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CD209 encodes a transmembrane receptor and is often referred to as DC-SIGN because of its expression on the surface of dendritic cells and macrophages. Additionally we are shipping CD209 Molecule Proteins (18) and CD209 Molecule Kits (7) and many more products for this protein.
Showing 10 out of 483 products:
Human Monoclonal CD209 Primary Antibody for FACS - ABIN4898513
Li, Xia, Liu, Wang, Dai, Wang, Zheng, Chen, Li, Abudumijiti, Zhou, Wang, Lu, Zhu, Yang, Zhang, Yin, Wang, Zhou, Lu, Zhou, Guo: Protective effects of astaxanthin on ConA-induced autoimmune hepatitis by the JNK/p-JNK pathway-mediated inhibition of autophagy and apoptosis. in PLoS ONE 2015
Show all 7 references for 4898513
Human Monoclonal CD209 Primary Antibody for FACS, IHC - ABIN4900749
Wu, Bashirova, Martin, Villamide, Mehlhop, Chertov, Unutmaz, Pope, Carrington, KewalRamani: Rhesus macaque dendritic cells efficiently transmit primate lentiviruses independently of DC-SIGN. in Proceedings of the National Academy of Sciences of the United States of America 2002
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Human Monoclonal CD209 Primary Antibody for FACS - ABIN4898517
Gautam, Carter, Katz, Butler, Barnes, Hasegawa, Ratterree, Silvestri, Marx, Hirsch, Pandrea, Apetrei: In vitro characterization of primary SIVsmm isolates belonging to different lineages. In vitro growth on rhesus macaque cells is not predictive for in vivo replication in rhesus macaques. in Virology 2007
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Human Polyclonal CD209 Primary Antibody for WB - ABIN871703
Engering, Geijtenbeek, van Vliet, Wijers, van Liempt, Demaurex, Lanzavecchia, Fransen, Figdor, Piguet, van Kooyk: The dendritic cell-specific adhesion receptor DC-SIGN internalizes antigen for presentation to T cells. in Journal of immunology (Baltimore, Md. : 1950) 2002
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Human Monoclonal CD209 Primary Antibody for FACS - ABIN4898509
Rodriguez-Garcia, Shen, Barr, Boesch, Ackerman, Kappes, Ochsenbauer, Wira: Dendritic cells from the human female reproductive tract rapidly capture and respond to HIV. in Mucosal immunology 2016
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Human Monoclonal CD209 Primary Antibody for FACS - ABIN181973
Relloso, Puig-Kröger, Pello, Rodríguez-Fernández, de la Rosa, Longo, Navarro, Muñoz-Fernández, Sánchez-Mateos, Corbí: DC-SIGN (CD209) expression is IL-4 dependent and is negatively regulated by IFN, TGF-beta, and anti-inflammatory agents. in Journal of immunology (Baltimore, Md. : 1950) 2002
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Human Monoclonal CD209 Primary Antibody for FACS - ABIN320225
Melero, Gabari, Corbí, Relloso, Mazzolini, Schmitz, Rodriguez-Calvillo, Tirapu, Camafeita, Albar, Prieto: An anti-ICAM-2 (CD102) monoclonal antibody induces immune-mediated regressions of transplanted ICAM-2-negative colon carcinomas. in Cancer research 2002
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Human Monoclonal CD209 Primary Antibody for FACS, IF - ABIN1106050
Khoo, Chan, Chan, Lin: DC-SIGN and L-SIGN: the SIGNs for infection. in Journal of molecular medicine (Berlin, Germany) 2008
The development and use of CD209 to characterize the phenotype of CD209 expressing cells in bovine blood using flow cytometry is reported.
a DC-SIGN-like molecule expressed specifically by bovine DC. This molecule may play an important role in the infection of bovine (DC) cells with M. bovis.
The cloning and characterization of the cDNA and gene encoding porcine DC-SIGN (pDC (show PDC Antibodies)-SIGN)is reported. The results will help better understand the biological role(s) of DC-SIGN family in innate immunity during the evolutionary process.
identification and functional characterization of DC-SIGN/CD209 molecule in zebrafish
CD209 polymorphisms could play a role in the susceptibility to Hepatitis C infection as well as interferon (show IFNA Antibodies) treatment response
The activation of B cells enhances DC-SIGN expression and promotes susceptibility of B cells to the avian H5N1 infection.
Binding of common allergens by DC-SIGN on DCs may initiate allergen sensitization of atopic dermatitis or provoke the relapse of atopic dermatitis
These results suggest that DC-SIGN may be an alternative receptor for influenza A(H1N1)pdm09 virus.
the neck domains of DC-SIGN and DC-SIGNR (show CLEC4M Antibodies) can contribute to the different functions of these receptors by presenting the sugar-binding sites in different contexts.
