流式細胞儀設施設置於生醫所內N720室,設施內共有3台流式細胞分析儀及2台流式細胞分選儀。分析儀可提供生醫所內同仁自行操作使用;分選儀則為專人操作,並開放於院內同仁及院外人士預約無菌細胞分選服務。設施同時提供分析儀操作教育訓練、流式細胞分析課程及相關實驗設計與問題諮詢。
設施地點:生醫所新棟大樓7樓,N720室
連絡電話:02-2652-3927或02-2652-3036
E-mail:flow@ibms.sinica.edu.tw
The flow cytometry core facility, which is located in Rm. N720 at IBMS, provides 3 analyzers and 2 sorters for research application. The analyzers are self-operated and opened for colleages from Institute of Biomedical Sciences; the sorters are staff-operated and opened for colleages from Academia Sinica and off-campus researchers to reserve sterilizing cell sorting service. The core facility also provides hands-on training course of analyzers, flow cytometry lectures, and consultation about experimental designs and analytic questions of related experiments.
Location: Rm. N720, 7F, New building of Institute of Biomedical Sciences.
Phone: 02-2652-3927 or 02-2652-3036.
E-mail: flow@ibms.sinica.edu.tw
1. 流式細胞分析儀教育訓練
2. 操作細胞分選服務
3. 流式細胞分析儀維護及管理
4. 相關技術支援
5. 高內涵影像系統使用教學及維護
1. Hand-on training of flow cytometry analyzers.
2. Management of flow cytometry analyzers.
3. Operating cell sorting service.
4. Technical support
1. 流式細胞分選服務預約管理
2. 操作流式細胞分選服務
3. 流式細胞分選儀之維護管理
4. 相關技術支援
1. Operating cell sorting service.
2. Reservation management of cell sorting service.
3. Maintenance of cell sorters.
4. Technical support.
廠牌:Becton Dickinson
可用激發光波長(nm):355, 404, 488, 561, 639
螢光偵測器數:17
上樣流速(μL/min):12, 24, 36, 60, 72, 120
分析速度:70,000 events/sec
上樣方式:5mL Falcon Polystyrene tube (ref. 352052, 352054, 352235), 96 well plate, 384 well plate
操作軟體:BD FACSDiva software v6.2
廠牌:Thermo Fisher Scientific
可用激發光波長(nm):405, 488, 561, 637
螢光偵測器數:14
上樣流速(μL/min):12, 25, 100, 200, 500, 1000
分析速度:35,000 events/sec
上樣方式:eppendorff, micro tube, 5mL tube
自動上樣系統:eppendorff, 96孔盤, 384 孔盤 (標準或深底盤)
影像分析:明視野影像,不具螢光影像分析功能
鏡頭倍率:20X鏡頭 (0.45 NA)
影像解析度:0.3um/pixel
影像靈敏度:> 800nm particles
影像擷取速度:~ 6000張/秒
影像尺寸:96x96 (pixel) ~ 248x248 (pixel)
操作軟體:Attune software v5.2
廠牌:Thermo Fisher Scientific
可用激發光波長(nm):405, 488, 561, 637
螢光偵測器數:14
上樣流速(μL/min):12, 25, 100, 200, 500, 1000
分析速度:35,000 events/sec
上樣方式:eppendorff, micro tube, 5mL tube
操作軟體:Attune software v4.2
廠牌:Becton Dickinson
可用激發光波長(nm):488, 633
螢光偵測器數:6
上樣流速(μL/min):12, 60, 120
分析速度:10,000 events/sec
上樣方式:5mL Falcon Polystyrene tube (ref. 352052, 352054, 352235)
操作軟體:BD FACSDiva software v6.2
廠牌:Cytek Biosciences.
