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Tumor Cell Lines

HT-1080

  • For research use only

Cat No.

ABC-TC0424

Product Type

Human Sarcoma Cell Lines

Cell Type

Epithelial

Species

Human

Growth Conditions

37 ℃, 5% CO2

Disease

Fibrosarcoma

Product Code

Ht-1080; HT 1080; HT1080; HT 1080.T

The cells contain an activated N-ras oncogene.

Product Image

Description

HT-1080 is a human fibrosarcoma tumor cell line originally established from a connective tissue biopsy of a 35-year-old Caucasian male with fibrosarcoma, a malignant soft-tissue sarcoma of fibroblastic origin. The cells display an epithelial-like morphology and grow as adherent monolayers in standard culture conditions. Cytogenetic analysis shows a near-diploid karyotype with frequent chromosome abnormalities, and the line harbors an activated N-ras oncogene, a key driver in sarcoma pathobiology. Subsets of HT-1080 cells express markers associated with aggressive tumor behavior and matrix interactions, which have made it a model for studying invasion and metastatic characteristics in vitro. HT-1080 is tumorigenic in immunosuppressed mice, reinforcing its relevance as a malignant tumor model. 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

Ht-1080; HT 1080; HT1080; HT 1080.T

Species

Human

Cat.No

ABC-TC0424

Product Category

Tumor Cell Lines

Size/Quantity

1 vial

Cell Type

Epithelial

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Disease

Fibrosarcoma

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human Sarcoma Cell Lines

Application

  • HT-1080 cell line serves as a versatile in vitro fibrosarcoma model widely used to investigate tumor cell proliferation, invasion, and migration mechanisms and to evaluate anticancer drug responses. Their utility in matrix metalloproteinase (MMP) regulation, extracellular matrix interaction studies, and signal transduction research facilitates exploration of mechanisms driving tumor progression and therapeutic sensitivity in soft-tissue sarcomas.

Citation

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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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