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Brand Store/BDB Bioscience/BD PharmingenTM Alexa Fluor 647 Mouse Anti-Pig CD4a
BD PharmingenTM Alexa Fluor 647 Mouse Anti-Pig CD4a
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BD PharmingenTM Alexa Fluor 647 Mouse Anti-Pig CD4a

561472 ·

BDB Bioscience · Cat: 561472

₹160 – ₹240 approx.This price excludes freight and taxes. Please RFQ to get the final price.

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Catalog No: 561472
Category: reagents
Brand: BDB Bioscience

Description

Multicolor flow cytometric analysis of CD4 expression on pig peripheral blood lymphocytes. Pig whole blood was stained simultaneously with Alexa Fluor 647 Mouse Anti-Pig CD4a antibody Cat. No. 561472 and PE Mouse Anti-Pig CD3 epsilon antibody Cat. No. 561485 . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD4a versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD4 expression on pig peripheral blood lymphocytes. Pig whole blood was stained simultaneously with Alexa Fluor 647 Mouse Anti-Pig CD4a antibody Cat. No. 561472 and PE Mouse Anti-Pig CD3 epsilon antibody Cat. No. 561485 . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD4a versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD4 expression on pig peripheral blood lymphocytes. Pig whole blood was stained simultaneously with Alexa Fluor 647 Mouse Anti-Pig CD4a antibody Cat. No. 561472 and PE Mouse Anti-Pig CD3 epsilon antibody Cat. No. 561485 . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots showing the correlated expression of CD4a versus CD3 were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.

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