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CD303 (BDCA-2)
Description
Clone AC144 recognizes the the CD303 (BDCA-2) antigen1,3 which is expressed on human plasmacytoid dendritic cells in blood, lymphoid (e.g. tonsils and bone marrow) and non-lymphoid tissue.3,6 Specific expression allows direct identification of plasmacytoid dendritic cells using just one marker.1–11 CD303 (BDCA-2)+ plasmacytoid dendritic cells in blood and bone marrow are CD11c–, CD123high, CD4+, Lin–, CD45RA+, CD304 (BDCA-4/Neuropilin-1)+, CD141 (BDCA-3)low, CD1c (BDCA-1)–, CD14–, and CD2–. They express neither myeloid lineage markers (CD13, CD33) nor Fc receptors (CD32, CD64, FcRI).1,6 CD303 (BDCA-2) is strongly expressed on freshly isolated plasmacytoid dendritic cells but down-regulated within 48 hours of culturing.1 Unlike CD304 (BDCA-4/Neuropilin-1), CD303 (BDCA-2) is not detectable on ex vivo generated monocyte-derived or hematopoietic precursor cell-derived CD1a+ dendritic cells.1,9
The CD303 (BDCA-2) antigen is a novel type II transmembrane C-type lectin.3 Remarkably, plasmacytoid dendritic cells can take up ligands via CD303 (BDCA-2), then process and present the ligands to T cells.1,3 Unlike binding of antibodies to CD304 (BDCA-4), binding of antibodies to CD303 (BDCA-2) inhibits type I IFN production, which is induced in plasmacytoid dendritic cells by, for example, the influenza virus.3,6
Applications
Direct identification of CD303 (BDCA-2)+ plasmacytoid dendritic cells in blood, lymphoid and non-lymphoid tissue by immunofluorescent (or immuno­cytochemical) staining and flow cytometric analysis.1,3, 5–11 The antibody is suitable for staining of fresh or formaldehyde-fixed cells in suspension and for staining of, for example, air-dried, acetone-fixed cryosections.3,5 Staining with CD303 (BDCA-2) antibodies is recommended for flow cytometric evaluation if plasmacytoid dendritic cells are isolated using the CD304 CD304 (BDCA-4/Neuropilin-1) MicroBead Kit.3
CD303 (BDCA-2) antibodies have been used, for example, to identify, characterize, and enumerate plasmacytoid dendritic cells in whole blood of healthy and HIV-infected individuals, and for analyzing the role of DC-SIGN in HIV infection and transmission.7,11 Furthermore, CD303 (BDCA-2) antibodies were used to identify and enumerate plasmacytoid dendritic cells in blood and bone marrow samples before and after hematopoietic stem cell mobilization8 or transplantation10. CD303 (BDCA-2) antibodies were also used for immunohistochemical staining, for example to identify plasmacytoid dendritic cells in tissue sections from patients with different inflammatory skin diseases.5,12,13
CloneIsotype
AC144Mouse IgG1
 
Figure 1
Human PBMCs were stained with CD303 (BDCA-2), lineage marker (CD3, CD16, CD14, CD19, CD20, CD56), CD123, and CD11c antibodies. Flow cytometric analysis confirms that CD303 (BDCA-2)+ plasmacytoid dendritic cells are Lin–, CD123+ and CD11c–, and that CD303 (BDCA-2) is exclusively expressed on plasmacytoid dendritic cells.
Figure 2
Direct identification of plasmacytoid dendritic cells in cryosections of tonsils by immunofluorescent staining. Sections were stained with CD303 (BDCA-2)-FITC (green) and non-conjugated monoclonal antibody against CD123 (A), CD20 (B), CD8 (C) or HLA-DR (D), respectively. Staining with non-conjugated monoclonal antibodies was revealed by secondary staining with biotinylated anti-isotype antibodies and Texas red-conjugated streptavidin (red).
A
B
C
D
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Products
CD303 (BDCA-2)-FITC, human
for 100 tests (1)
Download data sheet
130-090-510
Qty:
 

CD303 (BDCA-2)-PE, human
for 100 tests (1)
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130-090-511
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CD303 (BDCA-2)-APC, human
for 100 tests (1)
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130-090-905
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CD303 (BDCA-2)-Biotin, human
for 100 tests (2)
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130-090-691
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CD303 (BDCA-2) pure, human
100 ÎĽg in 1 mL
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130-090-690
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(1) One test corresponds to fluorescent labeling of up to 107 cells in a total volume of 100 ÎĽL.
(2) One test corresponds to labeling of up to 107 cells in a total volume of 100 ÎĽL.
Related products
CD304 (BDCA-4/Neuropilin-1) MicroBead Kit, human (#130-090-532)
Mouse IgG1 - isotype control Antibodies
MACS References
1. Dzionek et al. (2000) J. Immunol. 165: 6037–6046.[898]
2. Grabbe et al. (2000) Immunol. Today 21: 431–433.[899]
3. Dzionek et al. (2001) J. Exp. Med. 194: 1823–1834.[1264]
4. Rönnblom and Alm (2001) J. Exp. Med. 194: F59–F63.[1265]
5. Wollenberg et al. (2002) Invest. Dermatol. 119: 1096–1102.[2674]
6. Dzionek et al. (2002) Human Immunol. 36: 1133–1148.[2423]
7. Chehimi et al. (2002) J. Immunol. 168: 4769–4801.[2301]
8. Arpinati et al. (2002) Bone Marrow Transplant. 29: 887–891.[2237]
9. Ebner et al. (2002) J. Immunol. 168: 6199–6207.[2200]
10. Clark et al. (2003) Transplant. 75: 221–225.[2873]
11. De Wit et al. (2004) Blood 103: 1030–1032.[4224]
12. Nestle et al. (2005) J. Exp. Med. 202: 135–143.[7359]
13. Ebner et al. (2004) Int. Immunol. 16: 877–887.[8583]
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