Examples of 'microtiter plate reader' in a sentence
Meaning of "microtiter plate reader"
microtiter plate reader - a device used to detect and measure biological samples in microtiter plates
How to use "microtiter plate reader" in a sentence
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microtiter plate reader
The absorbances were recorded on a microtiter plate reader.
A Spectramax Plus microtiter plate reader with monochrometer is obtained from Molecular Devices ( Sunnyvale, California ).
Fluorescence is measured on a fluorescence microtiter plate reader.
A Spectramax Plus microtiter plate reader with monochrometer was obtained from Molecular Devices ( Sunnyvale, California ).
Measure the reaction by a microtiter plate reader.
A microtiter plate reader was used to read the absorbance at 405 nm.
Fluorescence was measured on a fluorescence microtiter plate reader.
Using a kinetic microtiter plate reader ( Twinreader plus, Flow Laboratories ).
Fluorecence was quantified with a fluorescent microtiter plate reader.
Determine optical density using a microtiter plate reader set to 450 nm with correction at 570 nm.
The kinetics of color development were followed using a microtiter plate reader.
The plate is then analyzed using a microtiter plate reader set for a wavelength of 450 nm.
The signal was revealed by colorimetry and quantified using a microtiter plate reader.
Plates were read on a microtiter plate reader at 620 nm.
The amidolytic reaction taking place is continuously monitored in a microtiter plate reader.
See also
The measurement was performed on a microtiter plate reader ( Perkin Elmer Envision ).
The substrate cleavage was monitored in real time in a fluorescence microtiter plate reader.
Plate were transferred into fluorescence microtiter plate reader for kinetic analyses . Table 22.
Positive reactions gave rise to a yellow color which was quantified using a conventional microtiter plate reader.
The samples were quantified using an ELISA microtiter plate reader at an absorbance of 570 nm.
Fluorescence intensity as a function of time was measured with a Dynex MFX fluorescence microtiter plate reader.
The microtiter plate reader is set to incubate at 37 °C.
The analysis was done with the software of the microtiter plate reader.
Absorbance at 450 nm was measured with a microtiter plate reader ( Thermo Appliskan Reader ).
Light absorbance for phytase activity assay was measured using a Biotek EPOCH microtiter plate reader.
The dye signal can be measured using a conventional microtiter plate reader or spectrophotometer.
Fluorescence in each well was quantitated using a Molecular Devices microtiter plate reader.
Each microtiter plate was read on a microtiter plate reader at 450 nm.
The luminometer used in this example was LabSystems Luminoskan microtiter plate reader.
The luminescence signal was measured using the Safire 2 microtiter plate reader ( Tecan, Mannedorf, Switzerland ).
The gentamicin is quantitated by reading absorbance at 450 nm in a microtiter plate reader.
Quantitation of color development was performed using a microtiter plate reader with detection at 405 nm.
Hydrolysis is monitored quantitatively by measuring the absorption at 405 nm in a microtiter plate reader.
The formation of the dye is measured in a microtiter plate reader at 405 nm.
The signal generated was measured by reading the absorbance at 450 nm using a microtiter plate reader.
Absorbance is measured at 450 nm in a microtiter plate reader TECAN GENios ™.
Color development is measured at 492 nm using an automated microtiter plate reader.
Fluorescence for HRP-beta Gal / MUG was recorded on a fluorescence microtiter plate reader ( Dynatech Laboratories ).
The fluorescence is monitored with a FLUOROSKAN ASCENT ™ microtiter plate reader.
Product formation was monitored at 650 nm using a microtiter plate reader ( Molecular devices ).
The color signal was measured by reading absorbance at 450 nm using a microtiter plate reader.
Signal recorder in a Labsystems Luminoskan microtiter plate reader.
Immunoreactivity was quantified by measuring optical density ( O.D. ) with a microtiter plate reader.
MTT reduction was determined colorimetrically using an ELISA microtiter plate reader set at 550 nm.
After the incubation period, the plates were read at 450 nm on a microtiter plate reader.
Absorbance at 405 nm was measured in a microtiter plate reader.
The CHOP was quantitated by reading absorbance at 492 nm in a microtiter plate reader.
The absorbance at 570 nm is read in a microtiter plate reader.
The ECP was quantitated by reading absorbance at 490 nm in a microtiter plate reader.
The plate was read at 492 nm using a microtiter plate reader.
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Examples of using Microtiter
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Absorbancy is then read in a microtiter plate spectrophotometer
Microtiter plates were coated with synthetic proteins
Assays were performed in microtiter plates at room temperature
Examples of using Reader
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