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Anti-FPR1 / FPR Antibody (Extracellular Domain) IHC-plus™ LS-A2086


Wt. Vol. Conc. Price
50 µg 50 µl 1 mg/ml Unavailable
Same day shipping In Stock - Same day shipping

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Rabbit Polyclonal to Human FPR1 / FPR
IHC - Paraffin


Human FPR1 / FPR
Human (tested or 100% immunogen sequence identity)
Immunoaffinity purified


IHC - Paraffin (2 µg/ml)

Specificity and Use

FPR1 / FPR antibody was raised against synthetic 16 amino acid peptide from 2nd extracellular domain of human FPR1. Percent identity with other species by BLAST analysis: Human (100%); Chimpanzee, Gorilla (94%); Orangutan (88%); Gibbon (81%).
LS-E28485 - Liquid - 50 µg 1 mg/ml - $145.00
Immunizing peptide used to generate LS-A2086. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
Extracellular Domain
Human FPR1. BLAST analysis of the peptide immunogen showed no homology with other human proteins.


PBS, less than 0.1% sodium azide.
Aliquot and store undiluted at -20°C or below for up to 1 year. Can be stored undiluted at 4°C for up to 1 month. Avoid freeze thaw cycles.
For research use only.

About FPR1 / FPR

P21462 NM_002029 NP_002020.1

FPR1 Antibody, FPR-1 Antibody, FMet-Leu-Phe receptor Antibody, FMLP Antibody, Formyl peptide receptor 1 Antibody, FPR Antibody, N-formyl peptide receptor Antibody, FMLP receptor Antibody, Fpr receptor Antibody, N-formyl peptide receptor 1 Antibody

Formyl peptide receptor 1, a Chemoattractant Receptor, mediates chemotaxis, degranulation, and superoxide production, as part of the inflammatory response. Bacterial N-formylmethionyl peptides and Annexin A1, specific ligands for FPR1, attract polymorphonuclear neutrophils to sites of infection. FPR receptors promote the phosphorylation and downregulation of CCR5, which has been shown to inhibit HIV infection. Therefore, ligands for an FPR receptor may be able to inhibit HIV infection.


Anti-FPR1 antibody LS-A2086 IHC of human tonsil. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.

Requested From: 
Date Requested: 4/28/2017

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