The results demonstrate that DC-SIGN among the many hGBP expressed by DCs binds to alpha-fucosylated HMGs (show HMGCS2 Antibodies), and suggest that such interactions may be important in influencing immune responses in the developing infant.
Together, these studies confirm a role for C-type lectin (show MBL2 Antibodies) receptors DC-SIGN and L-SIGN (show CLEC4M Antibodies) as attachment factors and entry receptors for human metapneumovirus infection.
DC-SIGNR (show CLEC4M Antibodies) VNTR and DC-SIGN VNTR, were not associated with the risk of pulmonary tuberculosis in a sample of Iranian population
CD209 gene -871A/G is associated with decreased susceptibility to pulmonary tuberculosis (PT) overall; -336A/G polymorphism is associated with increased susceptibility in Asians and -139G/A polymorphism is not associated with susceptibility to PT
The high-mannose N-linked glycan at N154 of Japanese encephalitis virus E glycoprotein was shown to be crucial for binding to DC-SIGN and subsequent internalization.
DC-SIGN+ cells showed a clear differential distribution in the decidua in the first 2 weeks of pregnancy, being found only adjacent to the implantation site
DC-SIGN expression in mesenteric lymph nodes is significantly downregulated in simian immunodeficiency virus-infected pig-tailed macaques.
results suggested that podocytes in lupus nephritis can exert dendritic cell-like function through their expression of DC-SIGN, which may be involved in immune and inflammatory responses of renal tissues
High-resolution crystal structures of the SIGN-R1 carbohydrate recognition domain show 2 binding sites allowing SIGNR1 (show CD209B Antibodies) to simultaneously bind both immune glycoproteins and microbial polysaccharide components.
Data suggest that serum amyloid P (SAP (show APCS Antibodies)) activates CD209 DC-SIGN to regulate the innate immune system differently from C-reactive protein (CRP (show CRP Antibodies)), and that DC-SIGN is a target for antifibrotics.
Intestinal enterocytes regulate tissue-associated immune compartments under the control of DC-SIGN in inflammatory bowel disease.
In vivo T cell activation induces the formation of CD209(+) PDL-2 (show PDCD1LG2 Antibodies)(+) dendritic cells.
CD209a expression on dendritic cells is critical for the development of pathogenic Th17 cell responses in murine schistosomiasis.
CD209a is activated in macrophages by LECT2 (show LECT2 Antibodies).
The neck region of the C-type lectin DC-SIGN regulates its surface spatiotemporal organization and virus-binding capacity on antigen-presenting cells
interactions between the CRD (show CRX Antibodies) of DC-SIGN and the extracellular matrix and/or cis (show CISH Antibodies) interactions with transmembrane scaffolding protein(s) play an essential role in organizing these microdomains
analysis of activated apoptotic cells induce dendritic cell maturation via engagement of Toll-like receptor 4 (TLR4 (show TLR4 Antibodies)), dendritic cell-specific intercellular adhesion molecule 3 (ICAM-3 (show ICAM3 Antibodies))-grabbing nonintegrin (DC-SIGN), and beta2 integrins
This gene encodes a transmembrane receptor and is often referred to as DC-SIGN because of its expression on the surface of dendritic cells and macrophages. The encoded protein is involved in the innate immune system and recognizes numerous evolutionarily divergent pathogens ranging from parasites to viruses with a large impact on public health. The protein is organized into three distinct domains: an N-terminal transmembrane domain, a tandem-repeat neck domain and C-type lectin carbohydrate recognition domain. The extracellular region consisting of the C-type lectin and neck domains has a dual function as a pathogen recognition receptor and a cell adhesion receptor by binding carbohydrate ligands on the surface of microbes and endogenous cells. The neck region is important for homo-oligomerization which allows the receptor to bind multivalent ligands with high avidity. Variations in the number of 23 amino acid repeats in the neck domain of this protein are rare but have a significant impact on ligand binding ability. This gene is closely related in terms of both sequence and function to a neighboring gene (GeneID 10332\; often referred to as L-SIGN). DC-SIGN and L-SIGN differ in their ligand-binding properties and distribution. Alternative splicing results in multiple variants.
, CD209-like protein
, C-type lectin domain family 4, member M
, DC-SIGN protein
, C-type lectin domain family 4 member L
, C-type lectin domain family 4, member L
, HIV gpl20-binding protein
, dendritic cell-specific ICAM-3-grabbing non-integrin 1
, dendritic cell-specific intracellular adhesion molecules (ICAM)-3 grabbing non-integrin
, dendritic cell-specific ICAM-3 grabbing non-integrin
, putative mannose-binding C-type lectin
, CD209 antigen-like protein A
, dendritic cell-specific ICAM-3-grabbing non-integrin
, CD209 antigen-like protein C
, CD209c antigen