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prepare_samples [2021/04/07 16:11]
flowcytometry
prepare_samples [2024/01/17 18:44] (current)
flowcytometry [How do you get started?]
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 Talk to us about your experiment! If you want to use Flow Cytometry, we can help you design your new experiment. Get in contact with us and we will guide you through the Flow Cytometry Facility, and suggest the best systems for your project. Finally, we will book a training session with you and plan a trial run with your samples. Talk to us about your experiment! If you want to use Flow Cytometry, we can help you design your new experiment. Get in contact with us and we will guide you through the Flow Cytometry Facility, and suggest the best systems for your project. Finally, we will book a training session with you and plan a trial run with your samples.
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 +Here you can find summed up information on the essentials of handling your samples. ​
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 +For more info check our **full document** on <​html><​a href="​https://​imm.medicina.ulisboa.pt/​facility/​flowcytometry/​lib/​exe/​fetch.php?​media=sop.ucf.005_-_how_to_prepare_samples_for_flow_cytometry.pdf"​ target="​_blank">​ How to prepare cell samples for Flow Cytometry</​a></​html>​.
  
  
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 {{ cell_conc_instruments_imm.jpg?​450 ​ }} {{ cell_conc_instruments_imm.jpg?​450 ​ }}
  
-In all situations, removing cell clumps, dead cells, and debris is essential to eliminate false positives and obtain results of the highest quality.\\ After getting a single-cell suspension, you should bring your cells in the right buffer, to avoid reestablishment of cell clumps. A buffer of **PBS + 2% FBS/BSA** is a good basic buffer.+In all situations, removing cell clumps, dead cells, and debris is essential to eliminate false positives and obtain results of the highest quality.\\ After getting a single-cell suspension, you should bring your cells in the right buffer, to avoid reestablishment of cell clumps. A buffer of **PBS + 2% FBS/BSA** is a good basic buffer. ​\\ 
 +Please filter all your buffers with a 0.2 µm filter to reduce bioburden and microparticulate contamination. \\
 Adding **25 mM HEPES buffer (pH 7.0)** is a good idea as well, as HEPES has better buffering properties at high pressure than PBS does.\\ You may need to add **1mM EDTA**, especially if you have adherent cells, as it helps chelate divalent cations that are often required for the formation of cell aggregates. In addition, if you have a high percentage of dead cells, adding **DNase** is strongly recommended as it reduces clumping caused by free DNA.\\ Before analysis or sorting, you should **filter your cells** through a nylon mesh. For analysis, a 70µm or 100µm mesh (BD Falcon™ cell strainers ref. 352350 and 352360) should work. For sorting, the mesh size should be inferior to the size of the nozzle: 40µm mesh for 70µm nozzle (BD Falcon™ cell strainers ref. 352340) and 70µm mesh for 85µm and 100µm nozzle. Adding **25 mM HEPES buffer (pH 7.0)** is a good idea as well, as HEPES has better buffering properties at high pressure than PBS does.\\ You may need to add **1mM EDTA**, especially if you have adherent cells, as it helps chelate divalent cations that are often required for the formation of cell aggregates. In addition, if you have a high percentage of dead cells, adding **DNase** is strongly recommended as it reduces clumping caused by free DNA.\\ Before analysis or sorting, you should **filter your cells** through a nylon mesh. For analysis, a 70µm or 100µm mesh (BD Falcon™ cell strainers ref. 352350 and 352360) should work. For sorting, the mesh size should be inferior to the size of the nozzle: 40µm mesh for 70µm nozzle (BD Falcon™ cell strainers ref. 352340) and 70µm mesh for 85µm and 100µm nozzle.
  
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 Notify us before bringing any cells of human or non-human primate origin to the core facility so we can help you assess the biosafety level of your cells. Most human primary cells and many human cell lines are BSL-2, posing hazards to laboratory staff and the environment.\\ Only BSL-1 and BSL-2 samples are allowed in the UCF room. BSL-3 and BSL-4 samples are not permitted. Notify us before bringing any cells of human or non-human primate origin to the core facility so we can help you assess the biosafety level of your cells. Most human primary cells and many human cell lines are BSL-2, posing hazards to laboratory staff and the environment.\\ Only BSL-1 and BSL-2 samples are allowed in the UCF room. BSL-3 and BSL-4 samples are not permitted.
    
-  ***Analysis of cells by flow cytometry:​** The analytical cytometers (BD LSRFortessa 1, 2X-20, BD Accuri C6 and Amnis ImageStream Mark II) are suitable for BSL-1 work only. BSL-2 cells must be fixed before use on these instruments. If your work requires analysis of unfixed BSL-2 cells, this can be done on the BD FACSAria ​III with aerosol containment. +  ***Analysis of cells by flow cytometry:​** The analytical cytometers (BD Accuri C6BD LSRFortessa ​X-20, BD FACSymphony A5 SE, CYTEK Aurora ​and Amnis ImageStream Mark II) are suitable for BSL-1 work only. BSL-2 cells must be fixed before use on these instruments. If your work requires analysis of unfixed BSL-2 cells, this can be done on the BD FACSAria ​Fusion and BD FACSymphony S6 SE with aerosol containment. 
-  ***Sorting of cells by flow cytometry:​** BSL-2 unfixed cells (e.g.human samples) may only be sorted on the BD FACSAria ​III with aerosol containment. BD FACSAria ​IIu can only sort BSL-1 and fixed BSL-2 material. For all cells of human origin, provide product sheet listing biosafety level or proof the cells.+  ***Sorting of cells by flow cytometry:​** BSL-2 unfixed cells (e.g. human samples) may only be sorted on the BD FACSAria ​Fusion and BD FACSymphony S6 SE with aerosol containment. BD FACSAria ​III can only sort BSL-1 and fixed BSL-2 material.
  
