Product manual
Product use, preparation, operating conditions and storage.
Install a biotin tag with a reducible disulfide onto primary-amine-bearing molecules.
Packs & quoteThe sulfo-NHS end forms an amide with an amine. A spacer disulfide can be cleaved under suitable reducing conditions. Validate capture, release or surface-labeling use for the sample.
Install a biotin tag with a reducible disulfide onto primary-amine-bearing molecules.
Assess biotin availability and reductive release separately, recording effects on sample disulfides.
Use parameters for the exact catalog number when preparing reagents, setting reagent input or calculating results. Request a lot-specific CoA for test results.
Avoid competing amines and unsuitable reductants before labeling; remove free biotin reagent before affinity detection.
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.
Avoid competing amines and unsuitable reductants before labeling; remove free biotin reagent before affinity detection.
Remove free reagents that interfere with the next step, retain the desired handle and complete the planned pairing.
Assess biotin availability and reductive release separately, recording effects on sample disulfides.
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.
Thermo Fisher Scientific
Sample preparation, free biotin and background control in biotin-affinity detection.
thermofisher.com
Distinguishes amine-reactive forms such as NHS and isothiocyanate and competing buffers; separately establish whether a nucleic-acid sample has accessible amines.
The sulfo-NHS end forms an amide with an amine. A spacer disulfide can be cleaved under suitable reducing conditions. Validate capture, release or surface-labeling use for the sample.
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.
Assess biotin availability and reductive release separately, recording effects on sample disulfides.
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