可用激發光波長(nm):355, 405, 488, 561, 640
螢光偵測器數:64
分析速度:25,000 events/sec
上樣方式:5mL tube, 15mL tube
分選方式:4向、6向、96孔盤式分選
樣本收集方式:4 way for 5mL tube, 6 way for 1.5mL Eppendorf, plate sorting
生物安全配備:客製化生物安全櫃
操作軟體:SpectroFlo CS software v1.1
廠牌:Becton Dickinson
可用激發光波長(nm):375, 404, 488, 561, 639
螢光偵測器數:15
分析速度:70,000 events/sec
上樣方式:micro tube, 5mL tube, 15mL tube
分選方式:2向、4向、盤式分選
樣本收集方式:Eppendorf, micro tube, 5mL tube, 15mL tube
6-384 well plate, slide
操作軟體:BD FACSDiva software v6.2
廠牌:Becton Dickinson
可用激發光波長(nm):488, 561, 640
螢光偵測器數:6
分析速度:20,000 events/sec
上樣方式:5mL Falcon polypropylene tube (ref.352063)
分選方式:2向、盤式分選
樣本收集方式:5mL tube, 15mL tube
6-384 well plate, slide
操作軟體:BD FACSTM software
Brand:Becton Dickinson
Available Excitation wavelength(nm):355, 404, 488, 561, 639
Available fluorescense detectors:17
Flow rate(μL/min):12, 24, 36, 60, 72, 120
Analysis speed:70,000 events/sec
Sample input:5mL Falcon Polystyrene tube (ref. 352052, 352054, 352235), 96 well plate, 384 well plate
Software:BD FACSDiva software v6.2
Brand:Thermo Fisher Scientific
Available Excitation wavelength(nm):405, 488, 561, 637
Available fluorescense detectors:14
Flow rate(μL/min):12, 25, 100, 200, 500, 1000
Analysis speed:35,000 events/sec
Sample input:eppendorff, micro tube, 5mL tube
Autosampler input: eppendorff, 96- & 384-well plate (standard & deep well)
Image type: bright-field images (no fluorescent images)
Magnification: 20X objective (0.45 NA)
Image resolution: 0.3um/pixel
Image sensitivity: > 800nm particles
Image capture rate: ~ 6000 images/sec
Image size: 96x96 (pixel) ~ 248x248 (pixel)
Software:Attune NxT software v5.2
Brand:Thermo Fisher Scientific
Available Excitation wavelength(nm):405, 488, 561, 637
Available fluorescense detectors:14
Flow rate(μL/min):12, 25, 100, 200, 500, 1000
Analysis speed:35,000 events/sec
Sample input:eppendorff, micro tube, 5mL tube
Software:Attune NxT software v4.2
Brand:Becton Dickinson
Available Excitation wavelength(nm):488, 633
Available fluorescense detectors:6
Flow rate(μL/min):12, 60, 120
Analysis speed:10,000 events/sec
Sample input:5mL Falcon Polystyrene tube (ref. 352052, 352054, 352235)
Software:BD FACSDiva software v6.2
Brand:Cytek Biosciences.
Available Excitation wavelength(nm):355, 405, 488, 561, 640
Available fluorescense detectors:64
Sorting speed:25,000 events/sec
Sample input:5mL tube, 15mL tube
Collection way:4 way for 5mL tube, 6 way for 1.5mL Eppendorf, plate sorting
Collection device:1.5mL eppendorf, 5mL tube, 96 well plate
Biosafety equipment: customized Class II (Type A2) biosafety cabinet
Software:SpectroFlo CS software v1.1
Brand:Becton Dickinson
Available Excitation wavelength(nm):375, 404, 488, 561, 639
Available fluorescense detectors:15
Sorting speed:70,000 events/sec
Sample input:micro tube, 5mL tube, 15mL tube
Collection way:2-way, 4-way, plate and slide sorting
Collection device:Eppendorf, micro tube, 5mL tube, 15mL tube
6-384 well plate, slide
Software:BD FACSDiva software v6.2
Brand:Becton Dickinson
Available Excitation wavelength(nm):488, 561, 640
Available fluorescense detectors:6
Sorting speed:20,000 events/sec
Sample input:5mL Falcon polypropylene tube (ref.352063)
Collection way:2-way、plate and slide sorting
Collection device:5mL tube, 15mL tube
6-384 well plate, slide
Software:BD FACSTM software
設施英文全名:Flow Cytometry Core Facility
計劃代碼:AS-CFII-111-212
致謝範例:
1. For cell sorting:
We thank Academia Sinica Core Facility and Innovative Instrument Project (AS-CFII-111-212) for cell sorting service.
2. For flow analysis:
We thank the flow cytometry core facility of Institute of Biomedical Sciences, Academia Sinica for analysis of flow cytometry.
