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| Overview |
| The CD205 antibodies can be used for the detection or subset specific analysis of mouse dendritic cells in combination with other markers, such as CD11c, CD8, or MHC Class II. They are suitable for the identification and enumeration of CD205+ cells by flow cytometry or fluorescence microscopy. |
| Details |
Background information The CD205 antibody recognizes a 205 kDa integral membrane glycoprotein also known as DEC205 (dendritic and epithelial cells, 205 kDa).1,2 This membrane protein acts as an endocytic receptor and thereby mediates efficient processing and presentation of antigens in vivo, leading to the induction of T cell immunity or tolerance3. CD205 is expressed at high levels on mouse dendritic cells (DCs) in the skin (Langerhans cells), on DCs residing in the T cell areas of peripheral lymphoid organs, and on DCs generated in vitro from bone marrow progenitors.4 To a much lower extent, CD205 is also expressed on mature B cells, granulocytes, and T cells.1,2 |
| Clone | Isotype |
| NLDC-145 | Rat IgG2a |
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| Figure 1 |
| Mouse spleen cells were stained with CD8-conjugated antibodies as well as with CD205 (DEC205) antibodies conjugated to PE (A), APC (B), or Biotin (C). Cells stained with CD205 (DEC205)-Biotin were stained with Anti-Biotin-PE in addition. Samples were then analyzed by flow cytometry. Cell debris and dead cells were excluded from the analysis based on scatter signals and PI fluorescence. |
| A |
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| B |
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| C |
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| Products |
| CD205 (DEC205)-PE, mouse |
- for 100 tests (1) Download datasheet 130-092-286
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| CD205 (DEC205)-APC, mouse |
- for 100 tests (1) Download datasheet 130-092-285
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| CD205 (DEC205)-Biotin, mouse |
- for 100 tests (2) Download datasheet 130-092-468
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| (1) One test corresponds to fluorescent labeling of up to 107 cells in a total volume of 100 μL. |
| (2) One test corresponds to labeling of up to 107 cells in a total volume of 100 μL. |
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| References |
| 1. Inaba et al. (1995) Cell. Immun. 163: 148–156. |
| 2. Witmer-Pack et al. (1995) Cell. Immun. 163: 157–162. |
| 3. Bonifaz et al. (2002) J. Exp. Med. 196: 1627–1638. |
| 4. Kraal et al. (1986) J. Exp. Med. 163: 981–997. |
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