 Many staining protocols include a fixation and/or permeabilization step. However, if yours doesn’t and you need to fix your BSL-2 cells for analysis, we suggest **[[https://​imm.medicina.ulisboa.pt/​facility/​flowcytometry/​lib/​exe/​fetch.php?​media=sop.ucf.005_-_how_to_prepare_samples_for_flow_cytometry.pdf|here]]** a quick and easy PFA fixation. Many staining protocols include a fixation and/or permeabilization step. However, if yours doesn’t and you need to fix your BSL-2 cells for analysis, we suggest **[[https://​imm.medicina.ulisboa.pt/​facility/​flowcytometry/​lib/​exe/​fetch.php?​media=sop.ucf.005_-_how_to_prepare_samples_for_flow_cytometry.pdf|here]]** a quick and easy PFA fixation.
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 **__Exclude your dead cells__** **__Exclude your dead cells__**
  
-Even though you keep your cells as happy as possible, some cells can die while handling and performing staining protocols. \\ Dead cells can affect the analysis by compromising the integrity of the data by non-specifically binding antibodies. That’s why most experiments benefit from adding a viability dye, to exclude dead cells from analysis and sorting. Also this viability staining can help you evaluate and compare the cell apoptosis and necrotic stages between cell conditions.\\ There are Fixable and Non-Fixable viability dyes. You can choose the right one for your assay depending on the purpose of your analysis and the post-staining protocol that will be performed. ​For more info check our full document on **[[https://​imm.medicina.ulisboa.pt/​facility/​flowcytometry/​lib/​exe/​fetch.php?​media=sop.ucf.005_-_how_to_prepare_samples_for_flow_cytometry.pdf|How to prepare cell samples]]**.+Even though you keep your cells as happy as possible, some cells can die while handling and performing staining protocols. \\ Dead cells can affect the analysis by compromising the integrity of the data by non-specifically binding antibodies. That’s why most experiments benefit from adding a viability dye, to exclude dead cells from analysis and sorting. Also this viability staining can help you evaluate and compare the cell apoptosis and necrotic stages between cell conditions.\\ There are Fixable and Non-Fixable viability dyes. You can choose the right one for your assay depending on the purpose of your analysis and the post-staining protocol that will be performed. .
  
 **__Perform the desired cell staining__** **__Perform the desired cell staining__**
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 We need to use the **adequate nozzle** for your experiment. ​ We need to use the **adequate nozzle** for your experiment. ​
 Our sorters have the following options: ​ Our sorters have the following options: ​
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 {{  ::​nozzlesize_cells.png?​350}} {{  ::​nozzlesize_cells.png?​350}}
   *70 µm nozzle / 70 psi   *70 µm nozzle / 70 psi
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   *100 µm nozzle / 20 psi   *100 µm nozzle / 20 psi
  
-{{nozzle_drop.png?100  }}+{{stream_nozzle.png?300  }}
 **The nozzle selection depends on the size and sensibility of your cells.**\\ The most important thing to consider: cells that are fragile or easily stressed (e.g. cultured cells) need a lower pressure sort (100 µm nozzle), independently of their size. **The nozzle selection depends on the size and sensibility of your cells.**\\ The most important thing to consider: cells that are fragile or easily stressed (e.g. cultured cells) need a lower pressure sort (100 µm nozzle), independently of their size.
  
  
 The BD FACSAria sorts faster with a smaller nozzle at higher pressure - 70 µm nozzle. With this nozzle, you can sort up to 20,000 events/​second. This nozzle is a great choice for small cells that are happy in single-cell suspension (e.g., blood and bone marrow).\\ Your cells should be no more than one-third of the size of the nozzle. Therefore, if you have larger cells, they need a larger nozzle size (85 µm or 100 µm nozzle). With these nozzles, sorts are subjected to lower pressures: with the 85 µm nozzle, you can sort at 10,000 events/​second,​ and with the 100 µm nozzle you can sort up to 7,000 events/​second. ​ The BD FACSAria sorts faster with a smaller nozzle at higher pressure - 70 µm nozzle. With this nozzle, you can sort up to 20,000 events/​second. This nozzle is a great choice for small cells that are happy in single-cell suspension (e.g., blood and bone marrow).\\ Your cells should be no more than one-third of the size of the nozzle. Therefore, if you have larger cells, they need a larger nozzle size (85 µm or 100 µm nozzle). With these nozzles, sorts are subjected to lower pressures: with the 85 µm nozzle, you can sort at 10,000 events/​second,​ and with the 100 µm nozzle you can sort up to 7,000 events/​second. ​
-{{ max_cells_sorting.png?​300}}+\\ 
 +{{ max_cells_sorting.png?​360}}
  
 We normally use PBS (0.9% NaCl) in our sorters as sheath fluid. Each individual cell is sorted inside a tiny drop of this sheath fluid. If you are using the 70 µm nozzle (high pressure, faster sorting), the drops are small and you will get approximately 1 ml of sheath fluid with every 1 million sorted cells. ​ We normally use PBS (0.9% NaCl) in our sorters as sheath fluid. Each individual cell is sorted inside a tiny drop of this sheath fluid. If you are using the 70 µm nozzle (high pressure, faster sorting), the drops are small and you will get approximately 1 ml of sheath fluid with every 1 million sorted cells. ​
prepare_samples.1617804710.txt.gz · Last modified: 2021/04/07 16:11 by flowcytometry