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eFluor products are not offered for sale or use in certain regions. Please contact an eBioscience representative for more information on whether our products are available for purchase in your area. Questions? Please consult our answers to frequently asked questions at http://www.ebioscience.com/faq. DescriptionThe LN3 mAb reacts with the human major histocompatibility complex (MHC) class II, HLA-DR. HLA-DR is expressed on the surface of human antigen presenting cells (APC) including B cells, monocytes, macrophages, DCs, and activated T cells. HLA-DR is a heterodimeric transmembrane protein composed of α and β subunits and plays an important role in the presentation of peptides to CD4+ T lymphocytes. Applications ReportedFor research use only, not for diagnostic or therapeutic use. This LN3 antibody has been reported for use in flow cytometric analysis. Applications TestedThis LN3 antibody has been pre-titrated and tested by flow cytometric analysis of normal human peripheral blood cells using eFluorTM NC Flow Cytometry Staining Buffer (cat. 00-3222). This can be used at 5 μl/test (one million cells in a 100μL total staining volume). The isotype control eFluorTM 605NC mouse IgG2b (cat. 93-4732) should be used at 5μL/test. Laser/Filter Recommendation: When using eFluorTM 605NC, we recommend excitation with the 405nm violet laser with an appropriate filter set, such as the 595LP dichroic mirror with the 605/40 bandpass filter. An acceptable alternative is the 610/20 bandpass filter. Please contact eBioscience Technical Support for more information. Buffer Recommendation: Comparison of eFluorTM Nanocrystal conjugated antibody staining in different buffers has demonstrated that optimal performance is seen with the eFluorTM NC Flow Cytometry Staining Buffer (cat. 00-3222). For a limited time the eFluorTM NC Flow Cytometry Staining Buffer will be provided complimentary with the purchase of eFluorTM Nanocrystal conjugated products. For a comparison of staining with different buffers, click here. Whole Blood Recommendation: If staining whole blood samples, collection into heparin or sodium citrate-containing tubes is recommended. If EDTA is being used as an anti-coagulant, lysis of RBCs with eBioscience 1X RBC Lysis Buffer (cat. 00-4333) before staining is required. Click here to view our list of eFluorTM Nanocrystal Frequently Asked Questions. References
Fullen, D. R. and J. T. Headington (1998). "Factor XIIIa-positive dermal dendritic cells and HLA-DR expression in radial versus vertical growth-phase melanomas [see comments]." J Cutan Pathol 25(10): 553-8. Hua, Z. X., K. E. Tanaka, et al. (1998). "Immunoreactivity for LN2 and LN3 distinguishes small cell carcinomas from non-small cell carcinomas in the lung." Hum Pathol 29(12): 1441-6. Ioachim, H. L., S. E. Pambuccian, et al. (1996). "Lymphoid monoclonal antibodies reactive with lung tumors. Diagnostic applications." Am J Surg Pathol 20(1): 64-71. Davey, F. R., S. Olson, et al. (1988). "The immunophenotyping of extramedullary myeloid cell tumors in paraffin-embedded tissue sections." Am J Surg Pathol 12(9): 699-707. Norton, A. J. and P. G. Isaacson (1987). "Detailed phenotypic analysis of B-cell lymphoma using a panel of antibodies reactive in routinely fixed wax-embedded tissue." Am J Pathol 128(2): 225-40. Related ProductsCat. 00-3222 eFluor™ NC Flow Cytometry Staining Buffer |
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