EBioscience Fixable Viability D Ye EFluor 780
Page e 1 of 2 eBiosc cience Fixable Viability V Dye D eFluo or 780 Catalog Number: N 65-0 0865 Also know wn as: FVD eFluor e 780 For Rese earch Use On nly. Not for use in diagno ostic procedu ures. Product In nformation Contents: C eBios science Fixa able Viability Dye D eFluor 78 80 Catalog C Numbe er: 65-0865 Formulation: DMSO, pre-diluted to test sizze T ore at less than n or Temperature Limitation: Sto equal to -70 C e C. Protect from light and moistture. Batch Code: R Refer to vial Use By: Referr to vial Descriptio on Fixable Via ability Dye eFlu uor 780 is a viability dye thatt can be used tto irreversibly l abel dead cellss prior to cryopreserrvation, fixation and/or permea abilization proc cedures. Unlike e 7-AAD and propidium iodide e, cells labeled d with Fixable Via ability Dyes can n be washed, fiixed, permabilized, and staine ed for intracellu ular antigens w without any losss of staining inttensity of the de ead cells. Thus s, using Fixable e Viability Dyess allows dead ccells to be excluded from ana alysis when intrac cellular targets s are being stud died. Fixable Viability Dyes m may be used to label cells from m all species. ability Dye eFlu uor 780 can be b excited by th he red (633 nm m) laser line and d has a peak emission of 780 0 nm Fixable Via that can be e detected usin ng a 780/60 ban nd pass filter (e equivalent to A APC-eFluor 78 80 or APC-Alexxa Fluor 750)). Please make sure that yo our instrument is capable of detecting this dyye. For compensation, it is re ecommended to o use a sample of o the cells of in nterest stained with the Fixable Viability Dye e. If the percenttage of dead ce ells is expected d to be less tha an 5%, then it is s recommende ed to take a small aliquot of ce ells and heat th hem at 65 C for 1 minute then n immediatelly place on ice for 1 minute. After A this treatm ment, the heat-kkilled cells can be combined 1:1 with live ce ells at compensatio and then sttained with the Fixable Viabiliity Dye. Testing g at eBiosciencce suggests tha on out of most detectors is s negligible, with compensatio on out of PE-C Cyanine7 being the highest at 5%. Actual ccompensation vvalues will depend d on each inves stigator's speciific instrument, filter sets, and d PMT voltage settings. Fixable Via ability Dye eFlu uor 780 is sup pplied as a pre--diluted solutio n prepared in h high-quality, an nhydrous DMSO. It should be protected p from light and mois sture. Store at -70 C with desssicant. It may b be freeze-thaw wed up to 20 tim mes. Allow vial to t equilibrate to o room tempera ature before op pening. ons Reported Applicatio Fixable Via ability Dye eFlu uor 780 has been b reported fo or use in flow ccytometric analysis. Applicatio ons Tested Fixable Via ability Dye eFlu uor 780 has been b tested by flow cytometricc analysis of m mouse thymocyttes. Fixable Viiability Dyes are fu ully compatible e with both IC Fixation F and Pe ermeabilization Buffers and th he Foxp3/Transscription Factor Staining Bu uffer Set. This can be used att 1 μL/mL of ce ells resuspende ed at 1-10x10e e6 cells per mL in azide-free a and serum/prottein-free PBS. It is recommen nded that the co oncentration ussed be determiined by each in nvestigator for optimal perrformance in th he assay of inte erest. otes Special No Staining wiith Fixable Viab bility Dye eFluo or 780 may be e done before or after surface e staining. Cellls may be cryopreserrved after staining with Fixable e Viability Dye eFluor 780 w with no adverse e effect on stain ning intensity o of dead cells after thawing. Reference es Ulges A, Witsch W EJ, Pram manik G, Klein M, Birkner K, Bühler B U, Wassser B, Luessi F F, Stergiou N, D Dietzen S, Brüh hl TJ, Bohn T, Bü ündgen G, Kun nz H, Waisman A, Schild H, Schmitt E, Zipp F, Bopp T. Pro otein kinase CK K2 governs the e molecular decision d betwe een encephalito ogenic TH17 ce ell and Treg ce ell developmentt. Proc Natl Accad Sci U S A. 2 2016 Sep 6;113((36):10145-50. (FVD eFluor 780, 7 FC, PubM Med) Not for further f distrib bution withoutt written conse ent. Copyrightt 2016 Thermo Fisher Scientific Inc. All A rights rese erved. All trademarks are p property of Th hermo Fisher Scientiffic and its sub bsidiaries unle ess otherwise e specified. Tel: 888.999.1371 8 1 or 858.642.2 2058 Fax x: 858.642.204 46 thermo ofisher.com/e ebioscience info@e ebioscience.co om 14 March 2017 Rev. 10 0
