Examples of 'background fluorescence' in a sentence
Meaning of "background fluorescence"
Background fluorescence refers to the presence of low-level fluorescent signals or emissions in a sample or environment. It is the fluorescence that is detected in the absence of any intentional or specific fluorescent labeling or staining
How to use "background fluorescence" in a sentence
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background fluorescence
Background fluorescence varies from reaction to reaction.
All values are corrected for background fluorescence.
This generates background fluorescence that degrades the image.
This fluorescence would appear as background fluorescence.
Low background fluorescence is necessary for highly sensitive detection.
All values were corrected for background fluorescence.
Background fluorescence in all cases arose primarily from the primers.
The result is an increase in background fluorescence at low temperature.
Appropriate negative controls were included to correct for background fluorescence.
There is invariably some background fluorescence in the cooling water.
Such application of pigments will help reduce background fluorescence.
Background fluorescence from wells incubated in the absence of enzyme was subtracted.
Thus there may be some degree of background fluorescence.
Background fluorescence signals produced by the fluid sample itself are insignificant.
The trace contains a certain amount of background fluorescence.
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Background fluorescence is negligible.
The quadrants were based on the upper limit of background fluorescence.
Background fluorescence was subtracted.
Unlabeled yeast cells were used to set the background fluorescence.
Subtract the predicted background fluorescence intensity during each cycle.
Isotype control antibodies are used to control for background fluorescence.
A signal test to check background fluorescence and basal fluorescence signal is performed.
Residual fiber and dust can create unwanted background fluorescence.
The very low background fluorescence level of the substrate membrane is preserved.
The use of nonfat dry milk substantially reduced background fluorescence.
A background fluorescence control was prepared by adding substrate to elastase that had been prequenched.
Cells that were not transfected are used to set the background fluorescence.
The primary concern is background fluorescence that increases linearly with time.
Unstained samples and isotype controls were included to assess background fluorescence.
Matrix effects and background fluorescence can be corrected without introducing substantial error.
Mean fluorescence intensity values after subtracting background fluorescence are shown.
Some test compounds had background fluorescence under the applied experimental conditions.
Cells from wild type animals are used to set the background fluorescence.
Background fluorescence was estimated by substituting the specific primary antibodies with specific isotype controls.
At least some of these techniques can benefit from a reduction in background fluorescence.
Early temperature cycles appeared as a background fluorescence across the bottom of the plot.
In most institutes a highly active dilution of conjugate is selected giving minimal background fluorescence.
The histogram on the left represents background fluorescence in the presence of isotype matched antibody.
These materials have excellent optical characteristics in terms of transmission and background fluorescence.
Relatively low background fluorescence generally corresponds to relatively enhanced nucleic acid detection sensitivity.
Reduced HyBeacon concentrations appear to eliminate the background fluorescence affect described above.
This can give high background fluorescence in biological assays with a resultant reduced sensitivity of detection.
Binding of a peptide was regarded positive when twice the level of background fluorescence was reached.
Background fluorescence was subtracted from all values and all data were corrected for protein contents.
Control represents cells incubated with dialyzed dye alone to assess background fluorescence.
The dotted lines in each histogram represent background fluorescence after staining with negative control antibodies.
The intensity is a measure of the strength of the fluorescence signal above the background fluorescence.
Only background fluorescence was observed with any reagent used with HSB cells.
Cells stained with primary conjugated isotype control antibodies are used to determine background fluorescence.
Background fluorescence was assessed with platelets labelled with the FITC conjugated isotype control antibody.
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The cells were examined by fluorescence light microscopy
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