The user’s publication is considered as an important KPI (Key Performance Indicators) of Core Facility. To sustain continual operation of the Core Facility, users should acknowledge the contribution of Core facility in the published papers, and inform the Core Facility with the bibliographical details of the publications (E-mail: flow@ibms.sinica.edu.tw 或 CEC@ibms.sinica.edu.tw). Each Core Facility is assigned with a project ID#, by which central academic advisory committee track the research achievements (user’s publication) for evaluating the performance of the Core Facility. The acknowledgment should include the name and the project # of the Core Facility.
The name of core facility: Flow Cytometry Core Facility
Project #: AS-CFII-111-212
Example:
1. For cell sorting:
We thank Academia Sinica Core Facility and Innovative Instrument Project (AS-CFII-111-212) for cell sorting service.
2. For flow analysis:
We thank the flow cytometry core facility of Institute of Biomedical Sciences, Academia Sinica for analysis of flow cytometry.
Q3. 需要準備多少細胞數目進行細胞分選?需要預約多少分選時段?
請先確認該機器有搭載合適的激發波長的雷射。第一次上機,請先行與管理者預約教學時間。
若您是使用FACSCanto或LSRII分析儀,請將樣本置於5mL Falcon polystyrene tube (Cat. 352052, 352054, 352235);若您是使用Attune NxT分析儀,可將樣本置於1.5-2mL eppendorf、microtube或任何5mL tube。
若您是使用FACSCanto或LSRII分析儀,建議樣本濃度為1~2x106 cells/mL;若您是使用Attune NxT分析儀,建議樣本濃度為0.5~1 x106 cells/mL。
是的。由於每次實驗樣本、試劑狀態及儀器光學校準都可能有差異,為了能正確調整儀器設定,並且在分析樣本時可精確定義陽性(positive)螢光訊號範圍,我們建議每次實驗都需要準備negative control或isotype control。若您仍有任何相關實驗設計問題,歡迎與儀器管理員討論。
是的。兩種以上螢光在分析儀中被同時偵測時,可能存在光譜重疊(spectra overlap)或螢光溢散(fluorescence spillover)問題而造成偽陽性(false positive)結果,為解決此現象,必須以單染樣本進行螢光補償(compensation)進行校正,如此才能得到正確的螢光訊號。又螢光溢散現象可能會因樣本或試劑的處理或保存狀態而改變,因此我們建議每次實驗都需要準備單染樣本。若您仍有任何相關實驗設計問題,歡迎與儀器管理員討論。
請撥打電話(2652-3927或2652-3036)與分選儀操作人員預約時間。
可以。最晚須於預約日的前一天向操作人員取消預約。未取消或當日取消者,仍將按預約時段收取費用。
Q3. 需要準備多少細胞數目進行細胞分選?需要預約多少分選時段?
沒有限制使用者準備的細胞數目,使用者可以先估算自己實驗所需的細胞數目,例如預計要分選的目標細胞群佔總細胞的10%,使用者想要回收的細胞數目為106顆細胞時,請準備2x107顆細胞來進行細胞分選,算式為2x107x10%x50%=106 (50%為進行細胞分選時預估至少有一半的回收率)。依據使用者所準備來的細胞數目,來預約細胞分選所需的時間,以2x107顆細胞來說,需要預約1小時的分選時段,以確保能完成實驗。目前本設施分選時段是以半小時(30分鐘)為一個單位,最少需預約半小時。
如果是預約FACSAria的話,最多可以同時收集4群細胞;若是預約FACSJazz的話,最多可以同時收集2群細胞。
使用者需要先將細胞樣品處理成單顆細胞懸浮液,回溶於PBS或HBSS中,內含1~2%FBS及20mM HEPES。若是樣品有特殊情況,如細胞容易聚集或是包含較多的死亡細胞,可以額外添加EDTA、DNAse或是任何適合細胞分選的緩衝液中。上機前要先將樣品過濾,避免塞機。上機細胞濃度建議調整為5~10x106顆細胞/mL。
若是預約FACSJazz進行細胞分選實驗,請將上機樣品準備在 FALCON 5mL polypropylene round-bottom tube (Cat. #352063)中。而FACSAria則可以使用任何 5mL (12x75mm)圓底管或是15mL離心管,並無限制材質及廠牌。兩台分選儀皆可使用任何 5mL (12x75mm)圓底管裝1mL培養液或是15mL離心管裝3mL培養液做為樣品收集管,無限制材質及廠牌,亦可將細胞分選於多孔盤中。
Q1. What notice should I take of before reserving analyzers?
