Examples of 'n-hydroxysuccinimide ester' in a sentence
Meaning of "n-hydroxysuccinimide ester"
n-hydroxysuccinimide ester: N-hydroxysuccinimide ester is a chemical compound commonly used in bioconjugation reactions for attaching molecules together. It is often employed in chemistry and biochemistry research to modify proteins or other biomolecules through specific reactions
How to use "n-hydroxysuccinimide ester" in a sentence
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n-hydroxysuccinimide ester
In the simplest embodiments this may be an N-hydroxysuccinimide ester.
The resulting N-hydroxysuccinimide ester was used immediately for conjugation to protein.
A preferred conjugation group is the N-hydroxysuccinimide ester group.
The resulting N-hydroxysuccinimide ester will conjugate automatically to amino-groups on proteins,.
The acid was then converted to its N-hydroxysuccinimide ester.
Unreacted N-hydroxysuccinimide ester groups were deactivated by injecting ethanolamine for 3 minutes at 5 µl / min.
To this solution was added 1 mmol of N-hydroxysuccinimide ester of thiolactic acid.
Molecular assembly according to claim 2, characterized in that the heterocycle is N-hydroxysuccinimide ester.
The biotin derivative contained an N-hydroxysuccinimide ester functional group which activated it for acylation.
In a further embodiment of the present invention, the heterocycle is N-hydroxysuccinimide ester.
The non-sulfonated forms of N-hydroxysuccinimide ester conjugation reagents are not water-soluble.
In the linker used in the invention, the ester group is typically a N-hydroxysuccinimide ester group.
A similar reaction of the N-hydroxysuccinimide ester of maleimidobutanoic acid 33 ( TCI ) afforded compound 34.
For tetrahydrocannabinoid, a preferred activated drug derivative is the N-hydroxysuccinimide ester derivative of the formula,.
Eliminating the excess of maleimidobutyric acid N-hydroxysuccinimide ester from the solution of step a ;.
See also
In preferred embodiments, Y is a disulfide substituent, a maleimido, haloacetyl group, or an N-hydroxysuccinimide ester.
The cross-linking agent may for example comprise an N-hydroxysuccinimide ester function and a maleimide function.
Goat anti-rsEPCR polyclonal antibody was biotinylated with biotinamidocaproate N-hydroxysuccinimide ester using standard procedures.
The preferred acylating agent is either the N-hydroxysuccinimide ester or the acid chloride.
Preferably, the reactive ester group is an N-hydroxysuccinimide ester.
This intermediate is then transformed into the corresponding N-hydroxysuccinimide ester using dicyclocarbodiimide in dioxane.
This ester may be activated, for example as a N-hydroxysuccinimide ester.
Preferably, the cross-linking reagent contains both an N-hydroxysuccinimide ester group and a maleimide group.
Figure 6 shows the chemical structure of the monovalent N-hydroxysuccinimide ester of Cy5 ™.
For example, 6-malemeidocaproic acid and 6-maleimidocaproic acid N-hydroxysuccinimide ester can be purchased from various suppliers.
For example, antibody can be biotinylated with biotinamidocaproate N-hydroxysuccinimide ester using standard procedures.
For barbiturates, a preferred activated drug derivative is the N-hydroxysuccinimide ester derivative of the formula,.
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