Examples of 'b-galactosidase activity' in a sentence

Meaning of "b-galactosidase activity"

b-galactosidase activity: Enzyme activity related to the hydrolysis of b-galactosides, often used as a marker in molecular biology experiments to assess gene expression or protein function

How to use "b-galactosidase activity" in a sentence

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b-galactosidase activity
B-galactosidase activity was measured using a chemiluminescent assay.
The tissues were analyzed for b-galactosidase activity by a cytochemical stain.
B-galactosidase activity was confirmed in the resulting transformant.
Cytoplasmic extracts were assayed for B-galactosidase activity.
B-galactosidase activity was assessed by a chemiluminescent assay.
All luciferase activities were normalized to B-galactosidase activity.
B-galactosidase activity can be measured by one of several means.
Magnesium ions are required for optimal B-galactosidase activity.
B-galactosidase activity is determined relative to cell numbers and is in arbitrary units.
The modified fragments retain B-galactosidase activity upon complementation.
Inhibition of B-Gal expression was determined by measuring the B-galactosidase activity.
Data for B-Galactosidase activity represent total values from all cells in one well.
Production of a blue color demonstrated the presence of B-galactosidase activity.
The level of B-galactosidase activity is measured in each cell pellet.
Luciferase activity for each sample was normalized to B-galactosidase activity.

See also

Moreover, the B-galactosidase activity measured is different in the three strains.
This reduction of complementation activity is reflected as a decrease in B-galactosidase activity.
Correlation of B-galactosidase activity with fusión protein solubility and folding.
Nitrate reduction, indole formation and expression of B-galactosidase activity were assayed.
The colony colour B-galactosidase activity assay was performed by conventional procedures.
Automated colorimetric assays are also available for detection of B-galactosidase activity.
The B-galactosidase activity expressed from the respective promoter was measured.
In this plate assay no loss of B-galactosidase activity and Em resistance was detected.
B-galactosidase activity of aggR-lacZ fusión in response to different concentrations of NTZ.
All treatments were performed in triplicate, and normalized for B-galactosidase activity.
The B-galactosidase activity of the supernatant was measured by quantitating the production of fluorescein.
The cell lysates were assayed for lusiferase and B-galactosidase activity.
Graph depicting expression of B-galactosidase activity in muscle tissue after transfection in vivo.
Unfortunately, a procedure for storing solutions without losing B-galactosidase activity failed.
Cultures with low B-galactosidase activity indicate the presence of a PPARδ antagonist.
An additional element of pVenv4 is the lacZ gene that encodes B-galactosidase activity.
Addition of glucose led to repression of B-galactosidase activity to nearly the basal expression level.
Luciferase activity was detected by alphascreen technology and normalized based on B-galactosidase activity.
Clones are selected on the basis of B-galactosidase activity with Xgal and ampicillin resistance.
Subsequently, the transfected cells were assayed for luceriferase and B-galactosidase activity.
The levels of B-galactosidase activity was assayed using the Tropix kit acoording the manufacturers instructions.
Brains were processed histochemically and assessed for the presence of B-galactosidase activity.
After that, the luciferase activity and B-galactosidase activity in the cell lysis solution were measured.
Normalized luciferase values were determined by dividing the luciferase activity by the B-galactosidase activity.
Two days after transfection, cells were stained for B-galactosidase activity according to the following protocol.
The subject compound may be used as substrates for a variety of enzymes with B-galactosidase activity.
The plasmid DNAs induced varying amounts of B-galactosidase activity in the vaccinia transient expression assay.
The selected cells all expressed the LacZ gene, revealed in situ by B-galactosidase activity.
After one hour induction the B-galactosidase activity of the cells was determined through Miller 's assay.
Three days after infection, the cells were lysed and B-galactosidase activity was measured.
Induction of B-galactosidase activity was performed using the AHL analogs.
To normalize the luciferase activity, the protein concentration and the B-galactosidase activity are determined.
We measured B-galactosidase activity in blood samples by the ONPG assay.
Each luciferase activety was corrected by the transfection efficiency which was calculated from B-galactosidase activity.
Transfection efficiencies in terms of B-galactosidase activity are given in Table 2.

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Examples of using B-galactosidase
B-galactosidase activity was measured using a chemiluminescent assay
The tissues were analyzed for b-galactosidase activity by a cytochemical stain
B-galactosidase activity was confirmed in the resulting transformant
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