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AB89229

Anti-CX3CL1 antibody [MM0207-8J23]

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(5 Publications)

Mouse Monoclonal CX3CL1 antibody. Suitable for WB, IHC-P and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human CX3CL1.

View Alternative Names

FKN, NTT, SCYD1, A-152E5.2, CX3CL1, Fractalkine, C-X3-C motif chemokine 1, CX3C membrane-anchored chemokine, Neurotactin, Small-inducible cytokine D1

1 Images
Western blot - Anti-CX3CL1 antibody [MM0207-8J23] (AB89229)
  • WB

Supplier Data

Western blot - Anti-CX3CL1 antibody [MM0207-8J23] (AB89229)

All lanes:

Western blot - Anti-CX3CL1 antibody [MM0207-8J23] (ab89229) at 1/500 dilution

All lanes:

Human placenta tissue lysate

Predicted band size: 42 kDa

Observed band size: 35 kDa

false

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

MM0207-8J23

Isotype

IgG1

Carrier free

No

Reacts with

Human

Applications

WB, IHC-P

applications

Immunogen

Recombinant Full Length Protein corresponding to Human CX3CL1.

P78423

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/500 - 1/1000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "guaranteed", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein G
Storage buffer
Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

CX3CL1 also known as fractalkine is a chemokine protein characterized mechanically by its dual function as both a chemoattractant and adhesion molecule. It exhibits a unique membrane-bound structure and can exist in a soluble form after proteolytic cleavage. The mass of CX3CL1 is approximately 42-45 kDa. This protein is highly expressed in endothelial cells neurons and tissues with substantial vascularization. Considerable interest surrounds the potential of CX3CL1 assessment in various studies often involving applications like fractalkine ELISA or assays on mouse models.
Biological function summary

CX3CL1 is involved in the immune system and nervous system functions influencing leukocyte adhesion and migration. It is not known to be part of a large multiprotein complex but directly interacts with its fractalkine receptor CX3CR1 on the surface of immune cells. This interaction regulates communication between neurons and microglia which highlights its role in neuroinflammation. CX3CL1's expression and function suggest a significant influence over inflammatory responses and homeostatic balance within these systems.

Pathways

CX3CL1 plays a role in the MAPK and PI3K-Akt pathways vital for cell survival proliferation and migration. Within these pathways CX3CL1 influences and interacts with several proteins thereby modulating inflammatory responses and cellular migration. These pathways are essential for immune system regulation where CX3CL1 acts as a mediator in signal transduction processes that connect immune responses to cellular activities such as proliferation and survival.

CX3CL1 has associations with neurodegenerative disorders like Alzheimer's disease and inflammatory diseases such as rheumatoid arthritis. Alterations in CX3CL1 expression or its fractalkine receptor function can influence disease progression by affecting how immune cells communicate and migrate to inflamed or damaged tissues. CX3CR1 the receptor for CX3CL1 represents an important link in these connections driving research efforts to explore therapies targeting these interactions to alleviate disease symptoms.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Chemokine that acts as a ligand for both CX3CR1 and integrins ITGAV : ITGB3 and ITGA4 : ITGB1 (PubMed : 12055230, PubMed : 21829356, PubMed : 23125415, PubMed : 9782118, PubMed : 9931005). The CX3CR1-CX3CL1 signaling exerts distinct functions in different tissue compartments, such as immune response, inflammation, cell adhesion and chemotaxis (PubMed : 12055230, PubMed : 9024663, PubMed : 9177350, PubMed : 9782118). Regulates leukocyte adhesion and migration processes at the endothelium (PubMed : 9024663, PubMed : 9177350). Can activate integrins in both a CX3CR1-dependent and CX3CR1-independent manner (PubMed : 23125415, PubMed : 24789099). In the presence of CX3CR1, activates integrins by binding to the classical ligand-binding site (site 1) in integrins (PubMed : 23125415, PubMed : 24789099). In the absence of CX3CR1, binds to a second site (site 2) in integrins which is distinct from site 1 and enhances the binding of other integrin ligands to site 1 (PubMed : 23125415, PubMed : 24789099).. Processed fractalkine. The soluble form is chemotactic for T-cells and monocytes, but not for neutrophils.. Fractalkine. The membrane-bound form promotes adhesion of those leukocytes to endothelial cells.. (Microbial infection) Mediates the cytoadherence of erythrocytes infected with parasite P.falciparum (strain 3D7) with endothelial cells by interacting with P.falciparum CBP1 and CBP2 expressed at the surface of erythrocytes (PubMed : 27653778). The adhesion prevents the elimination of infected erythrocytes by the spleen (Probable).
See full target information CX3CL1

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

Cell cycle (Georgetown, Tex.) 21:1697-1709 PubMed35485293

2022

Suppression of CX3CL1 by miR-497-5p inhibits cell growth and invasion through inactivating the ERK/AKT pathway in NSCLC cells.

Applications

Unspecified application

Species

Unspecified reactive species

Wen Tang,Ping Jia,Lin Zuo,Jia Zhao

Neoplasma 69:670-679 PubMed35330998

2022

CX3CL1 in the red bone marrow promotes renal cell carcinoma to metastasize to the spine by involving the Src-related pathway.

Applications

Unspecified application

Species

Unspecified reactive species

An-Nan Hu,Fan-Cheng Chen,Ke-Tao Wang,Zhen-Qing Wang,Yun Liang,Jian Dong

International journal of oncology 57:249-263 PubMed32319605

2020

ADAM17-regulated CX3CL1 expression produced by bone marrow endothelial cells promotes spinal metastasis from hepatocellular carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Chi Sun,Annan Hu,Shengxing Wang,Bo Tian,Libo Jiang,Yun Liang,Houlei Wang,Jian Dong

The European respiratory journal 55: PubMed31744836

2020

CX3CR1-fractalkine axis drives kinetic changes of monocytes in fibrotic interstitial lung diseases.

Applications

Unspecified application

Species

Unspecified reactive species

Flavia R Greiffo,Valeria Viteri-Alvarez,Marion Frankenberger,Daniela Dietel,Almudena Ortega-Gomez,Joyce S Lee,Anne Hilgendorff,Jürgen Behr,Oliver Soehnlein,Oliver Eickelberg,Isis E Fernandez

Clinical cancer research : an official journal of the American Association for Cancer Research 20:3094-106 PubMed24737547

2014

GM-CSF Production by Tumor Cells Is Associated with Improved Survival in Colorectal Cancer.

Applications

Unspecified application

Species

Human

Christian A Nebiker,Junyi Han,Serenella Eppenberger-Castori,Giandomenica Iezzi,Christian Hirt,Francesca Amicarella,Eleonora Cremonesi,Xaver Huber,Elisabetta Padovan,Basilio Angrisani,Raoul A Droeser,Raffaele Rosso,Martin Bolli,Daniel Oertli,Urs von Holzen,Michel Adamina,Manuele G Muraro,Chantal Mengus,Paul Zajac,Giuseppe Sconocchia,Markus Zuber,Luigi Tornillo,Luigi Terracciano,Giulio C Spagnoli
View all publications

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