BD Pharmingen™ Hoechst 34580 565877

Reactivity: Human, Mouse (Tested in Development)
Application: Flow cytometry, Immunocytochemistry, Immunofluorescence, Intracellular staining (flow cytometry) (Tested During Development)
RRID: AB_2869723
Storage Buffer: Lyophilized powder
Regulatory Status: RUO
Preparation And Storage: Preparation And Storage Store at -20°C, protected from exposure to light.
Recommended Assay Procedures: Recommended Assay Procedures Preparation Bring BD Pharmingen™ Hoechst 34580 and 1 mL distilled water to room temperature. Add 1 mL of distilled water to the vial of dye and mix well to yield a 1 mg/mL solution. Inspect the solution and repeat mixing until the stock dye has fully dissolved. Storage Upon arrival, store the dry dye desiccated and protected from light at ≤ -20°C until use. After reconstitution with water, store the reconstituted dye at ≤ -20°C in small aliquots.  The reconstituted dye is stable for at least 6 months if stored as directed. Procedure Immunofluorescent Staining of Live Cells for Nuclear Visualization 1. Dilute Hoechst 34580 solution to 1-5 μg/mL in complete medium immediately prior to use. 2. Add Hoechst 34580 solution to each sample and incubate at 37°C for 30-60 minutes. The stain time required is cell type dependent. 3. Aspirate medium containing Hoechst 34580, and add BD Pharmingen™ Stain Buffer (FBS) (Cat. No. 554656) or 1× PBS. Cells may also be analyzed without washing, but this may increase background from unbound dye. 4. Proceed to immunofluorescense analysis. 5. Immunofluorescent Staining of Fixed Cells for Nuclear Visualization 1. Fix and permeabilize cells as desired. 2. Dilute Hoechst 34580 solution to 0.5-2 µg/mL in 1× PBS immediately prior to use. 3. Add Hoechst 34580 solution to each sample at least 15 minutes before analysis. 4. Proceed to immunofluorescense analysis without washing.. 5. Staining of Live Cells for DNA Content Analysis by Flow Cytometry 1. Obtain a single cell suspension. 2. Resuspend cells at 1 × 10^6 cells/mL in complete medium containing 1-10 μg/mL Hoechst 34580. Alternatively, Hoechst 34580 may be added directly to culture without pelleting if the culture cell density does not exceed 1 × 10^6 cells/mL. a. If staining at 1 × 10^7 cells/mL (eg, 1 × 10^6 cells in 100 μL), the recommended staining concentration is 5-10 μg/mL Hoechst 34580. 3. Incubate at 37°C for 15-60 minutes. a. The optimal cell density, concentration of Hoechst 34580, and stain time for DNA content analysis may vary by cell type. Assay conditions should be optimized in preliminary experiments for best results. 4. Pellet cells by centrifugation and aspirate medium containing Hoechst 34580. a. If RNA analysis (eg, RNA-seq) is to be performed after DNA content analysis is complete, wash the cells 2-3 times in serum-free buffer (eg, 1× PBS) to ensure complete removal of residual RNAse present in cell culture medium. 5. Resuspend cells in BD Pharmingen™ Stain Buffer (FBS) or 1× PBS and proceed to analysis by flow cytometry. a. If cells are to be sorted, adding Hoechst 34580 back into the analysis buffer during acquisition at the staining concentration used may prevent dye extrusion during sorting. b. Samples should be run at a low flow rate to achieve the best results. Increased flow rates may result in a higher % CV for each cell cycle compartment in the DNA histogram. c. Software packages such as ModFit LT™ (Verity Software House) or FlowJo™ (FlowJo, LLC) may be useful for deconvoluting DNA content histograms into cell cycle compartments. 6. Staining of Fixed Cells for DNA Content Analysis by Flow Cytometry 1. Obtain a single cell suspension. 2. Treat cells on ice for 30 minutes with 70-80% ice-cold ethanol. 3. Wash cells once with BD Pharmingen™ Stain Buffer (FBS). 4. Dilute Hoechst 34580 solution to 0.2-2 μg/mL in BD Pharmingen™ Stain Buffer (FBS) or 1× PBS immediately prior to use. 5. Stain cells for 15 minutes at room temperature at a cell density of 1-2 × 10^6 cells/mL. No wash is necessary prior to analysis. a. The optimal cell density and concentration of Hoechst 34580 for DNA content analysis may vary by cell type. Assay conditions should be optimized in early experiments for best results. 6. Proceed to analysis by flow cytometry. a. Samples should be run at a low flow rate to achieve the best results. Increased flow rates may result in a higher % CV for each cell cycle compartment in the DNA histogram. b. Software packages such as ModFit LT™ (Verity Software House) or FlowJo™ (FlowJo, LLC) may be useful for deconvoluting DNA content histograms into cell cycle compartments. 7. Note: Both BD Pharmingen™ Hoechst 34580 and BD Pharmingen™ Hoechst 33342 Solution (Cat. No. 561908) may be used interchangeably for most applications according to the Recommended Assay Procedure for each dye. However for DNA content analysis, Hoechst 34580 usually gives better results than Hoechst 33342 for violet laser excitation, and Hoechst 33342 usually gives better results than Hoechst 34580 for ultraviolet laser excitation.
Product Notices: Product Notices Since applications vary, each investigator should titrate the reagent to obtain optimal results. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.