Info

Gene: TSC2; Mutation: ARG1743GLN

Application

  • HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2 serves as a human in vitro model for developmental and mechanistic studies of tuberous sclerosis. Its pluripotent capacity enables differentiation into disease-relevant lineages, such as neural progenitors and astrocytes, to investigate mTOR pathway dysregulation and cortical tuber formation. This system supports the generation of brain organoids for neurodevelopmental disease modeling and provides a platform for compound screening aimed at identifying potential mTOR inhibitors.

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).

Inquiring HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2

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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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