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BD Pharmingen™ Purified Rat Anti-Mouse Follicular Dendritic Cell
Clone FDC-M1




Immunohistochemistry of follicular dendritic cells. Frozen sections of mouse spleen was reacted with the FDC-M1 antibody. Follicular dendritic cells can be identified by the intense brown labeling of their cell membranes. Magnification 20X.


BD Pharmingen™ Purified Rat Anti-Mouse Follicular Dendritic Cell

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Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Recommended Assay Procedures
Immunohistochemistry: The FDC-M1 clone reactive against mouse follicular dendritic cells is tested for immunohistochemical staining of acetone-fixed frozen sections. Tissues tested were mouse spleen, thymus and small intestine. The antibody stains follicular dendritic cells and their processes. For optimal indirect immunohistochemical staining, the FDC-M1 antibody should be titrated (1-10 to 1-50 dilution) and visualized via a three-step staining procedure in combination with polyclonal, biotin conjugated anti-rat Igs (multiple adsorbed) (Cat. No. 559286) as the secondary antibody and treptravidin-HRP (Cat. No. 550946) together with the DAB detection system (Cat. No. 550880). More conveniently, the anti-rat Ig HRP detection kit (Cat. No. 551013) that provides the biotinylated secondary antibody, antibody diluent and the detection system can be used to stain for anti-mouse follicular dendritic cells. Adetailed protocol of the immunohistochemical procedure is enclosed. The clone FDC-M1 is not recommended for formalin-fixed paraffin embedded sections.
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
- Source of all serum proteins is from USDA inspected abattoirs located in the United States.
Follicular Dendritic Cells (FDC) form a structural network within the lymphoid follicles and are involved in antigen presentation to B cells for generating an immune response and for the maintenance of immunological memory. FDCs are believed to provide signals to B cells to induce their proliferation. In LCMV mediated immunosuppression there is evidence of T-cell dependent destruction of macrophages and follicular dendritic cells. The FDC-M1 antibody recognizes follicular dendritic cells and their dendritic processes.
Development References (3)
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Gray D, Kosco M, Stockinger B. Novel pathways of antigen presentation for the maintenance of memory. Int Immunol. 1991; 3(2):141-148. (Biology: Immunohistochemistry-formalin (antigen retrieval required), Immunohistochemistry-frozen). View Reference
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Kosco, Pflugfelder, and Gray. Follicular dendritic cell-dependent adhesion and proliferation of B cells in vitro. . J Immunol. 1992; 148:2331-2339. (Biology: Immunohistochemistry-formalin (antigen retrieval required), Immunohistochemistry-frozen). View Reference
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Odermatt B, Eppler M, Leist TP, Hengartner H, Zinkernagel RM. Virus-triggered acquired immunodeficiency by cytotoxic T-cell-dependent destruction of antigen-presenting cells and lymph follicle structure. Proc Natl Acad Sci U S A. 1991; 88(18):8252-8256. (Biology: Immunohistochemistry-formalin (antigen retrieval required), Immunohistochemistry-frozen). View Reference
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
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