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Transfected Stable Cell Lines

Human NRAS (G13R) BAF3 Cell Line

  • For research use only

Cat No.

ABC-X0014C
Product Type

Overexpression Stable Cell Lines
Cell Type

Lymphocyte
Species

Human
Host Cell

BAF3
Source Organ

Lymphatic
Disease

Normal
Storage

Liquid Nitrogen

The human NRAS (G13R) BAF3 cell line is a powerful tool for studying tumor biology, supporting IL-3 independent proliferation and the mechanisms.

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  • Human NRAS (G13R) BAF3 Cell Line
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Home | Transfected Stable Cell Lines | Overexpression Stable Cell Lines | Human NRAS (G13R) BAF3 Cell Line

Description

Human NRAS (G13R) BAF3 Cell Line is a genetically engineered model derived from selected murine Ba/F3 parental cell line based on customers’ requirement. NRAS (G13R) BAF3 mutant cell line is generated by stable integration of exogenous human NRAS gene harboring the G13R point mutation into Ba/F3 host cells using our optimized transduction of lentiviral vectors.
Target
NRAS encodes a small GTPase involved in transducing signals from receptor tyrosine kinases to downstream pathways including RAF/MEK/ERK and PI3K/AKT. The G13R mutation is a hotspot oncogenic variant that impairs GTP hydrolysis, leading to constitutive NRAS activation. NRAS mutations are frequently associated with hematologic malignancies, melanoma, and colorectal cancer. AcceGen offers generation of stable overexpression and mutation-specific cell lines targeting any gene of your interest. Polyclonal or monoclonal is optional based on customers’ research needs.

Species

Human
Cat.No

ABC-X0014C
Product Category

Transfected Stable Cell Lines
Size/Quantity

1 vial
Cell Type

Lymphocyte
Growth Mode

Suspension
Shipping Info

Dry Ice
Growth Conditions

37 °C, 5% CO₂
Source Organ

Lymphatic
Disease

Normal
Biosafety Level

1
Storage

Liquid Nitrogen
Product Type

Overexpression Stable Cell Lines
Host Cell

BAF3
Quality Control

All cells test negative for mycoplasma, bacteria, yeast, and fungi.

Application

  • The NRAS (G13R) BAF3 Cell Line serves as a powerful tool to investigate RAS-driven transformation and targeted therapeutic approaches. This model enables mechanistic studies of IL-3-independent proliferation, constitutive MAPK activation, and resistance to MEK or RAF inhibitors. It is utilized for high-throughput drug screening and functional validation of anti-RAS strategies.

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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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