Cell Signaling Technology

Product Pathways - Flow Cytometry

DC-SIGN (D7F5C) XP® Rabbit mAb (PE Conjugate) #71481

Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
F 1:50 Human, Endogenous Rabbit IgG

Species cross-reactivity is determined by western blot.

Applications Key: F=Flow Cytometry,

Specificity / Sensitivity

DC-SIGN (D7F5C) XP® Rabbit mAb (PE Conjugate) recognizes endogenous levels of total DC-SIGN protein. This antibody does not cross-react with DC-SIGNR.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human DC-SIGN protein.


This Cell Signaling Technology antibody is conjugated to phycoerythrin (PE) and tested in-house for direct flow cytometry analysis in human cells. This antibody is expected to exhibit the same species cross-reactivity as the unconjugated DC-SIGN (D7F5C) XP® Rabbit mAb #13193.

Flow Cytometry

Flow Cytometry

Flow cytometric analysis of MUTZ-3 cells, undifferentiated (blue) or differentiated (green) into immature dendritic-like cells by treatment with Human Granulocyte Macrophage Colony Stimulating Factor (hGM-CSF) #8922 (100 ng/ml), Human Tumor Necrosis Factor-α (hTNF-α) #8902 (2.5 ng/ml) and Human Interleukin-4 (hIL-4) #8919 (100 ng/ml) for 10 days, using DC-SIGN (D7F5C) XP® Rabbit mAb (PE Conjugate).

Flow Cytometry

Flow Cytometry

Flow cytometric analysis of THP-1 cells, undifferentiated (blue) or differentiated (green) by treatment with TPA (12-O-Tetradecanoylphorbol-13-Acetate) #4174 (80 nM) overnight and Human Interleukin-4 (hIL-4) #8919 (100 ng/ml) for 48 hours after TPA, using DC-SIGN (D7F5C) XP® Rabbit mAb (PE Conjugate) (solid lines) and a concentration matched isotype control Rabbit (DA1E) mAb IgG XP® Isotype Control (PE Conjugate) #5742 (dashed lines).


DC-SIGN (CD209, CLEC4L) is a C-type lectin receptor expressed by dendritic cells (DCs) (1,2). The DC-SIGN transcript can undergo several splicing events to generate at least thirteen different transmembrane and soluble isoforms (3). DC-SIGN responds to a broad range of pathogens due to its ability to recognize both mannose and fructose carbohydrates, and is well studied for its role in HIV infection. Recognition of the HIV envelope glycoprotein gp120 by DC-SIGN leads to internalization of HIV by DCs and facilitates transmission of the virus to CD4+ T cells (2,4). DC-SIGN also mediates adhesion to T cells through interaction with ICAM-3, as well as transmigration across the endothelium by binding to ICAM-2 (1,5). The DC-SIGN receptor can modulate TLR signaling by activating the kinase Raf-1 (6,7). The closely related molecule DC-SIGNR (L-SIGN, CLEC4M) is 77% homologous to DC-SIGN and likely arose through a gene duplication event (8). Like DC-SIGN, DC-SIGNR binds mannose carbohydrates on the surface of pathogens (8,9). However, the expression patterns of the two receptors differ, as DC-SIGNR expression is restricted to endothelial cells of the liver, lymph node, and placenta (10). Murine cells contain a set of related molecules, SIGNR1-SIGNR8 (11). Based on sequence analysis, there is no clear murine ortholog to human DC-SIGN, however SIGNR3 is the most functionally similar due to its ability to recognize both mannose and fructose structures (11).

  1. Geijtenbeek, T.B. et al. (2000) Cell 100, 575-85.
  2. Geijtenbeek, T.B. et al. (2000) Cell 100, 587-97.
  3. Mummidi, S. et al. (2001) J Biol Chem 276, 33196-212.
  4. Kwon, D.S. et al. (2002) Immunity 16, 135-44.
  5. Geijtenbeek, T.B. et al. (2000) Nat Immunol 1, 353-7.
  6. Gringhuis, S.I. et al. (2007) Immunity 26, 605-16.
  7. Gringhuis, S.I. et al. (2010) Nat Immunol 11, 419-26.
  8. Bashirova, A.A. et al. (2001) J Exp Med 193, 671-8.
  9. Mitchell, D.A. et al. (2001) J Biol Chem 276, 28939-45.
  10. Pöhlmann, S. et al. (2001) Proc Natl Acad Sci U S A 98, 2670-5.
  11. Powlesland, A.S. et al. (2006) J Biol Chem 281, 20440-9.

Application References

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Companion Products

For Research Use Only. Not For Use In Diagnostic Procedures.

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

XP is a registered trademark of Cell Signaling Technology, Inc.

Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.

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