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Transfected Stable Cell Lines

Human BRAF (G469A) NIH/3T3 Cell Line

  • For research use only

Cat No.

ABC-X0046C
Product Type

Overexpression Stable Cell Lines
Cell Type

Fibroblast
Species

Human
Host Cell

NIH/3T3
Source Organ

Embryo
Disease

Normal
Storage

Liquid Nitrogen

The human BRAF (G469A) NIH/3T3 cell line provides a reliable platform for tumor research, supporting high-throughput screening and BRAF-dependent studies.

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  • Human BRAF (G469A) NIH/3T3 Cell Line
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Home | Transfected Stable Cell Lines | Overexpression Stable Cell Lines | Human BRAF (G469A) NIH/3T3 Cell Line

Description

Human BRAF (G469A) NIH/3T3 Cell Line is a genetically engineered model derived from murine NIH/3T3 fibroblasts based on customers’ requirement. BRAF (G469A) NIH/3T3 mutant cell line is created by stable integration of the human BRAF gene carrying the G469A mutation into NIH/3T3 cells using our proprietary lentiviral transduction approach.
Target
BRAF is a serine/threonine-protein kinase in the RAS-RAF-MEK-ERK signaling cascade. The G469A mutation, located in the activation segment of the kinase domain, enhances kinase activity and promotes tumorigenesis independent of upstream signals. It has been implicated in lung and colorectal cancers. AcceGen provides precise oncogenic models for pathway elucidation and drug testing. Polyclonal or monoclonal is optional based on customers’ research needs.

Species

Human
Cat.No

ABC-X0046C
Product Category

Transfected Stable Cell Lines
Size/Quantity

1 vial
Cell Type

Fibroblast
Growth Mode

Adherent
Shipping Info

Dry Ice
Growth Conditions

37 °C, 5% CO₂
Source Organ

Embryo
Disease

Normal
Biosafety Level

1
Storage

Liquid Nitrogen
Product Type

Overexpression Stable Cell Lines
Host Cell

NIH/3T3
Quality Control

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

Application

  • The BRAF (G469A) NIH/3T3 Cell Line serves as a reliable platform to assess BRAF-dependent transformation, MAPK pathway activation, and resistance to BRAF or MEK inhibitors. It is useful for preclinical studies and high-throughput screening of pathway-targeted therapies.

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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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