Flow cytometric analysis of CXCL9 (MIG) expression in Stimulated mouse peritoneal exudate cells (PEC). Thioglycolate-elicited BALB/c mouse PEC were cultured in complete tissue culture medium with Recombinant Mouse IFN-γ protein (Cat. No. 554587, 10 ng/ml) for 2 hours followed by the addition of lipopolysaccharide (LPS; Sigma, 1 μg/ml). BD GolgiPlug™ Protein Transport Inhibitor (Cat. No. 555029) was then added to both cultures that were further cultured overnight. The cells were harvested, washed, fixed with BD Cytofix™ Fixation Buffer (Cat. No. 554655), and then permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained in BD Perm/Wash™ Buffer with Alexa Fluor® 647 Rat Anti-Mouse CD11b (Cat. No. 557686) and either PE Armenian Hamster IgG1, κ Isotype Control (Cat. No. 553972; Left Plot) or PE Armenian Hamster Anti-Mouse CXCL9 (MIG) antibody (Cat. No. 567163; Left Plot) at 0.25 μg/test. The two-color flow cytometric contour plots showing CXCL9 (MIG) expression (or Ig Isotype control staining) versus CD11b were derived from gated events with the forward and side light-scatter characteristics of intact cells. Flow cytometry and data analysis were performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CXCL9 (MIG) expression in Unstimulated and Stimulated RAW264.7 cells. Cells from the mouse RAW 264.7 (Macrophage; ATCC TIB-71) cell line were cultured in complete tissue culture medium without activators [Unstimulated Cells] or with Recombinant Mouse IFN-γ protein (Cat. No. 554587, 10 ng/ml) for 2 hours followed by the addition of lipopolysaccharide (LPS; Sigma, 1 μg/ml) [Stimulated Cells]. BD GolgiPlug™ Protein Transport Inhibitor (Cat. No. 555029) was then added to both cultures that were further cultured overnight. The cells were harvested, washed, fixed with BD Cytofix™ Fixation Buffer (Cat. No. 554655), and then permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained in BD Perm/Wash™ Buffer with PE Armenian Hamster IgG1, κ Isotype Control (Cat. No. 553972; dashed line histogram) or PE Armenian Hamster Anti-CXCL9 (MIG) antibody (Cat. No. 567163; solid and dotted line histograms) at 0.25 μg/test. Left Plot: The fluorescence histogram showing CXCL9 (MIG) expression (solid line) or Ig Isotype control staining (dashed line) were derived from gated events with the light-scatter characteristics of intact cells. Right Plot: The histograms showing CXCL9 (MIG) expression in Unstimulated Cells (dotted line) versus Stimulated Cells (solid line) were overlaid for the sake of direct comparison as shown. Flow cytometry and data analysis were performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
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Flow cytometric analysis of CXCL9 (MIG) expression in Stimulated mouse peritoneal exudate cells (PEC). Thioglycolate-elicited BALB/c mouse PEC were cultured in complete tissue culture medium with Recombinant Mouse IFN-γ protein (Cat. No. 554587, 10 ng/ml) for 2 hours followed by the addition of lipopolysaccharide (LPS; Sigma, 1 μg/ml). BD GolgiPlug™ Protein Transport Inhibitor (Cat. No. 555029) was then added to both cultures that were further cultured overnight. The cells were harvested, washed, fixed with BD Cytofix™ Fixation Buffer (Cat. No. 554655), and then permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained in BD Perm/Wash™ Buffer with Alexa Fluor® 647 Rat Anti-Mouse CD11b (Cat. No. 557686) and either PE Armenian Hamster IgG1, κ Isotype Control (Cat. No. 553972; Left Plot) or PE Armenian Hamster Anti-Mouse CXCL9 (MIG) antibody (Cat. No. 567163; Left Plot) at 0.25 μg/test. The two-color flow cytometric contour plots showing CXCL9 (MIG) expression (or Ig Isotype control staining) versus CD11b were derived from gated events with the forward and side light-scatter characteristics of intact cells. Flow cytometry and data analysis were performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CXCL9 (MIG) expression in Unstimulated and Stimulated RAW264.7 cells. Cells from the mouse RAW 264.7 (Macrophage; ATCC TIB-71) cell line were cultured in complete tissue culture medium without activators [Unstimulated Cells] or with Recombinant Mouse IFN-γ protein (Cat. No. 554587, 10 ng/ml) for 2 hours followed by the addition of lipopolysaccharide (LPS; Sigma, 1 μg/ml) [Stimulated Cells]. BD GolgiPlug™ Protein Transport Inhibitor (Cat. No. 555029) was then added to both cultures that were further cultured overnight. The cells were harvested, washed, fixed with BD Cytofix™ Fixation Buffer (Cat. No. 554655), and then permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained in BD Perm/Wash™ Buffer with PE Armenian Hamster IgG1, κ Isotype Control (Cat. No. 553972; dashed line histogram) or PE Armenian Hamster Anti-CXCL9 (MIG) antibody (Cat. No. 567163; solid and dotted line histograms) at 0.25 μg/test. Left Plot: The fluorescence histogram showing CXCL9 (MIG) expression (solid line) or Ig Isotype control staining (dashed line) were derived from gated events with the light-scatter characteristics of intact cells. Right Plot: The histograms showing CXCL9 (MIG) expression in Unstimulated Cells (dotted line) versus Stimulated Cells (solid line) were overlaid for the sake of direct comparison as shown. Flow cytometry and data analysis were performed using a BD LSRFortessa™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
製品詳細
BD Pharmingen™
Cxcl9; Mig; CMK; M119; crg-10; Scyb9
Mouse (QC Testing)
Armenian Hamster IgG, κ
Mouse CXCL9 Recombinant Protein
Intracellular staining (flow cytometry) (Routinely Tested)
0.2 mg/ml
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO
Preparation and Storage
Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated with R-PE under optimum conditions, and unconjugated antibody and free PE were removed.
