Product Information
Contents: eFluorTM 605NC anti-mouse/human CD45R ( B220)
Catalog Number: 93-0452
Sizes: 25 tests, 100 tests
Formulation: aqueous buffer, 0.09% sodium azide, contains stabilizer if necessary
Storage Conditions: Store at 4°C. DO NOT FREEZE. LIGHT-SENSITIVE MATERIAL.
Clone: RA3-6B2
Isotype: Rat IgG2a, κ
HLDA No.: N/A
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Staining of BALB/c splenocytes with APC anti-mouse CD3e (145-2C11) (cat. 17-0031) and eFluor™ 605NC Rat IgG2a Isotype Control (cat. 93-4321) (left) or eFluor™ 605NC anti-mo/hu CD45R (B220) (RA3-6B2) (right). Total viable cells were used for analysis.
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Questions? Please consult our answers to frequently asked questions at
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Description
The 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 Reported
For research use only, not for diagnostic or therapeutic use. This RA3-6B2 antibody has been reported for use in flow cytometric analysis.
Applications Tested
This RA3-6B2 antibody has been pre-titrated and tested by flow cytometric analysis of mouse splenocytes using eFluor
TM 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 eFluor
TM 605
NCrat IgG2b (cat.
93-4321) should be used at 5 μl/test.
Laser/Filter Recommendation: When using eFluor
TM 605
NC, 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 eFluor
TM Nanocrystal conjugated antibody staining in different buffers has demonstrated that optimal performance is seen with the eFluor
TM NC Flow Cytometry Staining Buffer (cat.
00-3222). 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 Products
Cat. 00-3222 eFluor™ NC Flow Cytometry Staining BufferCat. 93-4321 eFluor™ 605NC Rat IgG2a Isotype Control