Product manual
Product use, preparation, operating conditions and storage.
SF–DBCO couples to azide-modified proteins, nucleic acids or materials by copper-free SPAAC. Purify the azide-bearing sample before small-scale input and functional assessment.
Packs & quoteDBCO is a strained alkyne that cycloadds to an azide. Ordinary unmodified proteins lack this paired handle; residual free azide reagents can consume DBCO.
Introduce the azide and purify first, then compare coupling, background and function at matched molar inputs.
Check azide density and accessibility. Include an azide-free surface control to assess adsorption.
Assess positive signal, negative background, recovery and function of the final conjugate. Flow-cytometric gate fractions, fluorescence intensity and bleaching under continuous illumination are different endpoints and should be recorded separately.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Remove free azide modification reagents. Review sodium azide and other additives, exchanging buffer when required.
Prepare a stock using a supported solvent and check clarity after aqueous dilution. A PEG spacer or dye-family designation does not guarantee water solubility at every concentration.
Request the supported solvent, usable concentration and sample-compatibility information for the catalog number. The SF–NH2 PBS formulation and SMCC activation step do not apply to SF–DBCO, which requires an azide-bearing target.
Confirm azide modification, sample concentration and removal of free reagent.
Use a compatible buffer, compare dye input and incubation time, and record the final solvent fraction and sample appearance.
Select desalting, size-exclusion separation, dialysis or chromatography for the sample size. Remove free reagent before measuring concentration, labeling density and function. Residual free dye raises background and biases labeling-density calculations.
Combine product analysis, a no-azide control and downstream function to assess coupling and adsorption.
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 fluorescence after purification with an unmodified aliquot from the same sample to assess adsorption and free-dye carryover.
Use an unlabeled aliquot from the same preparation to assess changes in function, aggregation and recovery.
Compare a molar input series and assess signal, negative background, product recovery and function together.
Include your sample, formulation and detection method when requesting application guidance.
Debets MF, van Berkel SS, Schoffelen S, et al. · Chemical Communications · 46(1):97–99 · 2010
Reports copper-free reaction of a strained alkyne with azides and its application to enzyme PEGylation.
DOI: 10.1039/b917797c
Agard NJ, Prescher JA, Bertozzi CR. · Journal of the American Chemical Society · 126(46):15046–15047 · 2004
Introduces ring-strain-driven azide–alkyne coupling without copper, a foundational study in SPAAC bioconjugation.
DOI: 10.1021/ja044996f
Introduce azide handles first. DBCO is not a general labeling group for native amines or thiols.
DBCO–azide SPAAC does not require copper. Adding copper is not a general way to improve this reaction.
A spacer alone does not establish this. Confirm solvent and concentration for the SKU and check for aqueous precipitation or aggregation.
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