Human Formyl Peptide Receptor 2 (FPR2) Protein

Este producto es parte de FPR - Formyl Peptide Receptor
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2210€ (1 mg)

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935106861
info@markelab.com
name
Human Formyl Peptide Receptor 2 (FPR2) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx653459
tested applications
WB, SDS-PAGE

Description

Human Formyl Peptide Receptor 2 (FPR2) Protein is a Recombinant Human protein expressed in E. coli.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryProteins and Peptides
Immunogen TargetFormyl Peptide Receptor 2 (FPR2)
HostE. coli
OriginHuman
ConjugationUnconjugated
Observed MWConcentration: Prior to lyophilization: 200 µg/ml Sequence Fragment: Please enquire. Tag: N-terminal His tag
ExpressionRecombinant
Purity> 90%
Size 11 mg
Size 25 mg
FormLyophilized To keep the original salt concentration, we recommend reconstituting to the original concentration prior to lyophilization (see Concentration) in ddH2O. If a lower concentration is required, dilute in PBS, pH 7.4. If a higher concentration is required, the product can be reconstituted directly in PBS, pH 7.4, though please note that this will change the overall salt concentration. The stock concentration should be between 0.1-1.0 mg/ml. Do not vortex.
Tested ApplicationsWB, SDS-PAGE
BufferPrior to lyophilization: PBS, pH 7.4, containing 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose and Proclin-300.
AvailabilityShipped within 1-2 months.
StorageStore at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles.
Dry IceNo
AliasFPR2,ALXR,FMLPX,FPRH1,LXA4R,ALX,FPRH2,FPRL1,RFP,formyl peptide receptor-like 1,HM63,FMLP-R-II
BackgroundProtein FPR2
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

FPR2, also known as ALX/FPR2, is a G protein-coupled receptor with dual roles in pro- and anti-inflammatory signaling. It is expressed on neutrophils, macrophages, and epithelial cells, where it recognizes formylated peptides, lipoxin A4, and other endogenous or pathogen-derived ligands. FPR2 signaling activates pathways like PI3K/Akt and MAPK, regulating immune cell chemotaxis, phagocytosis, and cytokine production. Uniquely, FPR2 mediates both inflammatory responses and resolution of inflammation, depending on the ligand. For example, it promotes inflammation in response to bacterial peptides but facilitates resolution through lipoxin A4, which reduces neutrophil recruitment and promotes tissue repair. Dysregulation of FPR2 is linked to chronic inflammation, autoimmune diseases, and sepsis. In cancer, FPR2 can either support or inhibit tumor progression by influencing immune cell behavior and tumor microenvironment composition. FPR2’s ability to switch between pro- and anti-inflammatory states highlights its therapeutic potential for modulating inflammation, resolving chronic inflammatory diseases, and targeting immune dysfunction in cancer.

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