Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal FPRL1/RFP antibody. Carrier free. Suitable for IHC-P, ICC/IF and reacts with Transfected cell line, Human samples.
View Alternative Names
FPRH1, FPRL1, LXA4R, FPR2, N-formyl peptide receptor 2, FMLP-related receptor I, Formyl peptide receptor-like 1, HM63, Lipoxin A4 receptor, RFP, FMLP-R-I, LXA4 receptor
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling FPRL1/RFP + FPR3 with ab317815 at 1/500 (0.982 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : no staining on human cerebrum. The section was incubated with ab317815 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a FPR2 expression vector containing a Myc-His tag. (B) HEK-293T transfected with FPR3 expression vector containing a Myc-His tag. (C) HEK-293T transfected with a FPR1 expression vector containing a Myc-His tag. (D) HEK-293T transfected with empty vector containing a Myc-His tag. tissue labeling FPRL1/RFP + FPR3 with ab317815 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
This antibody recognizes both FPR2 and FPR3. Positive staining on (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a FPR2 expression vector containing a Myc-His tag and (B) HEK-293T transfected with a FPR3 expression vector containing a Myc-His tag, negative staining on (C) HEK-293T transfected with a FPR1 expression vector containing a Myc-His tag and (D) HEK-293T transfected with empty vector containing a Myc-His tag. The section was incubated with ab317815 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human lung tissue labeling FPRL1/RFP + FPR3 with ab317815 at 1/500 (0.982 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on neutrophils of human lung. The section was incubated with ab317815 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human spleen tissue labeling FPRL1/RFP + FPR3 with ab317815 at 1/500 (0.982 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on neutrophils of human spleen (PMID : 9151906). The section was incubated with ab317815 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cardiac muscle tissue labeling FPRL1/RFP + FPR3 with ab317815 at 1/500 (0.982 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on neutrophils of human cardiac muscle. The section was incubated with ab317815 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94] - BSA and Azide free (AB317816)
This data was developed using ab317815, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Human PBMC (human peripheral blood mononuclear cell) cells labelling FPRL1/RFP + FPR3 with ab317815 at 1/100 (4.91 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing cytoplasmic staining in CD14 positive cells of human PBMC (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-human CD14 mouse monoclonal antibody (Alexa Fluor® 647) was used to counterstain tubulin at 1/200 2.5 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
Related conjugates and formulations (1)
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Anti-FPRL1/RFP + FPR3 antibody [EPR28515-94]
Reactivity data
Product details
ab317816 is the carrirer-free version of ab317815.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
FPRL1 engages in modulating inflammation and host defense against pathogens. It belongs to the GPCR family which plays a central role in cellular signaling networks. FPRL1 does not function alone but instead often associates with other proteins and receptors to navigate diverse immune responses. Its engagement with formyl peptides leads to activation of immune cells promoting chemotaxis degranulation and production of reactive oxygen species. This receptor is also involved in sensing danger signals participating in the clearance of apoptotic cells.
Pathways
FPRL1 influences the MAPK and NF-kB signaling pathways both important for immune response regulation and inflammation. The receptor's pathway interactions contribute to cellular responses like cytokine production and apoptosis regulation. FPRL1 interacts with related proteins such as FPR1 which share overlapping ligand specificity and functional roles. Through these pathways FPRL1 can modulate immune responses that protect the host from infection or contribute to inflammatory diseases.
Product protocols
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Target data
Additional targets
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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