推奨アッセイ手順
BD™ CompBeads can be used as surrogates to assess fluorescence spillover (Compensation). When fluorochrome conjugated antibodies are bound to CompBeads, they have spectral properties very similar to cells. However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls. It is strongly recommended that when using a reagent for the first time, users compare the spillover on cell and CompBead to ensure that BD Comp beads are appropriate for your specific cellular application.
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- An isotype control should be used at the same concentration as the antibody of interest.
- 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.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
- Although hamster immunoglobulin isotypes have not been well defined, BD Biosciences Pharmingen has grouped Armenian and Syrian hamster IgG monoclonal antibodies according to their reactivity with a panel of mouse anti-hamster IgG mAbs. A table of the hamster IgG groups, Reactivity of Mouse Anti-Hamster Ig mAbs, may be viewed at http://www.bdbiosciences.com/documents/hamster_chart_11x17.pdf.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
関連製品
Stain Buffer (FBS) RUO
サイズ
500 mL
カタログ番号
554656
Stain Buffer (BSA) RUO
サイズ
500 mL
カタログ番号
554657
Fixation Buffer RUO
サイズ
100 mL
カタログ番号
554655
Perm/Wash Buffer RUO
サイズ
100 mL
カタログ番号
554723
PE Hamster IgG1 κ Isotype Control RUO
サイズ
0.1 mg
カタログ番号
553972
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Alexa Fluor® 647 Rat Anti-CD11b RUO
サイズ
0.1 mg
カタログ番号
557686
567163 Rev. 1
抗体の詳細
MIG-2F5.5
The MIG 2F5.5 monoclonal antibody specifically recognizes MIG (Monokine induced by gamma interferon) which is also known as C-X-C motif chemokine 9 (CXCL9) or Small-inducible cytokine B9 (Scyb9). Mouse CXCL9 (MIG) is encoded by Cxcl9 and belongs to the C-X-C family of chemokines. CXCL9 (MIG) production is induced in a variety of cells including macrophages, hepatocytes, and endothelial cells in response to gamma interferon (IFN-γ). The seven-transmembrane G-protein coupled receptor termed CXCR3, also known as CD183, serves as the cell surface signaling receptor for CXCL9 (MIG). This chemotactic factor attracts activated and memory CD4+ and CD8+ T cells including Type-1 (Th1-like) CD4+ T cells as well as natural killer (NK) cells. CXCL9 (MIG) plays important roles in promoting protective immunity through the attraction of CXCR3+ T cells and NK cells but can also function in inflammation and autoimmune diseases.
567163 Rev. 1
フォーマットの詳細
PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
567163 Rev.1
引用＆参考文献
Development References (4)
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Asai A, Tsuda Y, Kobayashi M, Hanafusa T, Herndon DN, Suzuki F. Pathogenic role of macrophages in intradermal infection of methicillin-resistant Staphylococcus aureus in thermally injured mice.. Infect Immun. 2010; 78(10):4311-9. (Clone-specific: Flow cytometry). View Reference
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Krug A, Uppaluri R, Facchetti F, et al. IFN-producing cells respond to CXCR3 ligands in the presence of CXCL12 and secrete inflammatory chemokines upon activation. J Immunol. 2002; 169(11):6079-6083. (Immunogen: ELISA). View Reference
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Marcus AJ, Ullman HL, Safier LB. Lipid composition of subcellular particles of human blood platelets.. J Lipid Res. 1969; 10(1):108-14. (Biology). View Reference
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Sung JH, Zhang H, Moseman EA, et al. Chemokine guidance of central memory T cells is critical for antiviral recall responses in lymph nodes.. Cell. 2012; 150(6):1249-63. (Clone-specific: Flow cytometry, Immunofluorescence). View Reference
567163 Rev. 1
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.
