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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 RA3-6B2 monoclonal antibody reacts with exon A-restricted isoform of mouse CD45, a 220 kDa surface molecule. CD45R/B220 epitope is mainly expressed by the B cell lineage from early Pro-B to mature B cells. However, some activated T cells, lymphokine activated killer cells (LAK), NK cell progenitors in the bone marrow, and T cells of the lpr/lpr mutant mouse also express this antigen. Applications ReportedFor research use only, not for diagnostic or therapeutic use. This RA3-6B2 antibody has been reported for use in flow cytometric analysis. Applications TestedThis RA3-6B2 antibody has been pre-titrated and tested by flow cytometric analysis of mouse splenocytes 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 605NCrat IgG2b (cat. 93-4321) should be used at 5 μl/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
Morse, H. C. d., W. F. Davidson, et al. 1982. Abnormalities induced by the mutant gene Ipr: expansion of a unique lymphocyte subset. J Immunol. 129(6): 2612-5. Coffman, R. L. 1982. Surface antigen expression and immunoglobulin gene rearrangement during mouse pre-B cell development. Immunol Rev. 69: 5-23. Schuhmann B, Dietrich A, et al. 2005. A role for brain-derived neurotrophic factor in B cell development. J Neuroimmunol. 163(1-2):15-23. (IHC frozen, PubMed) Monteith CE, Chelack BJ, et al. 1996. Identification of monoclonal antibodies for immunohistochemical staining of feline B lymphocytes in frozen and formalin-fixed paraffin-embedded tissues. Can J Vet Res. 60(3):193-8. (IHC frozen and paraffin, PubMed) Related ProductsCat. 00-3222 eFluor™ NC Flow Cytometry Staining Buffer Cat. 93-4321 eFluor™ 605NC Rat IgG2a Isotype Control |
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