Page e 2 of 2 eBiosc cience Fixable Viability V Dye D eFluo or 780 Catalog Number: N 65-0 0865 Also know wn as: FVD eFluor e 780 For Rese earch Use On nly. Not for use in diagno ostic procedu ures. hamn CS, Weis skopf D, da Silv va Antunes R, Havenar-Daug ghton C, Reiss SM, Brigger M M, Dan JM, Liindestam Arleh Bothwell M, M Sette A, Crottty S. A Cytokin ne-Independen nt Approach To o Identify Antige en-Specific Human Germinal Center T Follicular F Helper Cells and Rare Antigen-Spe ecific CD4 T C Cells in Blood. J Immunol. 2016 Aug 1;197(3):98 83-93. (FVD eF Fluor 780, FC, PubMed) Pollizzi KN, Sun IH, Patel CH, Lo YC, Oh O MH, Waickm man AT, Tam A AJ, Blosser RL, Wen J, Delgoffe GM, Powelll JD. Asymmetric inheritance of o mTORC1 kin nase activity du uring division diictates CD8( ) T cell differenttiation. Nat Imm munol. 2016 Jun;1 17(6):704-11. (FVD eFluor 78 80, FC, PubMe ed) W E, Molito or JA, Blueston ne JA, Bucknerr JH, Ziegler SF F. CD4 Group p 1 Innate Lym mphoid Roan F, Sttoklasek TA, Whalen Cells (ILC) Form a Functiionally Distinct ILC Subset Th hat Is Increased d in Systemic S Sclerosis. J Immunol. 2016 M Mar 1;196(5):20 051-62. (FVD eFluor e 780, FC C, PubMed) Y, Robidoux TE E, Weinstein JS S, Craft J, Swa ain SL, Marshakk-Rothstein A. IL-21 Promote es Pulmonary Brodeur TY Fibrosis thrrough the Induction of Profibrrotic CD8 T Cells. J Immuno ol. 2015 Dec 1;195(11):5251-6 60. (FVD eFluo or 780, FC, PubMed) P S K, Cyste er JG. Cutting edge: e Identifica ation of a motile e IL-17-produccing gammadelta T cell popula ation Gray EE, Suzuki in the derm mis. J Immunol. 2011 Jun 1;18 86(11):6091-5. Related Prroducts 00-5523 eB Bioscience Foxp3 F / Transcrription Factor Staining S Buffer Set 65-0863 eB Bioscience Fixable F Viability y Dye eFluor 450 65-0864 eB Bioscience Fixable F Viability y Dye eFluor 660 65-0866 eB Bioscience Fixable F Viability y Dye eFluor 506 65-0867 eB Bioscience Fixable F Viability y Dye eFluor 520 65-0868 eB Bioscience Fixable F Viability y Dye eFluor 455UV 65-2860 eB Bioscience Fixable F Viability y Dye eFluor 506/780 Samp ple Pack 88-8824 eB Bioscience In ntracellular Fixa ation & Permea abilization Bufffer Set f distrib bution withoutt written conse ent. Not for further Copyrightt 2016 Thermo Fisher Scientific Inc. All A rights rese erved. All trademarks are p property of Th hermo Fisher Scientiffic and its sub bsidiaries unle ess otherwise e specified. Tel: 888.999.1371 8 1 or 858.642.2 2058 Fax x: 858.642.204 46 thermo ofisher.com/e ebioscience info@e ebioscience.co om 14 March 2017 Rev. 10 0
Fixable Viability Dye Cell Staining Protocol Introduction Fixable Viability Dyes (FVD) are viability dyes that can be used to irreversibly label dead cells prior to cryopreservation, fixation and/or permeabilization procedures. Unlike 7-AAD and propidium iodide, cells labeled with FVD can be washed, fixed, permeabilized, and stained for intracellular antigens without any loss of staining intensity of the dead cells. Thus, using FVD allows dead cells to be excluded from analysis when intracellular targets are being studied. FVD may be used to label cells from all species. The following table summarizes the available FVD along with their optical properties: Table of Fixable Viability Dyes Catalog Number Format Excitation source (nm) Emission (nm) 65-0868 Fixable Viability Dye eFluor 455UV 350 455 65-0863 Fixable Viability Dye eFluor 450 405 450 65-0866 Fixable Viability Dye eFluor 506 405 506 65-0867 Fixable Viability Dye eFluor 520 488 522 65-0864 Fixable Viability Dye eFluor 660 633 660 65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 Sample Pack - - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and moisture. Store at less than or equal to -70 C with desiccant. They may be freeze-thawed up to 20 times. 