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BD PharmingenTM PE Mouse Anti-Human CD11c

566730 ·

BDB Bioscience · Cat: 566730

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Catalog No: 566730
Category: reagents
Brand: BDB Bioscience

Description

Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific. Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific. Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific. Show More Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific. Show More Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific. Two-parameter flow cytometric analysis of CD11c expression on human peripheral blood leucocyte populations. Human peripheral blood collected with heparin as the preferred anticoagulant rather than EDTA was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 557714; Left Panel or PE Mouse Anti-Human CD11c antibody Cat. No. 566730; Right Panel at 0.5 mug. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter pseudocolor density plots showing the correlated expression of CD11c or Ig Isotype control staining versus side light scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Data shown in this Technical Data Sheet are not lot specific.

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