BD Horizon™ Fixable Viability Stain 575V
(RUO)
Recommended Assay Procedures
Preparation
Bring FVS575V dye powder and 340 μL of fresh cell culture-grade Dimethyl Sulfoxide (DMSO; eg, Sigma D2650) to room temperature. Add 340 μL of DMSO; vortex solution well. Inspect the solution and repeat vortex until the stock dye has fully dissolved. This is the Stock Solution.
Storage
Upon arrival, store the dry dye desiccated and protected from light at -80°C until use. After reconstitution with DMSO, store the Stock Solution at -20°C in small aliquots. Do not use reconstituted dye after 90 days of storage. Please discard the dye solution after 90 days post reconstitution with DMSO.
Cytometry Requirements
Violet laser-equipped Flow Cytometers (eg, BD FACSCanto™ II, BD LSRFortessa™ or BD™ LSR II) can be used. Please note that FVS575V is also excited by the UV laser. This dye can be read out of filters commonly used for BD Horizon Brilliant Violet 605 (eg, 610/20) or Pacific Orange (eg, 575/20). Fluorescence compensation is best achieved using a sample of the cells of interest. When designing multicolor staining reagent panels, please be aware of spillover into the BD Horizon BV510 channel. Panels should be optimized to take this spillover into account. We recommend titrating the dye and using the lowest possible concentration that provides adequate resolution of live and dead populations for the cell type of interest to reduce spillover.
Procedure
Fixable Viability Stain 575V labeling of cells
1. Prepare cells for flow cytometry staining using sodium azide-free buffers.
2. Wash cells one time in sodium azide- and protein-free Dulbecco's Phosphate Buffered Saline (1× DPBS).
3. Resuspend cells at 1-10×10^6 cells/ml in sodium azide- and protein-free 1× DPBS.
4. Add 1 μL of BD Horizon Fixable Viability Stain 575V Stock Solution for each 1 ml of cell suspension (1:1000) and vortex immediately.
a. Note: We recommend titrating the dye for optimal performance, as different cell types and different applications can result in a wide degree of variability in staining.
5. Incubate the mixture for 10-15 minutes at room temperature protected from light.
a. Optional: Alternatively, incubate mixtures at 37°C for 5-7 minutes or 2-8°C for 30-60 minutes.
6. Wash cells twice with 2 ml of BD Pharmingen™ Stain Buffer (FBS) (Cat. No. 554656) or the equivalent.
7. Decant the supernatant and gently mix to disrupt the cell pellet.
8. Resuspend the cells in Stain Buffer (FBS) or equivalent.
9. Stain, fix and permeabilize cells as desired for downstream applications.
Notes:
1. Each user should determine the optimal concentrations of reagents, cells, and conditions for the assay of interest. We recommend titrating the reagent in early experiments to obtain optimal results.
2. The reactivity of the free dye is quenched by washing with buffer containing protein (eg, FBS or BSA).
3. Cells may be stained in bulk prior to freezing or staining with fluorescent antibodies.
4. BD Horizon Fixable Viability Stain 575V can be used in intracellular staining assays that require fixation with formaldehyde and permeabilization with methanol and detergents such as those used for BD Phosflow™ staining (e.g., Cat. No. 558050, BD Phosflow Perm Buffer III), intracellular cytokine staining (eg, Cat. No. 554714, BD Cytofix/Cytoperm™ Fixation/Permeablization Kit), or transcription factor staining (eg, Cat. No. 562574, BD Pharmingen Transcription Factor Buffer Set).
5. Apoptotic cells can show variable staining. We recommend co-staining with, e.g., Annexin V APC (Cat. No. 550475) or Alexa Fluor® 647 Rabbit Anti-Active Caspase-3 (Cat. No. 560626) if further analysis is desired for the apoptotic cells.
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- Alexa Fluor® is a registered trademark of Molecular Probes, Inc., Eugene, OR.
- Before staining with this reagent, please confirm that your flow cytometer is capable of exciting the fluorochrome and discriminating the resulting fluorescence.
- Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
Companion Products
BD Horizon Fixable Viability Stain 575V (FVS575V) is useful for discrimination of viable from non-viable mammalian cells in multicolor flow cytometric applications. This dye reacts with and covalently binds to cell-surface and intracellular amines. Permeable plasma cell membranes, such as those present in necrotic cells, allow for the intracellular diffusion of the dye and covalent binding to higher overall concentrations of amines than in nonpermeable live cells. Therefore, necrotic cells present in a typical in vitro assay label with higher levels of dye increasing their fluorescence intensity 10-20 fold over that of viable cells. The labeled cells can be fixed with formaldehyde for downstream decontamination, freezing and/or permeabilization and subsequent intracellular staining while maintaining stable viability stain fluorescence.
BD Horizon Fixable Viability Stain 575V is excited by the Violet laser (with an excitation maximum of 396 nm), and has a fluorescence emission maximum of 572 nm.
Danger:
Hazard statement:
Causes serious eye damage.
Precautionary statements:
Wear eye protection / face protection. Wash thoroughly after handling.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor.
Disposal:
Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
Development References (5)
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Abrams B, Diwu Z, Guryev O, et al. 3-Carboxy-6-chloro-7-hydroxycoumarin: a highly fluorescent, water-soluble violet-excitable dye for cell analysis. Anal Biochem. 2009; 386(2):262-269. (Methodology). View Reference
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Burmeister Y, Lischke T, Dahler AC, et al. ICOS controls the pool size of effector-memory and regulatory T cells. J Immunol. 2008; 180(2):774-782. (Methodology). View Reference
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Charles ED, Green RM, Marukian S, et al. Clonal expansion of immunoglobulin M+CD27+ B cells in HCV-associated mixed cryoglobulinemia. Blood. 2008; 111(3):1344-1356. (Methodology). View Reference
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Perfetto SP, Chattopadhyay PK, Lamoreaux L, et al. Amine reactive dyes: an effective tool to discriminate live and dead cells in polychromatic flow cytometry. J Immunol Methods. 2006; 313(1–2):199-208. (Methodology). View Reference
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Perfetto SP, Chattopadhyay PK, Lamoreaux L, et al. Amine-reactive dyes for dead cell discrimination in fixed samples. Curr Protoc Cytom. 9(9.34)(Methodology). View Reference
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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
