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Brand: ProteoGenix

Human FOLH1/PSMA 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 FOLH1/PSMA HEK293T Stable Cell Line

Human FOLH1/PSMA HEK293T Stable Cell Line

Product name Human FOLH1/PSMA HEK293T Stable Cell Line
Uniprot ID Q04609
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 FOLH1/PSMA cells
Reference PX-SCL0026
Note For research use only
Target FOLH1/PSMA
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 FOLH1/PSMA HEK293T Stable Cell Line is a valuable tool for studying the structure, activity, and application of the human folate hydrolase 1/prostate-specific membrane antigen (FOLH1/PSMA) protein. This stable cell line is derived from the human embryonic kidney (HEK) 293T cell line and is engineered to stably express the FOLH1/PSMA protein. In this article, we will delve into the details of this stable cell line and its use in flow cytometry and as a therapeutic target.

Structure of FOLH1/PSMA

FOLH1/PSMA is a type II transmembrane protein that is highly expressed in prostate cancer cells. It is composed of 750 amino acids and has a molecular weight of approximately 100 kDa. The protein contains a cytoplasmic domain, a transmembrane domain, and an extracellular domain. The extracellular domain of FOLH1/PSMA contains the enzymatic activity responsible for the hydrolysis of folate and the cleavage of the prostate-specific antigen (PSA). This unique structure makes FOLH1/PSMA a potential target for both diagnostic and therapeutic purposes.

Activity of FOLH1/PSMA

The enzymatic activity of FOLH1/PSMA plays a crucial role in the progression of prostate cancer. It is involved in the uptake of folate, which is essential for the growth and proliferation of cancer cells. Additionally, FOLH1/PSMA is responsible for the cleavage of PSA, a biomarker for prostate cancer. This cleavage leads to the release of PSA into the bloodstream, making it a useful diagnostic tool for prostate cancer. The overexpression of FOLH1/PSMA in prostate cancer cells makes it an attractive target for therapeutic interventions.

Application in Flow Cytometry

The Human FOLH1/PSMA HEK293T Stable Cell Line is a valuable tool for studying the expression and activity of FOLH1/PSMA in prostate cancer cells. This stable cell line can be used in flow cytometry experiments to detect the expression of FOLH1/PSMA on the cell surface. The cells can be stained with a specific antibody against FOLH1/PSMA and analyzed using a flow cytometer. This allows for the quantification of FOLH1/PSMA expression in different cell populations and can provide valuable insights into the role of this protein in prostate cancer.

Therapeutic Target

The overexpression of FOLH1/PSMA in prostate cancer cells makes it an attractive therapeutic target. Several studies have shown that targeting FOLH1/PSMA can lead to the inhibition of cancer cell growth and the induction of apoptosis. The Human FOLH1/PSMA HEK293T Stable Cell Line can be used to screen potential drugs or compounds that can specifically target FOLH1/PSMA. This stable cell line can also be used to study the mechanism of action of these compounds and their potential for clinical use.

Conclusion

In summary, the Human FOLH1/PSMA HEK293T Stable Cell Line is a valuable tool for studying the structure, activity, and application of FOLH1/PSMA in prostate cancer. Its use in flow cytometry allows for the detection and quantification of FOLH1/PSMA expression, while its potential as a therapeutic target makes it a promising tool for drug discovery and development. Further research using this stable cell line can provide valuable insights into the role of FOLH1/PSMA in prostate cancer and potentially lead to the development of new and effective treatments for this disease.

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