Flow cytometric analysis of Jurkat cells using β-Actin (8H10D10) Mouse mAb #3700 detected with Anti-mouse IgG (H+L), F(ab')2 Fragment (PE Conjugate) (solid line) compared to concentration matched Mouse (G3A1) mAb IgG1 Isotype Control #5415 (dashed line).Learn more about how we get our images.
The optimal dilution of the anti-species antibody should be determined for each primary antibody by titration. However, a final dilution of 1:250 - 1:1000 should yield acceptable results for flow cytometry assays.
Supplied in PBS (pH 7.2), less than 0.1% sodium azide and 2 mg/ml BSA. Store at 4°C. Do not aliquot the antibody. Protect from light. Do not freeze.
Anti-mouse IgG (H+L), F(ab')2 Fragment was conjugated to phycoerythrin (PE) under optimal conditions. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
F(ab')2 fragments are prepared from goat antibodies that have been affinity purified and shown no reactivity against non-immunoglobulin mouse serum proteins or bovine, goat, human, rabbit or rat IgG based on immunoelectrophoresis (IEP) testing.
This product has been optimized for use as a secondary antibody in flow cytometry. Fluorescent anti-species IgG conjugates are ideal for flow cytometry and immunofluorescence. Cell Signaling Technology’s strict quality control procedures assure that each conjugate provides optimal specificity and fluorescence.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
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