Examples of 'free thiol' in a sentence
Meaning of "free thiol"
free thiol: In chemistry, a free thiol refers to a sulfur-containing organic compound that has a reactive sulfur atom capable of forming bonds with other molecules or participating in chemical reactions without being bound to another sulfur atom
How to use "free thiol" in a sentence
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free thiol
Free thiol was extracted with ethyl ether.
Optional deprotection to release the free thiol.
Cysteine has a free thiol group having an antioxidative action.
Stabilized compositions of proteins having a free thiol moiety.
No free thiol was detected.
This was a maleimide that was able to react with a free thiol.
Free thiol groups are necessary for labelling scFvs with technetium.
The nanoparticles are purified from free thiol ligands by repeated extractions.
X designates a functional group capable of reacting with a free thiol radical.
The derivatised free thiol residues may be a carboxyamide or carboxymethylated derivatives.
The eluate was analyzed for concentration and free thiol content.
This suggested that recovery of the free thiol might be possible under suitable conditions.
This gel is no longer thermoreversible and no longer contains free thiol groups.
Also such compounds require a free thiol group for technetium chelation.
This polymer is now ready to conjugate with biomolecules containing a free thiol.
See also
Excess maleimide groups can be quenched by adding free thiol reagents such as mercaptoethanol.
A carrier of choice for this invention is albumin conjugated through its free thiol.
Oxygen gas can also oxidize the free thiol group into the disulfide bond.
This salt is cleaved by the addition of concentrated base to yield the free thiol.
The albumin molecule contains a natural free thiol group that is a natural antioxidant for formulation stabilization.
Mention may also be made of silanes comprising masked or free thiol functional groups.
Free thiol chemistry was used for the attachment of PEG to these residues.
The thiol modification refers to a chemical modification process of introducing free thiol groups.
Release of the free thiol of formula I.
A sample was removed from each of the control and experimental reactions for free thiol determination.
Measuring free thiol product indicative of enzymatically active Lp-PLA2 in the sample.
A thiocarbamate may be made by treating a compound containing a free thiol group with an isocyanate.
In such case, free thiol groups can be generated by reduction of native disulfide groups.
This was deemed the maximum loading possible given the free thiol content of the microcapsules.
The free thiol content was determined using Ellman 's reagent.
Disulfide content was calculated from the difference between total sulfur content and free thiol content.
In the denaturated state, a free thiol group is exposed.
The protein plus spacer is then incubated with HSA microcapsules containing free thiol groups.
The polypeptide does not contain any free thiol group ( under reducing conditions ).
The protein plus linker is then incubated with HSA microcapsules containing free thiol groups.
In embodiments, one or more free thiol groups of a PBRM are produced by reducing a protein.
NOCl is bubbled through the solution to nitrosylate the free thiol groups.
All cysteins are paired, since no free thiol groups are detected with Ellman 's test.
LiOH saponification gave the free thiol.
The amount of free thiol in a protein may be estimated by the standard Ellman 's assay.
The MPA covalently bonds to the free thiol on the albumin.
Only 7 % of free thiol was present in the purified peptide.
These interchain bonds may be converted to free thiol groups by e . g.
The free thiol containing protein is glucocerebrosidase ( GCB ).
According to the present disclosure, a preferred maytansinoid has a free thiol group.
Gly acts as a spacer, while Cys provides free thiol for immobilization on the electrode surface.
Alternatively the parent compound can be prepared from the free thiol as follows,.
N-acetylcysteine contains a free thiol group, thus, is known as an antioxidant.
The cysteine was used for site-specific PEGylation using free thiol chemistry.
Subsequently free thiol groups were blocked with 20mM Iodoacetamide.
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