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Dye solutions of lipophilic carbocyanine dyes DiB, Neuro-DiO, DiI, and DiD, as well as novel near-infrared lipophilic dyes for non-toxic labeling of cytoplasmic membranes.
CellBrite® Cytoplasmic Membrane Labeling Kits can be used to label cell cytoplasmic membranes with fluorescent dyes, available in blue, green, orange, red, and near-infrared. The labeling is nontoxic and suitable for long-term tracking of cells. The dyes also can be used to stain membranes of formaldehyde-fixed cells.
The near-infrared CellBrite® NIR Cytoplasmic Membrane Dyes are unique and due to their long wavelength emission, they can be used to label cells for small animal imaging studies for non-invasive imaging of cell migration and cell homing. CellBrite® NIR Dyes have long 18-carbon hydrophobic tails and an additional water-soluble group. These unique chemical structure elements make the dyes easy to dissolve while providing highly stable cytoplasmic membrane staining, unlike traditional carbocyanine dyes like DiI, DiO, and DiR, which are often difficult to dissolve or prone to precipitation during cell staining.
Biotium’s CellBrite® Cytoplasmic Membrane Dyes are ready-to-use and can be added directly to normal culture media to uniformly label suspended or adherent cells in culture. CellBrite® Dyes allow cell populations to be marked in distinctive fluorescent colors for identification after mixing. Double labeling can identify cells that have fused or formed stable clusters.
Note: CellBrite® Dyes primarily localize to cell surface membranes shortly after staining. However, in live cells the stained membranes become internalized by endocytosis, so staining becomes primarily intracellular over the course of a few hours in culture. See “Find the Right Stain for Your Application” below, and our Membrane Staining & Imaging Tech Tip to learn more.
CellBrite® Dyes are non-toxic and stain cells very stably. They can be used to track cells for days to weeks. However, over time the dyes will be internalized by endocytosis, resulting in labeling of intracellular vesicles. A few hours after staining, the dyes will no longer outline the plasma membrane, but will be localized inside the cell. For long-term imaging of cell surfaces in culture we recommend our CellBrite® Steady Membrane Staining Kits which distribute between the cell surface and intracellular compartments, so cells retain cell surface staining over time. For long-term visualization of cell morphology in culture, our stable, non-toxic ViaFluor® SE Cell Proliferation Kits may also be a suitable alternative. ViaFluor® SE dyes covalently label cells throughout the cytoplasm and can be tracked for several days or longer by microscopy or flow cytometry. See our Tech Tip: Using ViaFluor® SE Stains for Cell Tracing and Co-Culture to learn more.
CellBrite® Dyes can be used to stain formaldehyde-fixed cells, but the staining has poor tolerance for methanol fixation or detergent permeabilization. However, permeabilizing fixed cells before staining with CellBrite® Dyes can give good results, see our Tech Tip: Combining Lipophilic Membrane Dyes with Immunofluorescence. For staining formaldehyde-fixed cells we strongly recommend using CytoLiner™ Fixed Cell Membrane Stains which offer more robust and consistent results over the CellBrite® Cytoplasmic Membrane Dyes.
For membrane stains that withstand fixation with either formaldehyde or methanol, as well as detergent permeabilization after staining, see our CellBrite® Fix Membrane Stains and MemBrite® Fix Cell Surface Staining Kits.
CellBrite® Cytoplasmic Membrane Dyes do not stain yeast or bacteria. See our Cellular Stains Table for more information on how our dyes stain various organisms.
Watch our video where Technical Applications Scientist II, Jacqueline Steenhuis PhD answers your top questions about Biotium’s various membrane stains for fluorescence microscopy.
For additional support or product recommendations, contact us at techsupport@biotium.com.
| Dye | Ex/Em | Format | Size | Catalog No. |
|---|---|---|---|---|
| CellBrite® Blue | 360/441 nm | 250 uL of Labeling Solution, 200 X in DMSO 250 uL of Cell Loading Buffer, 200X in DMSO | 50 assays | 30024 |
| CellBrite® Green | 489/506 nm | 200X in EtOH | 1 mL | 30021 |
| CellBrite® Orange | 551/569 nm | 200X in EtOH | 1 mL | 30022 |
| CellBrite® Red | 648/670 nm | 200X in EtOH | 1 mL | 30023 |
| CellBrite® NIR680 | 683/724 nm | 2 mM in DMSO* | 100 uL | 30070 |
| CellBrite® NIR750 | 748/781 nm | 2 mM in DMSO* | 100 uL | 30077 |
| CellBrite® NIR770 | 767/806 nm | 2 mM in DMSO* | 100 uL | 30078 |
| CellBrite® NIR790 | 787/820 nm | 2 mM in DMSO* | 100 uL | 30079 |
Download a list of curated CellBrite® and MemBrite® references.
Download a list of curated CellBrite® and MemBrite® references.
While CellBrite® Cytoplasmic Membrane Dyes can stain formaldehyde-fixed cells, they generally do not give good results in cryosections, possibly because the cell membrane integrity is disrupted, exposing other membrane structures to the dyes. Some customers have reported success using these dyes with vibratome sections.
CellBrite® Cytoplasmic Membrane Dyes are not suitable for membrane staining in FFPE samples as membrane lipids are extracted during the dewaxing and rehydration process. Similarly, acetone or methanol fixation of cryosections will extract lipids, leading to poor staining.
CellBrite® Fix, MemBrite® Fix, and CellBrite® Steady are recommended for use on live cells only. In fixed cells or sections they will label intracellular structures.
In some tissue types, lectins such as CF® Dye WGA Conjugates, CF® Dye Concanavalin A Conjugates, or CF® Dye PNA Conjugates may be useful for staining cell boundaries in FFPE or frozen sections. However, the staining pattern of lectins is highly dependent on cell and tissue type, so we recommend consulting the literature before trying these stains for your tissue of interest.
Alternatively, immunostaining using cell surface-specific antibodies could be done.
So far we have not found a universal plasma membrane stain for tissue sections. This is an application of interest to us and our customers, so we are working to find new solutions.
CellBrite® Cytoplasmic Membrane Dyes are too prone to aggregation to efficiently stain EVs. Some of the CellBrite® Fix, MemBrite® Fix, and CellBrite® Steady dye options have been reported for this application, however we do not recommend them. For optimal staining of exosome membranes we recommend our ExoBrite™ True EV Membrane Stains, which are novel lipophilic membrane dyes specifically designed and optimized for efficient staining of EV membranes with minimal dye aggregation. See our Extracellular Vesicle Research page for more information about our complete line of EV stains and antibodies.
Lipophilic carbocyanine dyes like CellBrite® and CellBrite® NIR Cytoplasmic Membrane Dyes can be used to stain formaldehyde-fixed cells. Fixation with methanol or other solvents is not recommended. Permeabilization with detergents after staining will extract the dyes and alter the staining pattern. However, we’ve seen good results when formaldehyde-fixed cells are permeabilized before staining with CellBrite® dyes (See Tech Tip: Combining Lipophilic Membrane Dyes with Immunofluorescence).
CellBrite® Fix, MemBrite® Fix, and CellBrite® Steady cannot be used to stain the plasma membrane of fixed samples; these dyes will primarily stain intracellular structures in cells that are already fixed.
To find the right dye for your workflow, see our Comparison of Membrane & Cell Surface Stains, or download our Membrane & Surface Stains Brochure.