Examples of 'sulfhydryl groups' in a sentence
Meaning of "sulfhydryl groups"
sulfhydryl groups ~ chemical groups containing a sulfur atom and a hydrogen atom, commonly found in proteins and important for the structure and function of biomolecules
How to use "sulfhydryl groups" in a sentence
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sulfhydryl groups
Haloacetyls react with sulfhydryl groups at physiologic pH.
Stoichiometric percentage with respect to sulfhydryl groups.
Free sulfhydryl groups were alkylated with iodoacetic acid.
Functional groups reactive with sulfhydryl groups.
Additionally sulfhydryl groups are blocked with iodoacetic acid.
Lead has a high affinity for sulfhydryl groups.
Polypeptides lacking sulfhydryl groups can be modified by adding a cysteine residue.
Subunit structure and sulfhydryl groups.
Sulfhydryl groups can be generated by reduction of an intramolecular disulfide bond of an antibody.
It contains no sugar or free sulfhydryl groups.
The sulfhydryl groups can be sulfhydryl groups on cysteine side chains.
Thiophthalimides react with free sulfhydryl groups to form disulfides.
It is preferred to produce a conjugate having no remaining free or reactive sulfhydryl groups.
A low level of sulfhydryl groups.
Cisplatin is inactivated intracellularly and in the blood stream by sulfhydryl groups.
See also
Haloacetals can be reacted with sulfhydryl groups over a broad pH range.
The hydrogels may be substantially free of derivatized sulfhydryl groups.
Those proteins which contain sulfhydryl groups can be labeled directly.
Sulfhydryl groups can be introduced into an antibody fragment to improve radiometal binding.
The protein should not contain free sulfhydryl groups.
The oxidation of sulfhydryl groups in actomyosin is specifically catalyzed by ferrous or cupric ions.
The function of the dithiothreitol is to protect sulfhydryl groups in a protein.
Sulfhydryl groups can be introduced into a polypeptide chain to provide proximal groups.
Chemically reduced sulfhydryl groups.
Introduction of sulfhydryl groups into the protein molecule vÃa thiolation is the most used method.
An alkylating sulfhydryl reagent is added to alkylate the free sulfhydryl groups of hemoglobin.
Sulfhydryl groups may also be used as a reactive group for attachment of the dextran moiety.
Proteins which contain free sulfhydryl groups can be labeled directly.
The purified antibody is then conjugated to a drug vÃa one or more free sulfhydryl groups.
Of particular interest are substitutions of sulfhydryl groups unnecessary for biological activity.
Protein coatings can be linked to targets through side chain amino or sulfhydryl groups.
The reaction of sulfhydryl reagent with sulfhydryl groups of hemoglobin produces iodide.
Sulfhydryl groups on thiolated PerCP then reacted with disulfide groups of activated IgG molecules.
This derivative is reactive towards nucleophiles including amine and sulfhydryl groups on proteins.
The resulting protected sulfhydryl groups were exposed by reaction of the proteins with hydroxylamine hydrochloride.
Loss of activity correlates with the modification of two sulfhydryl groups per subunit.
Said sulfhydryl groups can also form disulfides with other thiols such as glutathione.
They inactivate enzymes by reacting with the sulfhydryl groups to form hemisilver sulfides.
The resulting conjugate is then reacted with peptides or proteins having free sulfhydryl groups.
The results show that the amount of sulfhydryl groups in both compartments stays constant.
Sulfhydryl groups may also be used as a reactive group for attaching the polyethylene glycol molecules.
Antibodies are reduced prior to conjugation in order to render sulfhydryl groups available for conjugation.
Sulfhydryl groups can be generated by reduction of an intramolecular disulfide bond of a Ligand.
Any solid support which specifically binds reactive sulfhydryl groups may be employed.
Sulfhydryl groups are found in cysteine, glutathione and homocysteine.
This example describes a protocol to incorporate free sulfhydryl groups into a dextran molecule.
Residual free sulfhydryl groups are capped with 4 mol.
Preferred proteolytic enzymes are those which are substantially free of sulfhydryl groups or disulfide bonds.
Each dichain has several free sulfhydryl groups that are available for drug attachment.
Preferred proteolytic enzymes are those which are substaptially free of sulfhydryl groups or disulfide bonds.
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