CD1C Antibody (YA3938)(PBS only)
(Synonyms: R7; CD1; CD1A; BDCA1)CD1C Antibody (YA3938) is a Mouse-derived and non-conjugated IgG2b monoclonal antibody, targeting to CD1C.
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Host:
Mouse
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Isotype:
IgG
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Application:
IHC-P, FC, ELISA
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Reactivity :
Human
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Formulation:
Supplied in PBS, pH 7.4.
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Conjugation:
Non-conjugated
Applications
| Application |
IHC-P
IHC-P: Immunohistochemistry-Paraffin
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FC
FC: Flow Cytometry
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ELISA
ELISA: Enzyme Linked Immunosorbent Assay
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|---|---|---|---|
| Dilution Ratio | 1:200-1:1000 | 1:200-1:400 | 1:10000 |
Product Details
CD1C Antibody (YA3938) is a Mouse-derived and non-conjugated IgG2b monoclonal antibody, targeting to CD1C.
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Host Mouse
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 38 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 38 kDa
Purified recombinant fragment of human CD1C (AA: extra 18-302) expressed in E. Coli.
affinity purified.
Non-conjugated
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS, pH 7.4.
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Background
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Function
CD1c is a group 1 CD1 molecule expressed predominantly by human conventional dendritic cells (cDC2) and functions as a lipid antigen-presenting molecule that activates antigen-specific T-cell responses through presentation of structurally diverse endogenous and microbial lipids[1][2]. Mechanistically, CD1c participates in adaptive immune regulation by presenting mycobacterial lipids, phosphatidylinositol, phosphatidylcholine, sulfatides, and lipopeptide antigens, thereby supporting T-cell activation and interferon-γ production during antimicrobial immune responses[1]. CD1c+ dendritic cells also produce IL-12p70, IL-1β, IL-6, and IL-23 following innate immune stimulation and promote both Th1 and Th17 effector differentiation, linking antigen presentation to inflammatory cytokine networks[3]. In autoimmune and inflammatory settings, activated CD1c+ dendritic cells have been implicated in pathogenic Th1/Th17 immune responses, highlighting their relevance in disease-associated immune activation[3]. Compared with related CD1 isoforms, including CD1a and CD1b, CD1c exhibits distinct structural features that enable presentation of a broader repertoire of lipid-based antigens, supporting functional specialization within the group 1 CD1 family[1][2]. Within the CD1c+ dendritic-cell compartment, CD14+ and CD14− subsets display divergent transcriptional and functional characteristics, with CD14+ populations expressing monocyte-associated markers and showing reduced T-cell stimulatory capacity[4]. Furthermore, CD1c+CD163+ dendritic-cell subsets can prime CD8+CD103+ T cells through TGF-β signaling and are associated with tissue-resident memory T-cell responses in tumor microenvironments, supporting their utility in tumor immunology research models[5].
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Subcellular Localization
Cell membrane; Single-pass type I membrane protein; Endosome membrane; Single-pass type I membrane protein; Lysosome
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Expression
Tissue_specificity:It is expressed in cortical thymocytes, certain T-cell leukemias, and various other tissues. -
Subunit
Heterodimer with B2M (beta-2-microglobulin)
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SwissProt ID
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Synonyms
R7; CD1; CD1A; BDCA1
Documentation
References
[1]. Rabezanahary H, et al. Live virus neutralizing antibodies against pre and post Omicron strains in food and retail workers in Québec, Canada. Heliyon. 2024 May 21;10(10):e31026. [Content Brief]
[2]. Heger L, et al. Subsets of CD1c+ DCs: Dendritic Cell Versus Monocyte Lineage. Front Immunol. 2020 Sep 30;11:559166. [Content Brief]
[3]. Leal Rojas IM, et al. Human blood CD1c+ dendritic cells promote Th1 and Th17 effector function in memory CD4+ T cells. Front Immunol. 2017;8:971. [Content Brief]
[4]. Heger L, et al. Subsets of CD1c+ DCs: Dendritic Cell Versus Monocyte Lineage. Front Immunol. 2020 Sep 30;11:559166. [Content Brief]
[5]. Bourdely P, et al. Transcriptional and Functional Analysis of CD1c+ Human Dendritic Cells Identifies a CD163+ Subset Priming CD8+CD103+ T Cells. Immunity. 2020 Aug 18;53(2):335-352.e8. [Content Brief]