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Mouse Anti-CXCL12 Recombinant Antibody (CBXC-1319) (CBMAB-C1586-CQ)


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Summary

Host Animal
Mouse
Specificity
Human, Mouse
Clone
CBXC-1319
Antibody Isotype
IgG1
Application
FC

Basic Information

Specificity
Human, Mouse
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Concentration
0.2 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
C-X-C Motif Chemokine Ligand 12
Introduction
CXCL12 (C-X-C Motif Chemokine Ligand 12) is a Protein Coding gene. Diseases associated with CXCL12 include Human Immunodeficiency Virus Type 1 and Aids Dementia Complex. Among its related pathways are Apoptotic Pathways in Synovial Fibroblasts and PAK Pathway. Gene Ontology (GO) annotations related to this gene include receptor binding and chemokine activity.
Entrez Gene ID
Human6387
Mouse20315
UniProt ID
HumanP48061
MouseP40224
Alternative Names
C-X-C Motif Chemokine Ligand 12; Pre-B Cell Growth-Stimulating Factor; Chemokine (C-X-C Motif) Ligand 12; Intercrine Reduced In Hepatomas; Stromal Cell-Derived Factor 1; SDF1; PBSF; IRH; C-X-C Motif Chemokine 12;
Function
Chemoattractant active on T-lymphocytes and monocytes but not neutrophils. Activates the C-X-C chemokine receptor CXCR4 to induce a rapid and transient rise in the level of intracellular calcium ions and chemotaxis. SDF-1-beta(3-72) and SDF-1-alpha(3-67) show a reduced chemotactic activity. Binding to cell surface proteoglycans seems to inhibit formation of SDF-1-alpha(3-67) and thus to preserve activity on local sites. Also binds to atypical chemokine receptor ACKR3, which activates the beta-arrestin pathway and acts as a scavenger receptor for SDF-1. Binds to the allosteric site (site 2) of integrins and activates integrins ITGAV:ITGB3, ITGA4:ITGB1 and ITGA5:ITGB1 in a CXCR4-independent manner (PubMed:29301984).

Acts as a positive regulator of monocyte migration and a negative regulator of monocyte adhesion via the LYN kinase. Stimulates migration of monocytes and T-lymphocytes through its receptors, CXCR4 and ACKR3, and decreases monocyte adherence to surfaces coated with ICAM-1, a ligand for beta-2 integrins. SDF1A/CXCR4 signaling axis inhibits beta-2 integrin LFA-1 mediated adhesion of monocytes to ICAM-1 through LYN kinase. Inhibits CXCR4-mediated infection by T-cell line-adapted HIV-1. Plays a protective role after myocardial infarction. Induces down-regulation and internalization of ACKR3 expressed in various cells. Has several critical functions during embryonic development; required for B-cell lymphopoiesis, myelopoiesis in bone marrow and heart ventricular septum formation. Stimulates the proliferation of bone marrow-derived B-cell progenitors in the presence of IL7 as well as growth of stromal cell-dependent pre-B-cells (By similarity).
Biological Process
Adult locomotory behavior Source: Ensembl
Animal organ regeneration Source: Ensembl
Antimicrobial humoral immune response mediated by antimicrobial peptide Source: UniProtKB
Axon guidance Source: GO_Central
Blood circulation Source: ProtInc
Cell adhesion Source: ProtInc
Cell chemotaxis Source: UniProtKB
Cellular calcium ion homeostasis Source: ProtInc
Cellular response to chemokine Source: BHF-UCL
Chemokine (C-X-C motif) ligand 12 signaling pathway Source: BHF-UCL
Chemokine-mediated signaling pathway Source: BHF-UCL
Chemotaxis Source: UniProtKB
Defense response Source: InterPro
Detection of mechanical stimulus involved in sensory perception of pain Source: Ensembl
Detection of temperature stimulus involved in sensory perception of pain Source: Ensembl
G protein-coupled receptor signaling pathway Source: Reactome
Immune response Source: ProtInc
Induction of positive chemotaxis Source: GO_Central
Integrin activation Source: UniProtKB
Killing of cells of other organism Source: UniProtKB
Negative regulation of dendritic cell apoptotic process Source: BHF-UCL
Negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage Source: BHF-UCL
Negative regulation of leukocyte tethering or rolling Source: UniProtKB
Neuron migration Source: Ensembl
Positive regulation of axon extension involved in axon guidance Source: Ensembl
Positive regulation of calcium ion import Source: BHF-UCL
Positive regulation of cell adhesion Source: MGI
Positive regulation of cell migration Source: GO_Central
Positive regulation of dopamine secretion Source: Ensembl
Positive regulation of endothelial cell proliferation Source: Ensembl
Positive regulation of monocyte chemotaxis Source: UniProtKB
Positive regulation of neuron differentiation Source: Ensembl
Positive regulation of T cell migration Source: MGI
Regulation of actin polymerization or depolymerization Source: ProtInc
Response to heat Source: Ensembl
Response to hypoxia Source: Ensembl
Response to peptide hormone Source: Ensembl
Response to radiation Source: Ensembl
Response to ultrasound Source: Ensembl
Response to virus Source: ProtInc
Signal transduction Source: ProtInc
T cell chemotaxis Source: UniProtKB
Telencephalon cell migration Source: Ensembl
Viral process Source: UniProtKB-KW
Cellular Location
Secreted
PTM
Processed forms SDF-1-beta(3-72) and SDF-1-alpha(3-67) are produced after secretion by proteolytic cleavage of isoforms Beta and Alpha, respectively. The N-terminal processing is probably achieved by DPP4. Isoform Alpha is first cleaved at the C-terminus to yield a SDF-1-alpha(1-67) intermediate before being processed at the N-terminus. The C-terminal processing of isoform Alpha is reduced by binding to heparin and, probably, cell surface proteoglycans.
More Infomation

