GIMM Flow Wiki

aria_fusion_contamination

flowcytometry — 2026-05-18T10:34:05+02:00

BD FACSAria Fusion Pseudomonas contamination 2025 Date Sheath tank Stream 03/01 ✘ ✔ 10/01 ✘ ✔ 17/01 ✘ ✔ 24/01 ✘ ✔ 31/01 ✘ ✔ 07/02 ✔ ✔

aria_iii_contamination

flowcytometry — 2026-05-18T10:33:51+02:00

BD FACSAria III Pseudomonas contamination 2025 Date Sheath tank Stream 03/01 ✔ ✔ 10/01 ✘ ✔ 17/01 ✘ ✔ 24/01 ✔ ✔ 31/01 ✘ ✔ 07/02 ✘ ✔ 14/02

s8_contamination

flowcytometry — 2026-05-18T10:33:23+02:00

BD FACSDiscover S8 Pseudomonas contamination 2025 Date Sheath tank Stream 10/01 ✘ ✔ 17/01 ✔ ✔ 24/01 ✘ ✘ 31/01 ✔ ✔ 14/02 ✔ ✔ 21/02 ✘ ✔

sop.flow.999_-_tango_remote_workstation_v2.pdf

flowcytometry — 2026-05-15T13:01:46+02:00

workstations

flowcytometry — 2026-05-15T13:00:07+02:00

Flow cytometry data analysis can be performed either on-site at the Foxtrot workstation (available to all users) or remotely (restricted to Lisbon GIMM users). In all cases, analysis is conducted within a Mambo Area, where the required software is available (see table below).

cytek_aurora_cs_contamination

flowcytometry — 2026-05-12T17:06:03+02:00

CYTEK Aurora CS Pseudomonas contamination 2025 Date Sheath tank Stream 08/01 ✘ ✘ 17/01 ✔ ✔ 23/01 ✔ ✔ 30/01 ✔ ✔ 06/02 ✔ ✔ 13/02 ✔ ✔ 20/02

aria_iiu_contamination

flowcytometry — 2026-05-12T17:04:55+02:00

BD FACSAria IIu Pseudomonas contamination 2025 Date Sheath tank Stream 08/01 ✘ ✔ 17/01 ✘ ✔ 23/01 ✘ ✔ 30/01 ✘ ✔ 06/02 ✘ ✔ 13/02 ✘ ✔ 20/02

start

flowcytometry — 2026-05-11T17:54:57+02:00

---------- ---------- ----------

bd_accuri_c6 - [Additional Information]

flowcytometry — 2026-05-11T17:47:09+02:00

System overview The BD Accuri C6 Plus cell analyzer is an easy-to-use benchtop flow cytometer that allows for absolute cell counting and has a flexible optical layout. It has two lasers - 488 nm and 640 nm and four fluorescence detectors. The BD Accuri C6 Plus can acquire up to 10,000 events/second, with the data being digitally collected over a 7-decade dynamic range. Its low pressure pumping system allows for acquisition with any type of device (e.g. FACS, Eppendorf or Falcon tubes). Since th…

trainingselfsorting

flowcytometry — 2026-05-08T15:33:07+02:00

How to become a power user We provide training in cell sorting to researchers falling into one of the following categories: * Projects involving a lot of cell sorts (1-2 x per week) for at least a couple of months. * Users who often need to sort outside of service hours (e.g. unexpected patient samples, which have to be processed immediately).

trainingspectralflow

flowcytometry — 2026-05-08T15:29:10+02:00

To use our equipments you must attend the 3 hour session on the Principles of Flow Cytometry. If you haven’t already, please book your Session. To use our Spectral Analysers and Cell Sorters, you must attend a second theoretical session on the Principles of Spectral Flow Cytometry.

trainingimagingflow

flowcytometry — 2026-05-08T15:28:12+02:00

To operate our equipment you must attend the 3 hour session on the Principles of Flow Cytometry. If you haven’t already, please book your Session. We will schedule the practical training session on the imaging cell analyser, depending on the equipment availability and the planned date of your first experiment. Ideally,

sop.ucf.049_spetroflo_cytek_aurora_tutorial_users.docx - created

flowcytometry — 2026-04-24T18:39:11+02:00

amnis_new.png

flowcytometry — 2026-04-22T16:16:28+02:00

moonwalk_workstation_new.png - created

flowcytometry — 2026-04-21T11:22:19+02:00

moonwalk_workstation_new.jpg - created

flowcytometry — 2026-04-21T11:21:00+02:00

sop.flow.996_-_mambo_remote_workstation_.pdf

flowcytometry — 2026-04-20T11:32:56+02:00

favicon.ico

flowcytometry — 2026-04-17T01:08:42+02:00

wiki:favicon.ico - created

flowcytometry — 2026-04-17T01:08:27+02:00

banner_training.png - created

flowcytometry — 2026-04-16T19:02:04+02:00