2. Allow vial of FVD to equilibrate to room temperature before opening. 3. For the brightest staining, it is best to stain with FVD in azide- and protein-free phosphate-buffered saline (PBS). 4. Cells may be stained with FVD before or after surface staining. After staining with FVD, cells may also be cryopreserved for analysis at a later time. It is recommended that each investigator determine the optimal concentration for the assay of interest. 5. Although FVD may often be used in combination with fixation, permeabilization and intracellular staining, FVD may also be used experiments using live, unfixed cells. 6. For compensation, it is recommended to use a sample of the cells of interest stained with the FVD only. If the percentage of dead cells is expected to be less than 5%, then it is recommended to take a small aliquot of cells and heat them at 65 C for 1 minute, then immediately place on ice for 1 minute. After this treatment, the heat-killed cells can be combined 1:1 with live cells and then stained with the FVD. Alternative staining procedures (Protocols C, D, and E) 1. Protocols C, D and E are modifications for ease-of-use which may result in reduced staining intensity of the dead cells. These alternative staining protocols should be avoided if maximum staining intensity is desired. It is recommended that each investigator determine whether these protocol modifications provide sufficient staining intensity of dead cells. 2. It is possible to stain un-lysed, whole blood with FVD. See Protocol C below for details. 3. It is possible to stain in azide-free, but protein-containing PBS. This method may result in a small reduction in the staining intensity of the dead cell population. See Protocol D below for details. 4. It is possible to stain in azide- and protein-containing PBS, such as Flow Cytometry Staining Buffer (Cat. No. 00-4222). This method may result in a significant decrease in the staining intensity of the dead cell population and/or an increase in background staining of the live cell population. See Protocol D below for details. 5. It is possible to add the FVD to an antibody cocktail before addition to the cells. The FVD should spend as little time as possible in the cocktail prior to staining. It is best to use azide-free, protein containing buffer for dilution of the antibody cocktail and FVD. See Protocol E below for details. For Research Use Only. Not for use in diagnostic procedures.
Protocol A: Standard staining in tubes Materials Phosphate-buffered saline (PBS), azide- and protein-free Flow Cytometry Staining Buffer (Cat. No. 00-4222) 12x75 mm round bottom test tubes Experimental Procedure 1. Prepare cells in 12x75 mm tubes. 2. Wash cells 2 times in azide-free and protein-free PBS. 3. Resuspend cells at 1-10x106/mL in azide-free and serum/protein-free PBS. Note: For consistent staining of cells, we do not recommend staining in less than 0.5 mL. 4. Add 1 µL of FVD per 1 mL of cells and vortex immediately. 5. Incubate for 30 minutes at 2-8 C, protect from light. 6. Wash cells 1-2 times with Flow Cytometry Staining buffer or equivalent. 7. Continue with experiment, as desired. Protocol B: Staining in 96-well plates Materials Phosphate-buffered saline (PBS), azide- and protein-free Flow Cytometry Staining Buffer ( Cat. No. 00-4222) 96-well assay plates Experimental Procedure 1. Prepare cells as desired in 96-well plates. 2. Wash cells 2 times in azide-free and serum/protein-free PBS. Completely decant supernatant. 3. Prepare a working solution of the FVD by diluting it 1:1000, in azide- and serum/protein-free PBS. Make enough for 100 µL/well. For example, if you need enough for 96 wells, add 10 µL of FVD to 10 mL of PBS. 4. Add 100 µL of the working solution of the FVD to each well and mix immediately by pipetting or gentle vortexing. 5. Incubate for 30 minutes at 2-8 C, protect from light. 6. Wash cells 1-2 times with Flow Cytometry Staining buffer or equivalent. 