bd_facs_symphony_a5_se
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bd_facs_symphony_a5_se [2024/01/03 13:28] flowcytometry |
bd_facs_symphony_a5_se [2024/03/23 21:50] (current) flowcytometry |
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| <tr style="border:0px solid white;"> | <tr style="border:0px solid white;"> | ||
| <td style="border:0px solid white;"> | <td style="border:0px solid white;"> | ||
| - | <a href="/facility/flowcytometry/lib/exe/fetch.php?media=facsymphony_wiki_page.jpg"><img src="/facility/flowcytometry/lib/exe/fetch.php?media=facsymphony_wiki_page.jpg"></a> | + | <a href="/facility/flowcytometry/lib/exe/fetch.php?media=facsymphony_wiki_page.jpg"><img src="/facility/flowcytometry/lib/exe/fetch.php?media=facsymphony_wiki_page.jpg" width=300></a> |
| <td style="border:0px solid white;"> <p style="line-height:1.8"> | <td style="border:0px solid white;"> <p style="line-height:1.8"> | ||
| <b>Location</b>: <a href="/facility/flowcytometry/lib/exe/fetch.php?media=flow_cytometry_map.jpg">Room P2-A-49</a> (<img src="/facility/flowcytometry/lib/exe/fetch.php?media=telephone_icon.gif" width=15> 47224) <br> | <b>Location</b>: <a href="/facility/flowcytometry/lib/exe/fetch.php?media=flow_cytometry_map.jpg">Room P2-A-49</a> (<img src="/facility/flowcytometry/lib/exe/fetch.php?media=telephone_icon.gif" width=15> 47224) <br> | ||
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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> |
|   <br> |   <br> | ||
|   <br> |   <br> | ||
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| * Enables both spectral unmixing and compensation workflows | * 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]].** | ||
| \\ | \\ | ||
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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.1704284881.txt.gz · Last modified: 2024/01/03 13:28 by flowcytometry
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