Differences

This shows you the differences between two versions of the page.

--- bd_facs_symphony_a5_se [2024/01/03 13:28]
flowcytometry
+++ bd_facs_symphony_a5_se [2024/03/23 21:50] (current)
flowcytometry
@@ Line 12: / Line 12: @@
 <b>Software</b>: FACSDiva 9.6<br>
 <b>Year</b>: 2023 <br>
-<b>SN</b>:  <br>
+<b>SN</b>:R6649540104 <br>
 &nbsp <br>
 &nbsp <br>
@@ Line 36: / Line 36: @@
   * Enables both spectral unmixing and compensation workflows
 \\
-**If you need a high-throughput sampler, check the [[bd_lsr_fortessa_2|BD LSRFortessa 2]].**
+**If you need high parameter cell analysis, check the [[cytek_aurora|CYTEK Aurora]].**
-\\
-**If you need a multicolor analysis of less then 16 parameters, check also [[bd_lsr_fortessa_1|BD LSRFortessa 1]], [[bd_lsr_fortessa_2|BD LSRFortessa 2]], [[bd_lsr_fortessa_X20|BD LSRFortessa X20]] or [[bd_accuri_c6|BD Accuri C6 Plus]] instead.**
+**If you need a multicolor analysis of less then 16, 13 or 4 parameters, check also the [[bd_lsr_fortessa_X20|BD LSRFortessa X20]], the [[bd_lsr_fortessa_2|BD LSRFortessa]] or [[bd_accuri_c6|BD Accuri C6 Plus]].**
+**If you need a high-throughput sampler, check the [[bd_lsr_fortessa_2|BD LSRFortessa]] or the [[cytek_aurora|CYTEK Aurora]].**
 \\
@@ Line 48: / Line 50: @@
 ===== Suggested Fluorochrome Peak Channels =====
-{{{{:facsymphony_fluorophores.png?900|}}
+{{{{:facsymphony_fluorophores.png|}}
-{{{{:facsymphony_fluorophores_2.png?900|}}
+{{{{:facsymphony_fluorophores_2.png|}}
 ===== Useful Links when Preparing your Experiment =====

Flow Cytometry Wiki