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Rabbit Anti-CCR2 Recombinant Antibody (CBYY-C1131) (CBMAB-C2568-YY)

This product is rabbit antibody that recognizes CCR2. The antibody CBYY-C1131 can be used for immunoassay techniques such as: FC, ICC, IHC, IP
See all CCR2 antibodies

Summary

Host Animal
Rabbit
Specificity
Human, Mouse
Clone
CBYY-C1131
Antibody Isotype
IgG
Application
FC, ICC, IHC, IP

Basic Information

Immunogen
A synthetic peptide corresponding to the N-terminal residues of the human C-C chemokine receptor type 2. MW: 42-52kD
Specificity
Human, Mouse
Antibody Isotype
IgG
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
Tissue culture supernatant
Preservative
0.15M NaCl
Concentration
Liquid
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-C Motif Chemokine Receptor 2
Entrez Gene ID
Human729230
Mouse12772
UniProt ID
HumanP41597
MouseP51683
Function
Key functional receptor for CCL2 but can also bind CCL7 and CCL12 (PubMed:8146186, PubMed:8048929, PubMed:23408426).
Its binding with CCL2 on monocytes and macrophages mediates chemotaxis and migration induction through the activation of the PI3K cascade, the small G protein Rac and lamellipodium protrusion (Probable). Also acts as a receptor for the beta-defensin DEFB106A/DEFB106B (PubMed:23938203).
Regulates the expression of T-cell inflammatory cytokines and T-cell differentiation, promoting the differentiation of T-cells into T-helper 17 cells (Th17) during inflammation (By similarity).
Facilitates the export of mature thymocytes by enhancing directional movement of thymocytes to sphingosine-1-phosphate stimulation and up-regulation of S1P1R expression; signals through the JAK-STAT pathway to regulate FOXO1 activity leading to an increased expression of S1P1R (By similarity).
Plays an important role in mediating peripheral nerve injury-induced neuropathic pain (By similarity).
Increases NMDA-mediated synaptic transmission in both dopamine D1 and D2 receptor-containing neurons, which may be caused by MAPK/ERK-dependent phosphorylation of GRIN2B/NMDAR2B (By similarity).
Mediates the recruitment of macrophages and monocytes to the injury site following brain injury (By similarity).
(Microbial infection) Alternative coreceptor with CD4 for HIV-1 infection.
Biological Process
Blood vessel remodeling Source: BHF-UCL
Calcium-mediated signaling Source: GO_Central
Cell chemotaxis Source: GO_Central
Cellular calcium ion homeostasis Source: BHF-UCL
Cellular defense response Source: ProtInc
Cellular homeostasis Source: BHF-UCL
Chemokine-mediated signaling pathway Source: BHF-UCL
Chemotaxis Source: ProtInc
Cytokine-mediated signaling pathway Source: MGI
Dendritic cell chemotaxis Source: BHF-UCL
G protein-coupled receptor signaling pathway Source: Reactome
Immune response Source: GO_Central
Inflammatory response Source: GO_Central
Inflammatory response to wounding Source: UniProtKB
Macrophage migration Source: UniProtKB
Monocyte extravasation Source: UniProtKB
Negative regulation of adenylate cyclase activity Source: ProtInc
Negative regulation of angiogenesis Source: BHF-UCL
Negative regulation of eosinophil degranulation Source: BHF-UCL
Negative regulation of type 2 immune response Source: BHF-UCL
Positive regulation of alpha-beta T cell proliferation Source: BHF-UCL
Positive regulation of astrocyte chemotaxis Source: BHF-UCL
Positive regulation of CD8-positive, alpha-beta T cell extravasation Source: BHF-UCL
Positive regulation of cold-induced thermogenesis Source: YuBioLab
Positive regulation of cytosolic calcium ion concentration Source: GO_Central
Positive regulation of hematopoietic stem cell migration Source: BHF-UCL
Positive regulation of immune complex clearance by monocytes and macrophages Source: BHF-UCL
Positive regulation of inflammatory response Source: BHF-UCL
Positive regulation of interferon-gamma production Source: BHF-UCL
Positive regulation of interleukin-2 production Source: BHF-UCL
Positive regulation of monocyte chemotaxis Source: UniProtKB
Positive regulation of monocyte extravasation Source: BHF-UCL
Positive regulation of NMDA glutamate receptor activity Source: ARUK-UCL
Positive regulation of synaptic transmission, glutamatergic Source: UniProtKB
Positive regulation of T cell activation Source: BHF-UCL
Positive regulation of T cell chemotaxis Source: BHF-UCL
Positive regulation of T-helper 1 type immune response Source: BHF-UCL
Positive regulation of thymocyte migration Source: UniProtKB
Positive regulation of tumor necrosis factor production Source: BHF-UCL
Receptor signaling pathway via JAK-STAT Source: ProtInc
Regulation of inflammatory response Source: UniProtKB
Regulation of T cell cytokine production Source: UniProtKB
Regulation of T cell differentiation Source: UniProtKB
Regulation of vascular endothelial growth factor production Source: BHF-UCL
Response to wounding Source: ProtInc
Sensory perception of pain Source: UniProtKB
T-helper 17 cell chemotaxis Source: BHF-UCL
Viral process Source: UniProtKB-KW
Cellular Location
Cell membrane. The chemoattractant receptors are distributed throughout the cell surface; after stimulation with a ligand, such as CCL2, they are rapidly recruited into microdomain clusters at the cell membrane.
Topology
Extracellular: 1-42
Helical: 43-70
Cytoplasmic: 71-80
Helical: 81-100
Extracellular: 101-114
Helical: 115-136
Cytoplasmic: 137-153
Helical: 154-178
Extracellular: 179-206
Helical: 207-226
Cytoplasmic: 227-243
Helical: 244-268
Extracellular: 269-285
Helical: 286-309
Cytoplasmic: 310-374
PTM
N-glycosylated.
Sulfation increases the affinity for both monomeric and dimeric CCL2 with stronger binding to the monomeric form (PubMed:11046064, PubMed:23408426). Binding of sulfated CCR2 to CCL2 promotes conversion of CCL2 from dimer to monomer (PubMed:11046064, PubMed:23408426).

