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--- bd_facsaria_iiu [2017/01/18 13:48]
10.97.105.213
+++ bd_facsaria_iiu [2019/08/07 17:12]
flowcytometry
@@ Line 6: / Line 6: @@
 <a href="/facility/flowcytometry/lib/exe/fetch.php?media=aria_iiu_wiki.jpg"><img src="/facility/flowcytometry/lib/exe/fetch.php?media=aria_iiu_wiki.jpg" width=300></a>
 <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> 47222) <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>
 <b>Manufacturer</b>: <a href="http://www.bdbiosciences.com/eu/home" target="_blank">BD Biosciences</a><br>
 <b>Model</b>: FACSAria IIu<br>
+<b>Nickname</b>: "Aria 2"<br>
 <b>Software</b>: FACSDiva 6.1.3<br>
 <b>Year</b>: 2005 <br>
 <b>SN</b>: P22300027 <br>
-&nbsp <br>
-&nbsp <br>
 &nbsp <br>
 &nbsp <br>
@@ Line 20: / Line 19: @@
  <br>
 &rarr; <a href="/facility/flowcytometry/doku.php?id=bd_facsaria_iiu_usage"><img src="/facility/flowcytometry/lib/exe/fetch.php?media=chart_line.png">  BD FACSAria IIu Usage Statistics</a>
-&nbsp </p>
+&nbsp
+ <br>
+&rarr; <a href="/facility/flowcytometry/doku.php?id=bd_facsaria_iiu_repair"><img src="/facility/flowcytometry/lib/exe/fetch.php?media=repair-icon.gif" width=16> BD FACSAria IIu Repair History</a></p>
 </td>
 </tr>
 </table>
 </html>
+{{:info.gif|}} **Next Scheduled Maintenance**: August 20, 2019
+{{:info.gif|}} [[aria_iiu_contamination|Pseudomonas contamination timeline]]
 ===== System overview =====
-{{  :cell_sorting.png?0x300|}} The BD FACSAria IIu //cell sorter// is a high speed benchtop digital flow cytometer equipped with a sensitive, fixed-alignment cuvette flow cell. It has three spatially separated lasers - 407 nm, 488 nm and 633 nm. Its primary function is to analyze complex populations of cells and yield pure populations of cells meeting defined criteria. The sorter can purify samples that are simply positive and negative for a single fluorophore or as complex as multi-color samples with complex gating strategies. Sorting can be performed into two or four tubes with speeds up to 25,000 events/second. The system sorts by incorporating cells from the sample tube into a stream of sterile PBS. The stream is interrogated by the lasers at the flow cell and the system electronics keeps track of each cell as they pass through the laser and determines specific cells that meet the sort criteria. A transducer vibrates the stream and induces droplet formation, with cells in the stream being incorporated into the droplets. If a cell meets the sorting criteria and is in the last drop before the break off, the instrument will charge that drop. The charged droplet is then deflected into the proper collection tube by the charge plates. Different cell types can be sorted with the use of 70 μm, 85 μm and 100 μm nozzles. If you need a yellow-green (561 nm) laser, check the [[bd_facsaria_iii|BD FACSAria III]] instead.
+{{  :cell_sorting.png?0x300|}} The BD FACSAria IIu //cell sorter// is a high speed benchtop digital flow cytometer equipped with a sensitive, fixed-alignment cuvette flow cell. It has three spatially separated lasers - 405 nm, 488 nm and 633 nm. Its primary function is to analyze complex populations of cells and yield pure populations of cells meeting defined criteria. The sorter can purify samples that are simply positive and negative for a single fluorophore or as complex as multi-color samples with complex gating strategies. Sorting can be performed into two or four tubes with speeds up to 25,000 events/second. The system sorts by incorporating cells from the sample tube into a stream of sterile PBS. The stream is interrogated by the lasers at the flow cell and the system electronics keeps track of each cell as they pass through the laser and determines specific cells that meet the sort criteria. A transducer vibrates the stream and induces droplet formation, with cells in the stream being incorporated into the droplets. If a cell meets the sorting criteria and is in the last drop before the break off, the instrument will charge that drop. The charged droplet is then deflected into the proper collection tube by the charge plates. Different cell types can be sorted with the use of 70 μm, 85 μm and 100 μm nozzles. If you need a yellow-green (561 nm) laser, check the [[bd_facsaria_iii|BD FACSAria III]] instead.
-  * Three lasers with violet (407 nm), blue (488 nm) and red (633 nm)
+  * Three lasers with violet (405 nm), blue (488 nm) and red (633 nm)
   * Multicolor analysis of up to 10 parameters
   * 70 μm, 85 μm and 100 μm nozzles available
@@ Line 41: / Line 45: @@
 ===== Fluorophores Compatibility =====
-{{:bd_facsaria_iiu_fluorophores_wiki.png?600|}}
+{{:bd_facsaria_iiu_fluorophores_wiki.png?700|}}
+\\
+{{:aria_additional_filters.png?200|}}
+\\
+\\
+{{::bd_facsaria_iiu_405.png?700|}}
+\\
+{{::bd_facsaria_iiu_488.png?700|}}
+\\
+{{::bd_facsaria_iiu_633.png?700|}}
+===== Additional Information =====
+  * **[[prepare_samples|How to prepare samples for Flow Cytometry]]**
+  * **[[sorting_faq|What should I expect when sorting?]]**
 ===== Booking Rules =====

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