-
Your selected country is
France
- Change country/language
Old Browser
This page has been recently translated and is available in French now.
Looks like you're visiting us from {countryName}.
Would you like to stay on the current country site or be switched to your country?
Expression of IFN-γ by stimulated pig peripheral blood mononuclear cells (PBMC). Pig PBMC were stimulated for 20 hours with PMA (5 ng/ml final concentration, Sigma, Cat. No. P-8139) and ionomycin (500 ng/ml final concentration, Sigma, Cat. No. I-0634) in the presence of BD GolgiStop™ (4 µl/6 ml, Cat. No. 554724.). The PBMC were harvested, fixed, permeabilized, and subsequently stained with 0.015 µg of PE-conjugated mouse anti-porcine IFN-γ antibody (PE-P2G10, Cat. No. 559812) by using the BD Biosciences Pharmingen staining protocol (center panel). To demonstrate specificity of staining, the binding by the PE-P2G10 antibody was blocked by pre-incubation of the fixed/permeabilized cells with unlabeled P2G10 antibody (10 µg; Cat. No. 559961; right panel) prior to staining. The quadrant markers for the bivariate dot plots were set based on the staining profile using 0.12 µg of PE-MOPC-21 isotype control antibody (Cat. No. 554680, left panel) and verified using the unlabeled antibody blocking specificity control.
BD Pharmingen™ PE Mouse Anti-Pig IFN-γ
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Recommended Assay Procedures
IF/Flow: For immunofluorescent staining and flow cytometric analysis, the P2G10 antibody has been found useful to identify and enumerate IFN-γ producing cells within mixed cell populations. PE- conjugated P2G10 antibody (Cat. No. 559812) is especially suitable for these studies. For specific methodology, please visit the online protocols section or chapter on intracellular staining in the Immune Function Handbook, both of which are posted on our web site, www.bdbiosciences.com.
A useful control for demonstrating specificity of staining is either of the following: 1) pre-block the fluorochrome-conjugated P2G10 antibody with ligand prior to staining, or 2) pre-block the fixed/permeabilized cells with unlabeled P2G10 antibody (Cat. No. 559961) prior to staining. The intracellular staining technique and use of blocking controls are described in detail by C. Prussin and D. Metcalfe. A suitable mouse IgG1, κ isotype control for assessing the level of background staining on paraformaldehyde-fixed/saponin-permeabilized porcine cells is PE-MOPC-21 immunoglobulin (Cat. No. 554680); use at comparable concentrations to antibody of interest (eg, ≤ 0.5 µg mAb/1 million cells).
ELISA Capture: The purified P2G10 antibody (Cat. No. 559961) is useful as a capture antibody for a sandwich ELISA for measuring porcine IFN-γ protein levels. Purified P2G10 antibody can be paired with the biotinylated P2C11 antibody (Cat. No. 559958) as the detecting antibody.
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
The P2G10 monoclonal antibody specifically binds to porcine interferon-γ (IFN-γ). The immunogen used to generate the P2G10 hybridoma was recombinant pig IFN-γ protein.
Development References (2)
-
Mateu de Antonio E, Husmann RJ, Hansen R, et al. Quantitative detection of porcine interferon-gamma in response to mitogen, superantigen and recall viral antigen. Vet Immunol Immunopathol. 1998; 61(2-4):265-277. (Immunogen: ELISA). View Reference
-
Prussin C, Metcalfe DD. Detection of intracytoplasmic cytokine using flow cytometry and directly conjugated anti-cytokine antibodies. J Immunol Methods. 1995; 188(1):117-128. (Methodology: IC/FCM Block). View Reference
Please refer to Support Documents for Quality Certificates
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.