Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
R&D Systems | Catalog # MAB3651
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Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Gln25-Arg339 (Ser199Asn)
Accession # P78423
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
Detection of CX3CL1/Fractalkine by Flow Cytometry
CX3CL1 expression and regulation in human and murine ovarian cancer cell lines. OV-MZ-6 cells (A, B), OVCAR-3 cells (C), or ID8-Trp53−/− cells (D) were stimulated for 24 h ± TNF-alpha (50 ng/mL) and ± TAPI-2 (50 µM) or ± GI254 (5 µM) or the corresponding solvent controls as indicated. Bar graphs on the left show soluble CX3CL1 in cell supernatant measured after 24 h by ELISA (mean ± SEM). The plots on the right show membrane-bound CX3CL1 as determined via FACS analysis. B, Immunocytochemical staining of CX3CL1 in OV-MZ-6 cells stimulated with or without TNF-alpha in the presence or absence of TAPI-2, visualised by confocal laser scanning microscopy (CLSM) using an Alexa 488-conjugated secondary antibody. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39862711), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of CX3CL1/Fractalkine by Flow Cytometry
CX3CL1 expression and regulation in human and murine ovarian cancer cell lines. OV-MZ-6 cells (A, B), OVCAR-3 cells (C), or ID8-Trp53−/− cells (D) were stimulated for 24 h ± TNF-alpha (50 ng/mL) and ± TAPI-2 (50 µM) or ± GI254 (5 µM) or the corresponding solvent controls as indicated. Bar graphs on the left show soluble CX3CL1 in cell supernatant measured after 24 h by ELISA (mean ± SEM). The plots on the right show membrane-bound CX3CL1 as determined via FACS analysis. B, Immunocytochemical staining of CX3CL1 in OV-MZ-6 cells stimulated with or without TNF-alpha in the presence or absence of TAPI-2, visualised by confocal laser scanning microscopy (CLSM) using an Alexa 488-conjugated secondary antibody. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39862711), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of CX3CL1/Fractalkine by Flow Cytometry
CX3CL1 expression and regulation in human and murine ovarian cancer cell lines. OV-MZ-6 cells (A, B), OVCAR-3 cells (C), or ID8-Trp53−/− cells (D) were stimulated for 24 h ± TNF-alpha (50 ng/mL) and ± TAPI-2 (50 µM) or ± GI254 (5 µM) or the corresponding solvent controls as indicated. Bar graphs on the left show soluble CX3CL1 in cell supernatant measured after 24 h by ELISA (mean ± SEM). The plots on the right show membrane-bound CX3CL1 as determined via FACS analysis. B, Immunocytochemical staining of CX3CL1 in OV-MZ-6 cells stimulated with or without TNF-alpha in the presence or absence of TAPI-2, visualised by confocal laser scanning microscopy (CLSM) using an Alexa 488-conjugated secondary antibody. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39862711), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human Alzheimer's disease brain
Western Blot
Sample: Recombinant Human CX3CL1/Fractalkine Full Length (Catalog # 365-FR)
Reviewed Applications
Read 2 reviews rated 5 using MAB3651 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: CX3CL1/Fractalkine
Alternate Names
Gene Symbol
UniProt
Additional CX3CL1/Fractalkine Products
Product Documents for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
For research use only
Related Research Areas
Citations for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513)
Customer Reviews for Human CX3CL1/Fractalkine Chemokine Domain Antibody (81513) (2)
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Customer Images
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Application: ImmunohistochemistrySample Tested: Lymphatic endotheliumSpecies: HumanVerified Customer | Posted 08/30/2021
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Application: ImmunofluorescenceSample Tested: Human HEC1A cellsSpecies: HumanVerified Customer | Posted 01/18/2016HEC1A epithelial cells stained with CX3CL1 and an anti-mouse IgG AlexaFluor 488 secondary
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars