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Invitrogen™ SYTOX™ Deep Red Nucleic Acid Stain, for fixed/dead cells
SYTOX Deep Red Nucleic Acid Stain is a high-affinity nucleic acid stain that easily penetrates cells with compromised plasma membranes and yet does not cross the membranes of live cells.
Brand: Invitrogen™ S11380
137.28 GBP valid until 2024-11-30
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Description
With minimal cytoplasmic staining, SYTOX Deep Red stain is particularly useful in immunocytochemistry (ICC), immunohistochemistry (IHC), and immunofluorescence (IF) experiments for staining of nuclei of fixed cells. After a brief incubation with SYTOX Deep Red stain, the nucleic acids of dead or fixed cells fluoresce a bright, deep red/far red and can be detected with a CY5/Deep Red standard filter set or laser configuration.
Features of SYTOX Deep Red Nucleic Acid Stain include:
• Impermeant to live cells; permeant to dead or fixed cells
• Excitation/emission peak: 660/682 nm
• Use with Cy5 traditional filter set or 647 laser line
• Works with mammalian cells in mono layer or 3D cell culture, animal tissue, and bacteria
• Detectable with fluorescence micro¬scopes, fluorimeters, fluorescence microplate readers, and flow cytometers
SYTOX Deep Red Nucleic Acid Stain is multiplexable with blue, green, orange, red, and near IR fluorophores, when compatible fluorescent filter/laser configurations are used. SYTOX Deep Red stain shows increased fluorescence with increasing concentrations of dsDNA, but does not show much affinity for RNA or ssDNA. It has a bright initial signal and excellent photo stability in a typical imaging experiment. These properties make SYTOX Deep Red stain a simple and quantitative single-step dead/fixed cell nucleus-labeling dye for use with fluorescence micro¬scopes, fluorimeters, fluorescence microplate readers, and flow cytometers.
SYTOX Deep Red Nucleic Acid Stain had been used successfully in mono-layer cells, thin-sliced tissue, thick-sliced tissue, 3D cell cultures/spheroids, and bacteria. It is supplied at a 1 mM concentration in DMSO (∼2000X concentration). A concentration of 0.5 μM (1X) is recommended for most applications and cell types. In fluorescent imaging of various mammalian cells, a concentration range of 2.5 μM to 0.25 μM has been used. For viability testing by flow cytometry, a concentration of 1 μM to 10 nM has been used for Jurkat cells and a range of 4 μM to 0.5 μM has been used with E. coli.
Specifications
Deep Red | |
660 nm | |
Viability Assay | |
50 μL | |
Fluorescence | |
SYTOX | |
Nucleic Acid Stain |
Store in freezer at -5°C to -30°C and protect from light. | |
Cell-Permeant | |
Fluorescence Microscope | |
50 μL | |
682 nm | |
Approved for shipment on Wet or Dry Ice | |
Nucleic Acids |
For Research Use Only. Not for use in diagnostic procedures.