Product manual
Product use, preparation, operating conditions and storage.
Fluorescence enhancement on nucleic-acid binding for isolated nucleic-acid imaging and detection in suitable samples.
Packs & quoteDimeric cyanine dyes brighten on nucleic-acid binding and generally do not enter intact cells readily. Binding can alter nucleic-acid physical properties; control the dye:nucleic-acid ratio rather than assuming DNA remains unchanged.
Image suitable DNA or nucleic-acid complexes after comparing sample state and required function before and after staining.
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.
Check nucleic-acid type, length, concentration and buffer. Calculate dilution from this product’s 1 mM stock and record the final solvent fraction. Validate permeability separately for cellular use rather than assuming access to intact cells.
Confirm nucleic-acid integrity and retain unstained material and a dye blank. Isolated nucleic acid requires no cellular fixation; validate accessibility for cells or complexes.
Match nucleic-acid input, buffer and solvent fraction while comparing dye amount and binding time using this product’s guidance. Record nucleic-acid amount and its measurement basis; equal masses of different-length nucleic acids are not equal molecule counts.
Compare bound signal and free-dye background under matched, unsaturated acquisition settings, while checking the state and required function of stained nucleic acids or complexes. Confirm composition independently rather than treating total fluorescence as covalent-labeling efficiency.
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.
This dye brightens on nucleic-acid binding, which does not establish covalent NHS or click coupling. For a covalent probe, choose a reagent matched to a modified handle.
Binding can change nucleic-acid properties. Control the dye:nucleic-acid ratio and compare integrity and downstream function with unstained material, particularly in imaging or complex studies.
They occupy different detection bands. Configure illumination, filters and detectors from the selected catalog number’s excitation/emission data and validate background and signal separately.
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