Product manual
Product use, preparation, operating conditions and storage.
Covalently attach a fluorophore to DNA or RNA through chemical labeling for nucleic-acid tracking and detection-method development.
Packs & quoteLabel IT chemically labels nucleic acids covalently without requiring preintroduced amino or click handles. Extent of labeling depends on nucleic-acid quality, reagent input, salt and time; validate downstream hybridization, expression or transfection separately.
For fluorescence detection and localization of DNA or RNA after removing free reagent and checking nucleic-acid integrity.
Assess hybridization, expression or delivery for the intended use rather than selecting labeling conditions from fluorescence alone.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Use nuclease-free handling and check purity and salt. High salt can inhibit labeling; purify or exchange buffer if needed.
Use labeling buffer at 1× final concentration, keep labeling reagent below 20% of total volume and add it last.
A reference 50 µL reaction for 5 µg nucleic acid contains 5 µL labeling reagent, 5 µL 10× buffer, 5 µL nucleic acid at 1 mg/mL and 35 µL nuclease-free water.
The reference reaction is 1–3 hours at 37°C. Compare input and time for the nucleic-acid type and downstream function.
For suitable samples, use the accompanying 10 kDa ultrafiltration procedure with at least three washes. Validate retention and recovery for short fragments rather than relying on nominal cutoff alone. For absorbance quantification, choose ethanol precipitation or another validated cleanup under the accompanying procedure.
Assess recovery, nucleic-acid integrity and labeling density, then test function. Store labeled material at −20°C protected from light.
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.
Compare integrity, expression, hybridization or delivery to assess effects of processing.
Confirm that post-purification signal follows the nucleic acid rather than free dye.
Select acceptable function and low free-dye background rather than maximum total fluorescence.
Mirus Bio · Label IT Nucleic Acid Labeling Kit · ML002
Manufacturer background on direct chemical labeling of existing DNA/RNA, labeling density and purification recovery. Manufacturer catalog numbers, formulation and doses are not Qihe kit specifications; check recovery for short fragments.
Labeling density and processing can affect function. Validate hybridization, expression or transfection against an unlabeled control.
Remove free reagent as specified. Its cellular distribution and background can differ from those of labeled nucleic acid.
Use the corresponding kit conditions and signal requirements, matching nucleic-acid input and comparing downstream function.
This series chemically labels existing DNA/RNA without requiring those handles. NHS-dye and click-dye reaction procedures do not apply.
Validate retention and recovery for the length, structure and purification method. Short fragments can be lost, so check a small sample first and assess fluorescence alongside integrity and function.
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