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Alexa Fluor® 647 anti-rat IFN-γ Antibody
Alexa Fluor® 647 anti-rat IFN-γ Antibody
507809 25 tests $95.00     
507810 100 tests $225.00     

Product Details

Clone: DB-1
Isotype: Mouse IgG1, κ
Isotype Control:Alexa Fluor® 647 Mouse IgG1, κ Isotype Ctrl (FC)
Reactivity: Mouse, Rat
Immunogen: Recombinant rat IFN-γ
Formulation: Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 0.2% (w/v) BSA (origin USA).
Preparation: The antibody was purified by affinity chromatography, and conjugated with Alexa Fluor® 647 under optimal conditions. The solution is free of unconjugated Alexa Fluor® 647.
Storage & Handling: The antibody solution should be stored undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.
Application:

ICFC - Quality tested

Recommended Usage: Each lot of this antibody is quality control tested by intracellular immunofluorescent staining with flow cytometric analysis. For immunofluorescent staining, the suggested use of this reagent is 5 µl per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.

* Alexa Fluor® 647 has a maximum emission of 668 nm when it is excited at 633nm / 635nm.
** Alexa Fluor® is a registered trademark of Molecular Probes, Inc. Alexa Fluor® dye antibody conjugates are sold under license from Molecular Probes, Inc. for research use only, except for use in combination with microarrays and high content screening, and are covered by pending and issued patents.

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COA:
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Application
Notes:
ELISA Capture1 or ELISPOT Capture2: The purified DB-1 antibody is useful as the capture antibody in a sandwich ELISA or ELISPOT assay, when used in conjunction with the biotinylated poly5109 antibody (Cat. No. 510901) as the detecting antibody and recombinant IFN-γ (Cat. No. 565701) as the standard. The LEAF™ purified antibody is suggested for ELISPOT capture.
Flow Cytometry5: The fluorochrome-labeled DB-1 antibody is useful for intracellular immunofluorescent staining and flow cytometric analysis to identify IFN-γ-producing cells within mixed cell populations. View intracellular cytokine staining protocol
Neutralization3,4: The LEAF™ purified antibody (Endotoxin <0.1 EU/μg, Azide-Free, 0.2 μm sterile-filtered) is recommended for neutralization of rat IFN-γ bioactivity in vivo and in vitro (Cat. No. 507808).
Additional reported applications (for the relevant formats) include: Western blotting1, and immunohistochemistry2 of paraformaldehyde-fixed, saponin-treated frozen tissue sections.
Application
References:
1. Van der Meide P, et al. 1989. Lymphokine Res. 8:439.
2. Nennesmo I, et al. 1989. Brain Res. 504:306.
3. Rayner D, et al. 1987. Scand. J. Immunol. 25:621.
4. Hartung H, et al. 1990. Ann Neurol. 27:247.
5. Bernard I, et al. 1998. Eur. Cytokine Net. 9:613.
PMA+ionomycin-stimulated Lou rat splenocytes (6
PMA+ionomycin-stimulated Lou rat splenocytes (6 hours) stained with DB-1 Alexa Fluor® 647


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Description: Interferon-γ is a potent multifunctional cytokine which is secreted primarily by activated NK cells and T cells. Originally characterized based on anti-viral activities, IFN-γ also exerts anti-proliferative, immunoregulatory, and proinflammatory activities. IFN-γ can upregulate MHC class I and II antigen expression by antigen-presenting cells. The DB-1 antibody reacts with rat and mouse interferon-gamma (IFN-γ). The DB-1 antibody can neutralize the bioactivity of natural or recombinant IFN-γ. The DB-1 antibody has been well characterized for ELISPOT, ELISA, intracellular staining, Western blotting, IHC, and neutralization (in vitro and in vivo).
Other Names: Interferon-γ, Immune interferon, Type II interferon, T cell interferon, Macrophage-activating factor (MAF), IFN-g, IFN-gamma
Structure: Cytokine; dimer; 40-80 kD (Mammalian)
Regulation: Upregulated by IL-2, bFGF, EGF; downregulated by 1-α-25-Dihydroxy vitamin D3, dexamethasone
Cellular Sources: CD8+ and CD4+ T cells, NK cells
Cellular Targets: T cells, B cells, macrophages, NK cells, endothelial cells, fibroblasts
Receptors: IFN-γRα (CDw119) dimerized with IFN-γRβ (AF-1)
Bioactivity/Activities: Antiviral/antiparasitic activities; inhibits proliferation; enhances MHC class I and II expression on APC
Antigen
References:
1. Fitzgerald K, et al. Eds. 2001. The Cytokine FactsBook. Academic Press San Diego.
2. De Maeyer E, et al. 1992. Curr. Opin. Immunol. 4:321.
3. Farrar M, et al. 1993. Annu .Rev. Immunol. 11:571.
4. Gray P, et al. 1987. Lymphokines 13:151.
GeneID: 25712
Latest Publications: View the latest IFN-gamma articles on HighwirePress.com
UniProt: View information about IFN-gamma on UniProt.org
Keywords: Alexa Fluor® 647 anti-rat IFN-γ, DB-1, Alexa Fluor® 647, Interferon-γ, Immune interferon, Type II interferon, T cell interferon, Macrophage-activating factor (MAF), IFN-g, IFN-gamma, Mouse, Rat, Immunology, Antibodies
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DescriptionCloneApplications
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*These products may be covered by one or more Limited Use Label Licenses (see the BioLegend Catalog or our website, www.biolegend.com/terms). BioLegend products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products or to provide a service to third parties without written approval of BioLegend. By use of these products you accept the terms and conditions of all applicable Limited Use Label Licenses. Unless otherwise indicated, these products are for research use only and are not intended for human or animal diagnostic, therapeutic or commercial use.
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Compare Data Across All Formats
This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.

  • FITC anti-rat IFN-γ
    PMA/lonomycin stimulated Lou rat splenocytes

    PMA/lonomycin stimulated Lou rat splenocytes were stained with DB-1 PE.

  • LEAF™ Purified anti-rat IFN-γ
    PMA/lonomycin stimulated Lou rat splenocytes

    PMA/lonomycin stimulated Lou rat splenocytes were stained with DB-1 PE.





  • PE anti-rat IFN-γ
    PMA/lonomycin stimulated Lou rat splenocytes

    PMA/lonomycin stimulated Lou rat splenocytes were stained with DB-1 PE.

  • Purified anti-rat IFN-γ
    PMA/lonomycin stimulated Lou rat splenocytes

    PMA/lonomycin stimulated Lou rat splenocytes were stained with DB-1 PE.





  • Alexa Fluor® 647 anti-rat IFN-γ
    PMA+ionomycin-stimulated Lou rat splenocytes (6

    PMA+ionomycin-stimulated Lou rat splenocytes (6 hours) stained with DB-1 Alexa Fluor® 647

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