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BD PharmingenTM APC Mouse Anti-NHP CD45

561290 ·

BDB Bioscience · Cat: 561290

₹200 – ₹300 approx.This price excludes freight and taxes. Please RFQ to get the final price.

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Catalog No: 561290
Category: reagents
Brand: BDB Bioscience

Description

Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with APC Mouse anti-NHP CD45 antibody Cat. No. 561290; right Panel or with a APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.

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