Guo, J., Tong, C. Y., Shi, J. G., & Li, X. J. (2022). CXC motif chemokine ligand 12 (CXCL12)/CXC motif chemokine receptor 7 (CXCR7) regulates epithelial-mesenchymal transition process and promotes the metastasis of esophageal cancer by activating signal transducer and activator of transcription 3 (STAT3) pathway. Bioengineered, 13(3), 7425-7438.

Li, D., & Li, Q. (2022). MicroRNA-200b-3p restrains gastric cancer cell proliferation, migration, and invasion via CXC motif chemokine ligand 12/CXC chemokine receptor 7 axis. Bioengineered, 13(3), 6509-6520.

Qin, C., Memon, N. H., Gong, Q., Shi, Q., & Yang, Q. (2021). Diurnal expression of CXC receptors 4 (CXCR4) and CXC chemokine ligand 12 (CXCL12) in Pelteobagrus vachellii. Chronobiology international, 38(9), 1299-1307.

Andrés-Benito, P., Povedano, M., Domínguez, R., Marco, C., Colomina, M. J., López-Pérez, Ó., ... & Ferrer, I. (2020). Increased CXC motif chemokine ligand 12 levels in cerebrospinal fluid as a candidate biomarker in sporadic amyotrophic lateral sclerosis. International Journal of Molecular Sciences, 21(22), 8680.

Shi, Y., Riese, D. J., & Shen, J. (2020). The role of the CXCL12/CXCR4/CXCR7 chemokine axis in cancer. Frontiers in pharmacology, 1969.

Dai, Y., Liu, S., Xie, X., Ding, M., Zhou, Q., & Zhou, X. (2019). MicroRNA‑31 promotes chondrocyte proliferation by targeting C‑X‑C motif chemokine ligand 12. Molecular Medicine Reports, 19(3), 2231-2237.

Zhang, B., Wu, C., Zhang, Z., Yan, K., Li, C., Li, Y., & Li, L. (2019). CXCL12 is associated with FoxP3+ tumor‑infiltrating lymphocytes and affects the survival of patients with oral squamous cell carcinoma. Oncology Letters, 18(2), 1099-1106.

Shen, L., Li, J., Liu, Q., Song, W., Zhang, X., Tiruthani, K., ... & Huang, L. (2018). Local blockade of interleukin 10 and CXC motif chemokine ligand 12 with nano-delivery promotes antitumor response in murine cancers. Acs Nano, 12(10), 9830-9841.

Meng, W., Xue, S., & Chen, Y. (2018). The role of CXCL12 in tumor microenvironment. Gene, 641, 105-110.

Han, J., Jeong, W., Gu, M. J., Yoo, I., Yun, C. H., Kim, J., & Ka, H. (2018). Cysteine-X-cysteine motif chemokine ligand 12 and its receptor CXCR4: expression, regulation, and possible function at the maternal–conceptus interface during early pregnancy in pigs. Biology of Reproduction, 99(6), 1137-1148.

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For research use only. Not intended for any clinical use.

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