Q2. What kind of tube should be used for sample injection?
Q3. What concentration of samples is suggested for sample preparation?
Q4. Is a negative control necessary for every experiment?
Q5. Are single stained controls essential for multi-color experiments?
Q1. How can I reserve my sorting time?
Q2. Can I cancel my reserved time?
Q3. How many cells do I need to bring? How long should I book for my cell sorting?
Q4. How many populations can I sort simultaneously?
Q5. How to prepare my cells for sorting and at what concentration?
Q6. What kind of tubes should be prepared for sample injection and collection?
Q1. What notice should I take of before reserving analyzers?
Please make sure that the analyzer you reserved was equipped the laser with correct excitation wavelength. For user of first time coming, please contact instrument manager first to reserve hands-on course.
Q2. What kind of tube should be used for sample injection?
If you use the FACSCanto and LSRII analyzers, please prepare samples in 5mL Falcon polystyrene tube (Cat. 352052, 352054, 352235); if you use the Attune NxT analyzer, samples can be prepared in 1.5-2mL Eppendorf, microtube or any 5mL tube.
Q3. What concentration of samples is suggested for sample preparation?
If you use the FACSCanto and LSRII analyzers, we suggest you to use samples with concentration of 1~2x106 cells/mL; if you use the Attune NxT analyzer, we suggest you to use samples with concentration of 0.5~1x106 cells/mL.
Q4. Is a negative control necessary for every experiment?
Yes. Due to sample and reagent condition and optical adjustment of the analyzer will be different from every time, we recommend that a negative control or isotype control is necessary in every experiment for correct adjustment of instrument setting and accurate definition of positive signal. If you still have any questions of experimental designs, please feel free to contact the instrument manager.
Q5. Are single stained controls essential for multi-color experiments?
Yes. When more than two kinds of fluorescence are detected simultaneously, spectra overlap and fluorescence spillover will be generated and cause to false positive results. To prevent both phenomena, user should prepare single stains for fluorescence compensation adjustment. Furthermore, fluorescence spillover will affected by preparation or conservation of samples and reagents, so we highly recommend that single stain controls are essential every time. If you still have any questions of experimental design, please feel free to contact the instrument manager.
Q1. How can I reserve my sorting time?
Please contact the sorter operator (2652-3927 or 2652-3036) to reserve the sorting time.
Q2. Can I cancel my reserved time?
Yes. You should cancel your reserved time at least one day earlier by contacting the sorter operator. Without cancellation or cancellation on that day will still be charged full amount of the reservation time.
Q3. How many cells do I need to bring? How long should I book for my cell sorting?
This will depend on how many cells you want to recover. For example, if the target cells you are interested in sorting are 10% of your sample and you want to recover 1 x 106 target cells, you need to prepare 2 x 107 as a starting cell number (2 x 107 x 10% x 50% = 106). It is always best to calculate the number of input cells based on the worst-case scenario of a 50% yield rate so you will be sure to have an ample number of cells to start. Generally speaking, 2 x 107 cells will take 1 hour for sorting.
Q4. How many populations can I sort simultaneously?
Up to four cell populations can be sorted simultaneously by FACSAria, and two cell populations can be sorted simultaneously by FACSJazz.
Q5. How to prepare my cells for sorting and at what concentration?
The samples for sorting must be in a single cell suspension and filtered by nylon mesh (mesh size: 35µm) before sorting to prevent clogging. The sorting buffer can be PBS or HBSS containing 1%~2% FBS and 25mM HEPES. For sticky samples or samples with high percentage of death cells, you can add 1~5mM EDTA or DNAse in sorting buffer. We recommend a concentration of 5~10x106 cells/mL for sample preparation.
Q6. What kind of tubes should be prepared for sample injection and collection?
For sample injection: If using the FACSJazz sorter, sample can only be prepared in FALCON 5mL polypropylene round-bottom tube (Cat. #352063); if using the FACSAria sorter, sample can be prepared in any 5mL (12x75mm) round-bottom tube or 15mL centrifuge tube.
For sample collection: Both two sorters can sort cells into 5mL (12x75mm) round-bottom tube, 15mL centrifuge tube, 6-384 well plates or onto slide.