Product manual
Product use, preparation, operating conditions and storage.
Connect primary amines and free thiols through NHS and pyridyl-disulfide groups, forming a reducible linkage.
Packs & quoteNHS first couples to an amine, then pyridyl disulfide undergoes exchange with a thiol to form a disulfide. The linkage is reduction-sensitive and differs from SMCC coupling.
Connect primary amines and free thiols through NHS and pyridyl-disulfide groups, forming a reducible linkage.
Analyze conjugation and compare stability under relevant reducing and nonreducing conditions.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Exclude residual components that reduce disulfides or compete for thiols during coupling.
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.
Exclude residual components that reduce disulfides or compete for thiols during coupling.
Remove free reagents that interfere with the next step, retain the desired handle and complete the planned pairing.
Analyze conjugation and compare stability under relevant reducing and nonreducing conditions.
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.
thermofisher.com
Distinguishes amine-reactive forms such as NHS and isothiocyanate and competing buffers; separately establish whether a nucleic-acid sample has accessible amines.
thermofisher.com
Explains thiol addition, blocking and disulfide exchange; maleimide, NEM, SPDP and Traut’s reagent have different purposes and products.
NHS first couples to an amine, then pyridyl disulfide undergoes exchange with a thiol to form a disulfide. The linkage is reduction-sensitive and differs from SMCC coupling.
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.
Analyze conjugation and compare stability under relevant reducing and nonreducing conditions.
We use cookies and third-party analytics (Microsoft Clarity, Baidu Tongji, Google Analytics) to measure traffic and improve our service. Clarity includes session recording. You may decline — core site functionality is unaffected. View privacy policy