Examples of 'protein precipitation' in a sentence
Meaning of "protein precipitation"
protein precipitation - This term describes a biochemical process in which proteins are separated from a solution by causing them to aggregate or come out of solution. It often involves the addition of reagents or changes in environmental conditions to induce the precipitation of proteins, which can then be collected, purified, or analyzed for different applications
How to use "protein precipitation" in a sentence
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protein precipitation
A protein precipitation step could be included.
Oxidized samples were extracted by protein precipitation.
Protein precipitation in tea juice was done with chilled acetone.
Maintenance of the pH in this range prevented protein precipitation.
So protein precipitation was chosen finally.
An increase in absorbance is an indication of protein precipitation.
Protein precipitation analyses to assess astringency and sensorial analysis were carried out.
At extremely high salt concentrations protein precipitation will occur.
Bulk protein precipitation is significantly reduced when a process according to the present invention is employed.
Sample preparation was performed using protein precipitation with acetonitrile.
Protein precipitation was carried out by adding I mL methanol to each sample followed by mixing.
Removal of the multivalent ions prevents protein precipitation in the solution.
The protein precipitation was performed with 50 % sulphosalicylic acid.
Samples will be prepared for injection by protein precipitation with acetonitrile.
After protein precipitation the glucuronide formed was separated by high-performance liquid chromatography ( HPLC ).
See also
Dilution with isosmotic solutions minimizes protein precipitation and turbidity.
The samples after protein precipitation are analyzed by LC / MS / MS method.
Care can and must also be taken that no protein precipitation occurs.
Be carried out with a general protein precipitation procedure ( with acetone, ammonium sulfate, or polyethylenimine ).
Test compound was extracted from the plasma by an organic protein precipitation method.
In a specific embodiment, the protein precipitation step is an alcohol fractionation step.
This indicates that the mixing ratios are inadequate from protein precipitation.
Sample cleanup was achieved using protein precipitation with acetonitrile containing 0.1 % formic acid.
Then the stability of the formulations was examined by monitoring protein precipitation with naked eyes.
These stresses would tend to produce protein precipitation in the drug chamber 41, hindering accumulator performance.
This at the same time reduces the high salt concentration resulting from protein precipitation.
Plasma samples were analyzed after protein precipitation vía liquid chromatography mass spectrometry ( LC / MS ).
Plates were shaken for 2 minutes and spun down to remove protein precipitation.
Protein precipitation of the sample was carried out using cold acetone ( sample / acetone 1, 9 ).
Samples were assayed for ainoxycillin using a method based on protein precipitation with acetonitrile.
In this case, strong protein precipitation is induced, as measured by A580 see FIG.
The samples were incubated for 10 minutes followed by protein precipitation with methanol.
Protein extracts were subjected to a two stage, sequential ion exchange treatment prior to protein precipitation.
Proteins were precipitated by addition of the provided Protein Precipitation Solution and removed by centrifugation.
For every time point, a defined plasma volume is admixed with acetonitrile for protein precipitation.
Plasma samples were extracted vía protein precipitation using acetonitrile ( 3:1 ).
Fourth, digestion using proteinase K can easily be automatised as opposed to protein precipitation.
During renaturation and refolding, protein precipitation was observed.
Except hexylamine, each one of the above reagents resulted in protein precipitation.
Notably, acidification of traditional enteral formulas may also lead to protein precipitation and phase separation.
Is a flow chart of the process disclosed in FIG 3 incorporating an optional protein precipitation step.
Plasma underwent 3 stages of preparation, reduction, protein precipitation and derivatization.
The ionic strength of the solution should be maintained below 200 mM to avoid protein precipitation.
Samples were cooled to room temperature and 100 µl of protein precipitation solution was added.
In one embodiment, the first target protein enrichment step is a protein precipitation step.
FIG 2 is a flow chart of the present invention incorporating an optional protein precipitation step.
Above 72°C, a sharp increase in signal was observed because of protein precipitation ( data not shown ).
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