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Brand: ProteoGenix

Human CLDN6 HEK293T Stable Cell Line

Note:
For research use only

$3,550.00

1 vial of 2×10^6 cells + 3550 loyalty points
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Human CLDN6 HEK293T Stable Cell Line

Human CLDN6 HEK293T Stable Cell Line

Product name Human CLDN6 HEK293T Stable Cell Line
Uniprot ID P56747
Expression system Eukaryotic expression
Buffer Freeze Medium: FBS:DMSO=9:1; Culture Medium: DMEM,10S,1%P/S
Delivery condition Dry Ice
Delivery lead time in business days 5-10 business days
Storage condition Liquid Nitrogen
Brand ProteoGenix
Host species HEK293T
Applications FC
Aliases /Synonyms CLDN6 cells
Reference PX-SCL0069
Note For research use only
Target CLDN6
Format Growth Properties: Adherent; Selection Marker: Puromycin (1 μg/mL)
Kit Content 1 vial contains at least 2×10^6 cells in 1 mL Freeze Medium

Introduction

The Human CLDN6 HEK293T Stable Cell Line is a valuable tool for studying the structure, activity, and potential therapeutic applications of the human claudin-6 (CLDN6) protein. This cell line is derived from HEK293T cells, which are a commonly used cell line in biomedical research due to their high transfection efficiency and ability to support the expression of exogenous genes. The stable expression of CLDN6 in this cell line allows for consistent and reliable studies of this important protein.

Structure of CLDN6

CLDN6 is a member of the claudin family of proteins, which are integral membrane proteins involved in the formation of tight junctions between cells. These tight junctions play a critical role in maintaining the barrier function of epithelial and endothelial tissues. CLDN6 is composed of four transmembrane domains, with the N- and C-termini located on the cytoplasmic side of the membrane. It also contains two extracellular loops and a short intracellular loop. This unique structure allows CLDN6 to interact with other proteins and form tight junctions with neighboring cells.

Activity of CLDN6

The main function of CLDN6 is to regulate the permeability of tight junctions. It has been shown to act as a barrier to the diffusion of ions and small molecules, while allowing the selective transport of larger molecules. CLDN6 has also been implicated in the regulation of cell proliferation, differentiation, and migration. Additionally, it has been linked to various signaling pathways involved in cell survival and apoptosis. Dysregulation of CLDN6 has been associated with a number of diseases, including cancer, inflammatory bowel disease, and neurological disorders.

Application as a Therapeutic Target

Given its important role in cellular function and disease, CLDN6 has emerged as a potential therapeutic target. The Human CLDN6 HEK293T Stable Cell Line can be used to study the effects of CLDN6 on various cellular processes and to identify potential drug candidates that can modulate its activity. For example, flow cytometry can be used to analyze the expression of CLDN6 on the surface of cells and to screen for compounds that can disrupt its function. This can lead to the development of novel treatments for diseases associated with CLDN6 dysfunction.
Furthermore, the stable expression of CLDN6 in this cell line allows for the generation of in vitro models for studying diseases that involve CLDN6, such as cancer. These models can be used to investigate the role of CLDN6 in disease progression and to test the efficacy of potential therapies. This can ultimately lead to the development of more targeted and effective treatments for these diseases.

Conclusion

The Human CLDN6 HEK293T Stable Cell Line is a valuable tool for studying the structure, activity, and potential therapeutic applications of CLDN6. Its stable expression of CLDN6 allows for consistent and reliable studies of this important protein, making it an essential resource for researchers in the fields of cell biology, cancer research, and drug discovery. With the ability to study the effects of CLDN6 on various cellular processes and to identify potential drug candidates, this cell line has the potential to contribute to the development of novel treatments for diseases associated with CLDN6 dysfunction.

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