7. Continue with experiment, as desired. Protocol C: Staining with FVD in un-lysed whole blood Materials Phosphate-buffered saline (PBS), azide- and protein-free Flow Cytometry Staining Buffer (Cat. No. 00-4222) Red blood cell lysis buffer, such as 1X RBC Lysis Buffer (Cat. No. 00-4333), 10X RBC Lysis Buffer (Multi-species) (Cat. No. 00-4300), or 1-step Fix/Lyse Solution (10X) (Cat. No. 00-5333) 12x75 mm round bottom test tubes Experimental Procedure 1. Add un-lysed whole blood to 12x75 mm tubes. 2. Add 1 µL of FVD per 100 µL of whole blood. 3. Add other surface staining antibodies after addition of the FVD. Note: Alternatively, FVD may be added directly to the surface staining antibody cocktail at 1 µL per sample to be stained. This cocktail should be made just prior to addition to whole blood samples. See Protocol E below for details. 2 Fixable Viability Dye Cell Staining Protocol
4. Incubate for 30 minutes at 2-8 C, protect from light. 5. Wash samples 1-2 times with Flow Cytometry Staining buffer. 6. Lyse red blood cells and continue with experiment, as desired. Protocol D: Staining with FVD in azide- and/or protein-containing staining buffers Materials Flow Cytometry Staining Buffer (Cat. No. 00-4222) 12x75 mm round bottom test tubes Experimental Procedure 1. Prepare cells in 12x75 mm tubes at 1-10x106/mL in Flow Cytometry Staining buffer. 2. Add 1 µL of FVD per 1 mL of cells and vortex immediately. 3. Incubate for 30 minutes at 2-8 C, protect from light. 4. Wash cells 1-2 times with Flow Cytometry Staining buffer. 5. Continue with experiment, as desired. Protocol E: Staining with FVD in an antibody cocktail Materials Phosphate-buffered saline (PBS), azide- and protein-free Flow Cytometry Staining Buffer (Cat. No. 00-4222) 12x75 mm round bottom test tubes Experimental Procedure 1. Prepare cells in 12x75 mm tubes and resuspend at 1-10x106 in 100 µL of azide- and serum/protein free PBS, as described in Protocol A, for maximum brightness. Note: If maximal brightness is not critical, cells may be resuspended in Flow Cytometry Staining buffer (as described in Protocol D). 2. Prepare desired antibody cocktail in Flow Cytometry Staining buffer. 3. Immediately prior to addition to cells, add FVD to antibody cocktail at 0.5-1 µL per sample to be stained. Mix well. 4. Add FVD/antibody cocktail to cell samples. 5. Incubate for 30 minutes at 2-8 C, protect from light. 6. Wash cells 1-2 times with Flow Cytometry Staining buffer. 7. Continue with experiment, as desired. Fixable Viability Dye Cell Staining Protocol 3
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65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
65-0865 Fixable Viability Dye eFluor 780 633 780 65-2860 Fixable Viability Dye eFluor 506/780 S ample P ck - Table 1: Table of Fixable Viability Dyes General Notes Best practices when using Fixable Viability Dyes 1. FVD are supplied as a pre-diluted solutions prepared in high-quality, anhydrous DMSO. They should be protected from light and
Business model reporting (October 2017) was the first in this series, and it established that good business model disclosure provides the foundation for the strategic report as a whole, and in particular on how the company considers risk and viability. The second report in this series was Risk and viability reporting (November 2017), which examined the key attributes of principal risk and .
Financial Viability Analysis of Government Printing Press 4 1. Government Printing Press (GPP) This report provides a financial viability analysis of the GPP based on the financial statements and records between 2004-2008 that were provided by the GPP and were verified to be correct. All these accounts have been audited by
for coronavirus (COVID-19) for people taking a coronavirus test at a GP This is an easy read guide. January 2021. 2 Contents Introduction Prepare to test Pack up your test Throat swab Get your test results Nose swab For more information Page 3 Page 6 Page Page 9 Page 11 Page 12 7 Page 14 6 5 4 3 2 1. 3 Introduction This guide comes from the Government’s Department of Health and Social Care .
