Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal CX3CR1 antibody. Carrier free. Suitable for WB, IHC-P, IP and reacts with Mouse, Rat samples.
View Alternative Names
CMKBRL1, GPR13, CX3CR1, CX3C chemokine receptor 1, C-X3-C CKR-1, Beta chemokine receptor-like 1, Fractalkine receptor, G-protein coupled receptor 13, V28, CMK-BRL-1, CMK-BRL1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscl tissue labelling CX3CR1 with ab308613 at 1/1000 (0.479 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on mouse skeletal muscle. The section was incubated with ab308613 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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 Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labelling CX3CR1 with ab308613 at 1/1000 (0.479 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on immune cells of mouse lung. The section was incubated with ab308613 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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 Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling CX3CR1 with ab308613 at 1/1000 (0.479 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on microglial cells of mouse cerebrum. The section was incubated with ab308613 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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 Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
Immunohistochemical analysis of paraffin-embedded Mouse breast cancer tissue labelling CX3CR1 with ab308613 at 1/1000 (0.479 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on immune cells of mouse breast cancer. The section was incubated with ab308613 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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 Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
This data was developed using ab308613, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) Cerebrum tissue from wild-type C57BL/6J mice and (B) Cerebrum tissue from Cx3cr1 knockout mice tissue labeling CX3CR1 with ab308613 at 1/2000 dilution.
Positive staining on (A) Cerebrum tissue from wild-type C57BL/6J mice, and no staining on (B) Cerebrum tissue from Cx3cr1 knockout mice.
The primary antibody was incubated for 30 mins at room temperature. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.
The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Cx3cr1-KO homozygous mice (Strain ID : T006121).
- IP
Supplier Data
Immunoprecipitation - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
This data was developed using ab308613, the same antibody clone in a different buffer formulation.CX3CR1 was immunoprecipitated from 0.35 mg Mouse spinal cord tissue lysate with ab308613 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab308613 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Mouse spinal cord tissue lysate Lane 2 : abAB308613 IP in Mouse spinal cord tissue lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab308613 in Mouse spinal cord tissue lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 41 seconds Input is non-boiled as boiling may cause protein aggregates.
All lanes:
Immunoprecipitation - Anti-CX3CR1 antibody [EPR24267-2] (<a href='/en-us/products/primary-antibodies/cx3cr1-antibody-epr24267-2-ab308613'>ab308613</a>) at 1/30 dilution
All lanes:
Mouse spinal cord tissue lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 36 kDa
false
Exposure time: 41s
- WB
Supplier Data
Western blot - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
This data was developed using 308613, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Negative control : Skeletal muscle (PMID : 12881312). Lanes 4-5 of the blot were freshly made and used for Western blotting immediately to minimize protein degradation. Samples are non-boiled as boiling may cause protein aggregation. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-CX3CR1 antibody [EPR24267-2] (<a href='/en-us/products/primary-antibodies/cx3cr1-antibody-epr24267-2-ab308613'>ab308613</a>) at 1/1000 dilution
Lanes 1 and 4:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse spinal cord tissue lysate at 20 µg
Lane 3:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 5:
Rat brain tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 40 kDa
Observed band size: 36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-CX3CR1 antibody [EPR24267-2] - BSA and Azide free (AB308614)
This data was developed using ab308613, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Samples are non-boiled as boiling may cause protein aggregation. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Cx3cr1-KO homozygous mice (Strain ID : T006121).
All lanes:
Western blot - Anti-CX3CR1 antibody [EPR24267-2] (<a href='/en-us/products/primary-antibodies/cx3cr1-antibody-epr24267-2-ab308613'>ab308613</a>) at 1/1000 dilution
Lane 1:
Wild-type mouse brain tissue lysate (male) at 20 µg
Lane 2:
Cx3cr1 knockout mouse brain tissue lysate (male case1) at 20 µg
Lane 3:
Cx3cr1 knockout mouse brain tissue lysate (male case2) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 36 kDa
false
Exposure time: 180s
Related conjugates and formulations (8)
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Anti-CX3CR1 antibody [EPR24267-2]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-CX3CR1 antibody [EPR24267-2]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-CX3CR1 antibody [EPR24267-2]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-CX3CR1 antibody [EPR24267-2]
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660 APC
APC Anti-CX3CR1 antibody [EPR24267-2]
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578 PE
PE Anti-CX3CR1 antibody [EPR24267-2]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-CX3CR1 antibody [EPR24267-2]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-CX3CR1 antibody [EPR24267-2]
Reactivity data
Product details
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
CX3CR1 plays a significant role in immune regulation and cellular migration. It is not part of a larger protein complex but interacts directly with monocyte and microglia cells influencing their activity. CX3CR1 is recognized as a marker for microglia in flow cytometry applications assisting in the identification of these brain-resident immune cells. The receptor is frequently studied using monoclonal antibodies like anti-CX3CR1 and is subject to inhibition by CX3CR1 antagonists such as 8e10 affecting its function in immune responses.
Pathways
CX3CR1 involves itself heavily in the chemokine signaling pathway and the inflammatory response pathway. Its interaction with CX3CL1 influences the PI3K-Akt signaling pathway modulating cell survival and proliferation. The receptor works in conjunction with CCR2 in monocyte navigation impacting the inflammatory cascade during immune response. Their coordinated action is important for cellular trafficking to sites requiring immune intervention.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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