Short Decsription
Creative Biolabs offers HEK293T-Tg(Human FPR2 Receptor) Division-Arrested Cell which FPR2 receptor stably expressed in HEK293T cells.
Description
HEK293T-Tg(Human FPR2 Receptor) Division-Arrested Cell was engineered to express the receptor human FPR2 (NM_001462.3). This cell line can be used to study FPR2 receptor function, signaling pathways, and potential therapeutic interventions. Dividing-arrest cells are cells that are normally kept under specific culture conditions or treated with agents that prevent cell division from being held in a non-dividing state. This can be achieved through methods such as serum starvation, chemical inhibitors of cell cycle progression, or genetic modification.
Features
Well-characterized stable cell lines;
for cell-based high-throughput screening;
Low-cost evaluation of stable cell lines or limited quantities of compounds.
Applications
FPR2 receptor function, signaling pathways, and potential therapeutic interventions.
Protein Target
GPCR
Receptor Name
FPR2
Receptor Family
N-formylpeptide
Species
Human
Parental Cell Line
HEK293T
Transfection
Expression vector containing full-length human FPR2 cDNA (GenBank Accession Number NM_001462.3) with FLAG tag sequence at N-terminus
Gene
NM_001462.3
Background
The lipoxin A4 receptor ALX is also known as formyl peptide receptor- like 1 (FPRL1) or formyl peptide receptor 2 (FPR2). It shares 69% amino acid identity with FPR but displays low affinity for bacterial peptide N-formyl-methionyl- leucyl-phenylalanine (fMLF). ALX is highly expressed on neutrophils and monocytes and mediates cell chemotaxis. By interacting with a variety of exogenous and host- derived agonists, ALX may have important implications in the pathogenesis of human diseases such as HIV, Alzheimer's disease (AD), amyloidosis and prion diseases.

For Research Use Only | Not For Clinical Use

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