Brody, S. L., Gunsten, S. P., Luehmann, H. P., Sultan, D. H., Hoelscher, M., Heo, G. S., ... & Liu, Y. (2021). Chemokine Receptor 2–targeted Molecular Imaging in Pulmonary Fibrosis. A Clinical Trial. American journal of respiratory and critical care medicine, 203(1), 78-89.

Zhu, S., Liu, M., Bennett, S., Wang, Z., Pfleger, K. D., & Xu, J. (2021). The molecular structure and role of CCL2 (MCP‐1) and C‐C chemokine receptor CCR2 in skeletal biology and diseases. Journal of Cellular Physiology.

Figueiredo, A. F. A., Wnuk, N. T., Vieira, C. P., Gonçalves, M. F. F., Brener, M. R. G., Diniz, A. B., ... & Costa, G. M. J. (2021). Activation of C–C motif chemokine receptor 2 modulates testicular macrophages number, steroidogenesis, and spermatogenesis progression. Cell and Tissue Research, 386(1), 173-190.

Zhang, X., Detering, L., Sultan, D., Luehmann, H., Li, L., Heo, G. S., ... & Liu, Y. (2021). CC chemokine receptor 2-targeting copper nanoparticles for positron emission tomography-guided delivery of gemcitabine for pancreatic ductal adenocarcinoma. ACS nano, 15(1), 1186-1198.

Iwamoto, H., Izumi, K., & Mizokami, A. (2020). Is the CC Motif Ligand 2–CC Chemokine Receptor 2 Axis a Promising Target for Cancer Therapy and Diagnosis?. International Journal of Molecular Sciences, 21(23), 9328.

Santos, A. G. A., Pereira, L. A. A. C., Viana, J. H. M., Russo, R. C., & Campos-Junior, P. H. A. (2020). The CC-chemokine receptor 2 is involved in the control of ovarian folliculogenesis and fertility lifespan in mice. Journal of Reproductive Immunology, 141, 103174.

Yumimoto, K., Sugiyama, S., Mimori, K., & Nakayama, K. I. (2019). Potentials of C‐C motif chemokine 2–C‐C chemokine receptor type 2 blockers including propagermanium as anticancer agents. Cancer science, 110(7), 2090-2099.

Rojo, J. L., Jaworski, J. P., & Peluffo, M. C. (2019). Direct role of the CC motif chemokine receptor 2/monocyte chemoattractant protein 1 system in the feline cumulus oocyte complex. Biology of reproduction, 100(4), 1046-1056.

Parker, R., Weston, C. J., Miao, Z., Corbett, C., Armstrong, M. J., Ertl, L., ... & Adams, D. H. (2018). CC chemokine receptor 2 promotes recruitment of myeloid cells associated with insulin resistance in nonalcoholic fatty liver disease. American Journal of Physiology-Gastrointestinal and Liver Physiology, 314(4), G483-G493.

Guo, Y. C., Zhang, M., Wang, F. X., Pei, G. C., Sun, F., Zhang, Y., ... & Wang, C. Y. (2017). Macrophages Regulate Unilateral Ureteral Obstruction-Induced Renal Lymphangiogenesis Through CC Motif Chemokine Receptor 2–Dependent Phosphatidylinositol 3-Kinase-Akt–Mechanistic Target Of Rapamycin Signaling and Hypoxia-Inducible Factor-1α/Vascular Endothelial Growth Factor-C Expression. The American journal of pathology, 187(8), 1736-1749.

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

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