Product manual
Product use, preparation, operating conditions and storage.
Install tetrazine handles on primary-amine-bearing molecules through an NHS ester.
Packs & quoteFirst couple the NHS ester to sample amines, then use the retained tetrazine for TCO cycloaddition. Evaluate compatibility, purification and function for both steps.
Install tetrazine handles on primary-amine-bearing molecules through an NHS ester.
Verify available tetrazine after the first cleanup and include a no-TCO control.
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 solvent and tetrazine stability; do not use another tetrazine structure’s rate as this product’s specification.
Select solvent for this structure, salt form and solubility. Calculate molar inputs from its molecular weight; equal masses of different linkers are not equimolar.
Confirm the first target group and subsequent partner, then set input, pH, temperature and time for this reagent.
Confirm solvent and tetrazine stability; do not use another tetrazine structure’s rate as this product’s specification.
Remove free reagents that interfere with the next step, retain the desired handle and complete the planned pairing.
Verify available tetrazine after the first cleanup and include a no-TCO control.
Select a document and enter your phone and email. Include the lot number for a CoA.
Product use, preparation, operating conditions and storage.
Lot-specific test results. Include the lot number from the vial.
Handling, storage and emergency response information.
Compare integrity and function with an untreated aliquot from the same preparation.
Omit activation or a paired component to assess adsorption, residual reagents and nonspecific reaction.
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Distinguishes amine-reactive forms such as NHS and isothiocyanate and competing buffers; separately establish whether a nucleic-acid sample has accessible amines.
Blackman ML, Royzen M, Fox JM. · Journal of the American Chemical Society · 130(41):13518–13519 · 2008
Studies catalyst-free tetrazine–TCO cycloaddition. Rates and stability depend on substituent structure; reported kinetics are not specifications for every linker.
DOI: 10.1021/ja8053805
First couple the NHS ester to sample amines, then use the retained tetrazine for TCO cycloaddition. Evaluate compatibility, purification and function for both steps.
It is used for coupling, modification, blocking or biotin deposition. Fluorescence requires a suitable fluorophore or detection system.
Reactive ends, spacers, salt form and solubility can differ. Establish a small-scale reaction with this reagent and analyze the product.
Verify available tetrazine after the first cleanup and include a no-TCO control.
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