Examples of 'guanidinium' in a sentence
Meaning of "guanidinium"
guanidinium (noun) - a compound that includes guanidine functional group
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- The cation derived from guanidine.
How to use "guanidinium" in a sentence
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guanidinium
Urea was found to be superior to guanidinium chloride as denaturant.
Guanidinium groups on the oligomer or peptide do not interfere.
This procedure uses an acid guanidinium thiocyanate extraction.
Guanidinium groups on the oligomers or peptide do not interfere.
A particularly preferred guanidine derivative is cocopropylenediamine guanidinium acetate.
Urea or guanidinium and subsequent renaturation.
A preferred chaotropic agent is guanidinium thiocyanate.
Dissolution in guanidinium hydrochloride followed by gradual removal of the denaturant.
Preferred terminal cationic groups are amines and guanidinium.
Preferred guanidinium halides are hexaethylguanidinium chloride and hexaethylguanidinium bromide.
Suitable catalysts include ionic species such as guanidinium salts.
Guanidinium hydroxide is now the preferred compound for many compositions.
Particularly preferred is guanidinium carbonate.
The use of guanidinium HCl denatures the proteins and may cause aberrant results.
Representative chaotropic agents include urea and guanidinium hydrochloride.
See also
Specific preferred examples of the guanidinium salt include guanidinium thiocyanate and guanidinium hydrochloride.
In this assay sodium ions are substituted with guanidinium ions.
Addition of compounds like urea or guanidinium salts has been known to solubilize proteins.
The preferred hydroxide compounds are sodium hydroxide and guanidinium hydroxide.
This lysis buffer contains guanidinium isothiocyanate to solubilize proteins and inactivate RNases and DNases.
An important modification is the incorporation of guanidinium groups into the oligomer.
Guanidinium chloride crystallizes in orthorhombic space group Pbca.
Preferred is the guanidinium ion.
Examples include Guanidinium hydrochloride and urea at the concentrations specified hereinabove.
This isolation method is based on the use of chaotropic reagent guanidinium isothiocyanate.
RNA was extracted using guanidinium thiocyanate and selectively precipitated with lithium chloride G.
It is believed the toxin has a perhydropurine nucleus in which are incorporated two guanidinium moieties.
This molecule is a molecule having two guanidinium functions and one ammonium function.
Eosinophils were lysed immediately following collection and purification in a buffer containing guanidinium isothiocyanate.
Guanidinium Salt Optionally a guanidinium salt is present.
Known extraction techniques generally use a chaotropic agent such as guanidinium to lyse the cells.
Guanidinium thiocyanate - a chemical RNase inhibitor.
The agents most frequently used for this purpose are urea and guanidinium chloride.
Guanidinium chloride; guanadine hydrochloride.
Cells were lysed and RNA extracted using guanidinium thiocyanate.
Guanidinium carbonate, guanidinium phosphate or guanidinium sulfate are particularly preferred.
RNA was extracted from the plasma using guanidinium thiocyanate.
For example, guanidinium carbonate, guanidinium sulphate and guanidinium phosphate.
Structurally, these cations resemble guanidinium cations.
As a non-limiting example, guanidinium thiocyanate may be used to precipitate mRNA.
In some embodiments, a suitable reagent is guanidinium thiocyanate.
Preferred are the guanidinium salts, and particularly preferred is guanidine thiocyanate.
In one embodiment, the chaotropic agent is a guanidinium compound.
For example, guanidinium hydrochloride and guanidinium thiocyanate may be combined.
Poly-hexamethylendiamine guanidinium chloride.
In particular, guanidinium hydrochloride and / or guanidinium thiocyanate can be used as chaotropic agent.
In one embodiment, the refolding is at an intermediate guanidinium hydrochloride concentration.
Preferably, the guanidinium is arginine and the calcium salt is calcium carbonate.
In some embodiment, the chaotropic agent is not guanidinium thiocyanate.
Particular preference is given to hexamethyl guanidinium chloride, hexaethyl guanidinium chloride and tetrabutylphosphonium chloride.
