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Two-color flow cytometric analysis of PLZF expression in human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were subsequently washed with BD Perm/Wash™ Buffer (Cat. No. 554723) and stained with Alexa Fluor® 647 Mouse Anti-Human NCAM-1 (CD56) antibody (Cat. No. 563443) and either BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat. No. 562292; Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Cat. No. 565738; Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD56 versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
Two-color flow cytometric analysis of PLZF expression in mouse thymocytes. BALB/c mouse thymocytes were stained with APC Hamster Anti-Mouse CD3e antibody (Cat. No. 553066/561826). The cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution The cells were then washed with BD Perm/Wash™ Buffer and stained with either BD Horizon PE-CF594 Mouse IgG1, κ Isotype Control (Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD3e versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light- scatter characteristics of intact thymocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
Two-color flow cytometric analysis of PLZF expression in human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were subsequently washed with BD Perm/Wash™ Buffer (Cat. No. 554723) and stained with Alexa Fluor® 647 Mouse Anti-Human NCAM-1 (CD56) antibody (Cat. No. 563443) and either BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat. No. 562292; Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Cat. No. 565738; Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD56 versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
Two-color flow cytometric analysis of PLZF expression in mouse thymocytes. BALB/c mouse thymocytes were stained with APC Hamster Anti-Mouse CD3e antibody (Cat. No. 553066/561826). The cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution The cells were then washed with BD Perm/Wash™ Buffer and stained with either BD Horizon PE-CF594 Mouse IgG1, κ Isotype Control (Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD3e versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light- scatter characteristics of intact thymocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
Two-color flow cytometric analysis of PLZF expression in human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were subsequently washed with BD Perm/Wash™ Buffer (Cat. No. 554723) and stained with Alexa Fluor® 647 Mouse Anti-Human NCAM-1 (CD56) antibody (Cat. No. 563443) and either BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat. No. 562292; Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Cat. No. 565738; Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD56 versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
Two-color flow cytometric analysis of PLZF expression in mouse thymocytes. BALB/c mouse thymocytes were stained with APC Hamster Anti-Mouse CD3e antibody (Cat. No. 553066/561826). The cells were fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution The cells were then washed with BD Perm/Wash™ Buffer and stained with either BD Horizon PE-CF594 Mouse IgG1, κ Isotype Control (Left Plot) or BD Horizon PE-CF594 Mouse Anti-PLZF antibody (Right Plot). The two-color flow cytometric contour plots showing the correlated expression of CD3e versus PLZF (or Ig Isotype control staining) were derived from gated events with the forward and side light- scatter characteristics of intact thymocytes. Flow cytometric analyses were performed using a BD LSRFortessa™ Cell Analyzer System.
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The R17-809 monoclonal antibody recognizes promyelocytic leukemia zinc finger protein (PLZF). PLZF is also known as zinc finger and BTB domain containing 16 (ZBTB16) and Zinc finger protein 145. PLZF is a member of the BTB/POZ-ZF family of transcription factors that includes Th-POK (Zbtb7b) which is involved in CD4+ T cell fate determination. PLZF serves multiple functions. In the immune system, PLZF is involved in the developmental regulation of innate immune lymphocytes including NKT cells, a subset of γδ T cells, and mucosal associated invariant T (MAIT) cells. The R17-809 hybridoma was generated from a mouse immunized with recombinant mouse PLZF protein. The R17-809 antibody crossreacts with both mouse and human PLZF.
This antibody is conjugated to BD Horizon PE-CF594, which has been developed exclusively by BD Biosciences as a better alternative to PE-Texas Red®. PE-CF594 excites and emits at similar wavelengths to PE-Texas Red® yet exhibits improved brightness and spectral characteristics. Due to PE having maximal absorption peaks at 496 nm and 564 nm, PE-CF594 can be excited by the blue (488-nm), green (532-nm) and yellow-green (561-nm) lasers and can be detected with the same filter set as PE-Texas Red® (eg 610/20-nm filter).
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.