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BD PharmingenTM PE Rat Anti-Mouse IL-33R (ST2)
GENERAL CATALOGUE

BD PharmingenTM PE Rat Anti-Mouse IL-33R (ST2)

566311 · 0.1 mg

BDB Bioscience · Cat: 566311

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Catalog No: 566311
Category: reagents
Pack Size: 0.1 mg
Brand: BDB Bioscience

Description

Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multicolor flow cytometric analysis of IL-33R ST2 expression by mouse splenocytes. BALB/c mouse splenic leucocytes were stained with BD Horizon Fixable Viability Stain 510 Cat. No. 564406 followed by staining with Alexa Fluor 488 Rat Anti-Mouse CD4 antibody Cat. No. 557667 and either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; Left Plot or PE Rat Anti-Mouse IL-33R ST2 antibody Cat. No. 566311/566312; Right Plot . The cells were then fixed and permeabilized using the BD Pharmingen Transcription Factor Buffer Set Cat. No. 562574/562725 and stained with Alexa Fluor 647 Rat Anti-Mouse Foxp3 Cat. No. 560401/560402 . Two-color flow cytometric contour plots showing the correlated expression of Foxp3 versus IL-33R ST2 or Ig Isotype control staining were derived from CD4-positive gated events with the forward and side light-scatter characteristics of live cell-discriminated intact lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.

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