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bd_facs_symphony_a5_se [2024/01/19 15:11]
flowcytometry [System overview]
bd_facs_symphony_a5_se [2024/03/23 21:50] (current)
flowcytometry
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 <​b>​Software</​b>:​ FACSDiva 9.6<​br>​ <​b>​Software</​b>:​ FACSDiva 9.6<​br>​
 <​b>​Year</​b>:​ 2023 <br> <​b>​Year</​b>:​ 2023 <br>
-<​b>​SN</​b>: ​ <br>+<​b>​SN</​b>:​R6649540104 ​<br>
 &nbsp <br> &nbsp <br>
 &nbsp <br> &nbsp <br>
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   * Enables both spectral unmixing and compensation workflows   * Enables both spectral unmixing and compensation workflows
 \\ \\
-**If you need multicolor ​analysis ​of more than 48 parameters, check the [[cytek_aurora|CYTEK Aurora]].**+**If you need high parameter cell analysis, check the [[cytek_aurora|CYTEK Aurora]].**
  
-**If you need a high-throughput sampler, check the [[bd_lsr_fortessa_2|BD LSRFortessa ​2]] or the [[cytek_aurora|CYTEK Aurora]].**+**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 multicolor analysis of less then 48 parameters, check also the [[bd_lsr_fortessa_X20|BD LSRFortessa X20]], ​the [[bd_lsr_fortessa_2|BD LSRFortessa ​2]] 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]].**
 \\ \\
  
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 ===== Suggested Fluorochrome Peak Channels ===== ===== 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 ===== ===== Useful Links when Preparing your Experiment =====
bd_facs_symphony_a5_se.1705673500.txt.gz · Last modified: 2024/01/19 15:11 by flowcytometry