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ELISA Detection: The R4-6A2 antibody has been found to be useful in sandwich ELISAs that measure mouse IFN-γ protein levels. The Biotin Anti-Mouse IFN-γ antibody (Cat. No. 551506) can be used as a detection antibody along with Purified Rat Anti-Mouse IFN-γ (Cat. No. 551309) as the capture antibody and Recombinant Mouse IFN-γ (Cat. No. 554587) as the standard. The Biotin Anti-Mouse IFN-γ antibody should be titrated 0.5 -2 µg/ml to determine its optimal concentration for ELISA detection. To obtain linear standard curves, doubling dilutions of mouse IFN-γ ranging from ~500 to 5 pg/ml are recommended for inclusion in each ELISA plate. For specific methodology, please visit our website, http://www.bdbiosciences.com/us/s/resources, and go to the protocols section under "ELISA and ELISPOT." For maximal sensitivity, an overnight incubation (4°C) of samples/standards with the coated capture antibody is suggested. Note: This ELISA pair is recommended primarily for measuring cytokine from experimental cell culture systems. These ELISA reagents are not recommended for assaying serum or plasma samples. For measuring mouse IFN-γ in serum or plasma our Mouse IFN-γ (AN-18) ELISA Set (Cat. No. 551866) or Mouse IFN-γ ELISA Kit II (Cat. No. 558258) are specially formulated and recommended.
The R4-6A2 antibody reacts with mouse interferon-γ (IFN-γ). The immunogen used to generate the R4-6A2 hybridoma was partially purified mouse IFN-γ protein. This is a neutralizing antibody.
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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.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product 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.