CXCL11 Antibodies

Background

CXCL11 is a small molecule chemokine mainly produced by interferon induction, belonging to the C-X-C subfamily. The protein encoded by this gene specifically binds to the receptor CXCR3, directing activated T cells and natural killer cells to the inflammatory or infected sites, thereby playing a crucial role in immune defense, autoimmune diseases, and anti-tumor responses. It was first identified in 1999, and the three-dimensional structure analysis revealed the typical chemokine folding pattern, providing an important model for understanding the interaction mechanism between chemokines and receptors. Due to its core function in inflammation regulation and shaping of the immune microenvironment, CXCL11 has become an important target for the treatment of autoimmune diseases and cancer immunotherapy research.

Structure Function Application Advantage Our Products

Structure of CXCL11

CXCL11 is a small chemotactic factor protein with a molecular weight of approximately 8.4 kDa. There are slight differences in its molecular weight among different species, mainly due to minor variations in the amino acid sequence.

Species Human Mouse Rat
Molecular Weight (kDa) 8.4 8.3 8.2
Primary Structural Differences The core ELR motif is absent, and it contains multiple basic amino acid residues. Highly homologous to the human sequence and with conserved function There are slight differences in the N-terminal signal peptide region.

This protein is typically composed of 73 amino acid residues (in its mature peptide form) and folds into a compact three-dimensional structure consisting of antiparallel β-sheet and C-terminal α-helix. Its core region contains a conserved three-dimensional fold stabilized by disulfide bonds (e.g., Cys9-Cys50), which is crucial for maintaining structural stability and receptor binding. The "ELR" motif at the N-terminus (actually "DLR" in CXCL11) is a key site for recognizing and binding to its specific receptor CXCR3, while the region rich in basic amino acids near the C-terminus is responsible for interacting with glycosaminoglycans on the cell surface, thereby anchoring the chemokine to the cell surface or extracellular matrix, forming a concentration gradient.

Fig. 1 CXCL11 Promotes HCC Metastasis Through circUBAP2/miR-4756/IFIT1/3 Axis.Fig. 1 CXCL11 Promotes HCC Metastasis Through circUBAP2/miR-4756/IFIT1/3 Axis.1

Key structural properties of CXCL11:

  • Conservative folding of the chemokine (antiparallel β-sheet and C-terminal α-helix)
  • Core structure through the disulfide bond (Cys9 - Cys50) stability
  • The N-terminal contains the "DLR" motif that specifically binds to the CXCR3 receptor

Functions of CXCL11

The main function of CXCL11 is to act as a chemokine, specifically recruiting immune cells to the sites of inflammation or infection. At the same time, it also participates in regulating processes such as the tumor microenvironment, autoimmune responses, and angiogenesis.

Function Description
Immune cell chemotaxis By binding to the receptor CXCR3, it specifically recruits activated Th1 cells, cytotoxic T cells, and natural killer cells.
Anti-tumor immunity Recruit effector immune cells in the tumor microenvironment to enhance the recognition and elimination of cancer cells.
Inflammation Regulation It mediates the local aggregation of inflammatory cells at sites of infection or autoimmune diseases, participating in immune defense and pathological damage.
Vascularization Regulation It can inhibit the migration of vascular endothelial cells through the CXCR3 signaling pathway, thereby affecting pathological vascularization.
Antiviral Response It is strongly induced by interferon in the early stage of viral infection, promoting the localization and activation of adaptive immune cells.

Similar to many chemokines, the functional expression of CXCL11 depends on the concentration gradient formed in the tissue. However, its binding affinity to the CXCR3 receptor is usually higher than that of other ligands in the same family (such as CXCL9 and CXCL10), which enables it to play a more precise regulatory role in specific immune responses.

Applications of CXCL11 and CXCL11 Antibody in Literature

1. Liu, Gao, et al. "Cancer-associated fibroblast-derived CXCL11 modulates hepatocellular carcinoma cell migration and tumor metastasis through the circUBAP2/miR-4756/IFIT1/3 axis." Cell death & disease 12.3 (2021): 260. https://doi.org/10.1038/s41419-021-03545-7

Studies have found that liver cancer-related fibroblasts activate the circUBAP2/miR-4756/IFIT1/3 axis by hypersecreting CXCL11, promoting the expression of IL-17/IL-1β, thereby driving the migration and metastasis of liver cancer. Blocking this pathway can inhibit tumor progression.

2. Zhang, Menghan, et al. "Gut microbial metabolite butyrate suppresses hepatocellular carcinoma growth via CXCL11-dependent enhancement of natural killer cell infiltration." Gut Microbes 17.1 (2025): 2519706. https://doi.org/10.1080/19490976.2025.2519706

Research has found that butyrate, a metabolic product of the gut microbiota, upregulates the expression of CXCL11 in tumor cells through epigenetic remodeling, thereby promoting NK cell infiltration, enhancing their anti-tumor function and improving the prognosis of liver cancer patients.

3. Gil, Christian Martin, et al. "Myostatin and CXCL11 promote nervous tissue macrophages to maintain osteoarthritis pain." Brain, behavior, and immunity 116 (2024): 203-215. https://doi.org/10.1016/j.bbi.2023.12.004

Research has found that CXCL11 and myostatin mediate the persistence of osteoarthritis pain. CXCL11 promotes the aggregation of macrophages in the dorsal root ganglion, and myostatin drives their M1 polarization. Blocking any pathway can relieve pain and reveal a new mechanism of neuroimmune interaction.

