Product manual
Product use, preparation, operating conditions and storage.
A cell-permeant nucleic-acid stain for DNA and RNA in both live and dead cells.
Packs & quoteSYTO 9 enters intact cells and binds DNA and RNA, while also staining damaged cells. Positivity alone does not demonstrate viability. Interpret nuclear, cytoplasmic or organelle signal in the sample context.
Observe nucleic-acid-associated signal. Validate the paired dye, species and signal competition for dual-stain viability analysis.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Confirm whether the pack is solid, an mM stock or a fold-concentrated solution. Do not reconstitute an existing solution as a solid or interchange molar and fold-concentration units.
Define live or fixed preparation, check other dyes and channels, and record collection, staining and acquisition times.
Handle consistently and gently, retaining intact cells or applying suitable fixation for the objective. Do not pre-fix or permeabilize groups intended for original membrane-integrity assessment.
Use the purchased formulation and instructions for concentration/time series, comparing background, positive separation and saturation.
Set thresholds with unstained and suitable positive controls, matching acquisition settings. Include single-stain compensation or unmixing for multicolor assays.
Select a document and enter your phone and email. Include the lot number for a CoA.
Product use, preparation, operating conditions and storage.
Spectra, measurement conditions and detection settings for the exact catalog number.
Lot-specific test results. Include the lot number from the vial.
Handling, storage and emergency response information.
Establish sample autofluorescence and detection background.
Compare doses and processing steps to assess changes caused by dye, sample loss or exposure.
Thermo Fisher Scientific · Molecular Probes Handbook · Section 8.1
Distinguishes DNA preference, membrane permeability and suitable readouts among nucleic-acid stains.
SYTO 9 stains both live and dead cells; positivity alone does not establish viability.
SYTO 9 binds DNA and RNA; interpret distribution using sample nucleic acids and permeability rather than treating every green signal as a nucleus.
Dye pairing, species, cell condition and signal competition affect the result. Use known live/dead controls and validate thresholds and proportions in the actual system.
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