4. Li, Yang, et al. "CXCL11 correlates with immune infiltration and impacts patient immunotherapy efficacy: A pan-cancer analysis." Frontiers in immunology 13 (2022): 951247. https://doi.org/10.3389/fimmu.2022.951247

Research has found that CXCL11 is highly expressed in most tumors and is significantly correlated with CD8+ T cell infiltration and immune pathways. Its expression level is associated with biomarkers such as tumor mutational burden, suggesting that it can serve as a potential biomarker for pan-cancer prognosis and immunotherapy.

5. Cao, Yingying, et al. "CXCL11 correlates with antitumor immunity and an improved prognosis in colon cancer." Frontiers in cell and developmental biology 9 (2021): 646252. https://doi.org/10.3389/fcell.2021.646252

Research has found that CXCL11 is highly expressed in colorectal cancer tissues, especially in colon cancer, and is associated with prolonged survival of patients. Its expression promotes the infiltration of anti-tumor immune cells and is positively correlated with cytotoxic genes and PD-L1, making it an independent prognostic biomarker.

Creative Biolabs: CXCL11 Antibodies for Research

Creative Biolabs specializes in the production of high-quality CXCL11 antibodies for research and industrial applications. Our portfolio includes monoclonal antibodies tailored for ELISA, Flow Cytometry, Western blot, immunohistochemistry, and other diagnostic methodologies.

  • Custom CXCL11 Antibody Development: Tailor-made solutions to meet specific research requirements.
  • Bulk Production: Large-scale antibody manufacturing for industry partners.
  • Technical Support: Expert consultation for protocol optimization and troubleshooting.
  • Aliquoting Services: Conveniently sized aliquots for long-term storage and consistent experimental outcomes.

For more details on our CXCL11 antibodies, custom preparations, or technical support, contact us at email.

Reference

  1. Liu, Gao, et al. "Cancer-associated fibroblast-derived CXCL11 modulates hepatocellular carcinoma cell migration and tumor metastasis through the circUBAP2/miR-4756/IFIT1/3 axis." Cell death & disease 12.3 (2021): 260. https://doi.org/10.1038/s41419-021-03545-7
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Anti-CXCL11 antibodies

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Target: CXCL11
Host: Rat
Antibody Isotype: IgG2
Specificity: Mouse
Clone: C11356
Application*: WB, N
Functional Assay
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG1
Specificity: Human
Clone: CBXC-2317
Application*: E, WB
Target: CXCL11
Host: Rat
Antibody Isotype: IgG2a
Specificity: Mouse
Clone: CBXC-1492
Application*: N, WB, E, IH
Functional Assay
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG1
Specificity: Human
Clone: CBXC-2347
Application*: WB, P, F, E, N
Functional Assay
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG2a
Specificity: Human
Clone: CBYY-C2348
Application*: E
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG1
Specificity: Human
Clone: CBYY-C2347
Application*: P
Target: CXCL11
Host: Rat
Antibody Isotype: IgG2a
Specificity: Mouse
Clone: CBFYC-2498
Application*: E, WB
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG1
Specificity: Human
Clone: CBFYC-2497
Application*: E
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG2a, λ
Specificity: Human
Clone: CBFYC-0452
Application*: E
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human
Clone: CBFYC-0196
Application*: E
Target: CXCL11
Host: Mouse
Antibody Isotype: IgG2b, κ
Specificity: Human
Clone: 3D9
Application*: E
More Infomation
Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized) Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized)
For Research Use Only. Not For Clinical Use.
(P): Predicted
* Abbreviations
  • AActivation
  • AGAgonist
  • APApoptosis
  • BBlocking
  • BABioassay
  • BIBioimaging
  • CImmunohistochemistry-Frozen Sections
  • CIChromatin Immunoprecipitation
  • CTCytotoxicity
  • CSCostimulation
  • DDepletion
  • DBDot Blot
  • EELISA
  • ECELISA(Cap)
  • EDELISA(Det)
  • ESELISpot
  • EMElectron Microscopy
  • FFlow Cytometry
  • FNFunction Assay
  • GSGel Supershift
  • IInhibition
  • IAEnzyme Immunoassay
  • ICImmunocytochemistry
  • IDImmunodiffusion
  • IEImmunoelectrophoresis
  • IFImmunofluorescence
  • IGImmunochromatography
  • IHImmunohistochemistry
  • IMImmunomicroscopy
  • IOImmunoassay
  • IPImmunoprecipitation
  • ISIntracellular Staining for Flow Cytometry
  • LALuminex Assay
  • LFLateral Flow Immunoassay
  • MMicroarray
  • MCMass Cytometry/CyTOF
  • MDMeDIP
  • MSElectrophoretic Mobility Shift Assay
  • NNeutralization
  • PImmunohistologyp-Paraffin Sections
  • PAPeptide Array
  • PEPeptide ELISA
  • PLProximity Ligation Assay
  • RRadioimmunoassay
  • SStimulation
  • SESandwich ELISA
  • SHIn situ hybridization
  • TCTissue Culture
  • WBWestern Blot
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