Examples of 'cytotoxicity assays' in a sentence
Meaning of "cytotoxicity assays"
cytotoxicity assays: This phrase pertains to laboratory tests or experiments designed to evaluate the toxicity levels of substances on living cells. It is frequently used in biology, pharmacology, or toxicology research to assess the impact of drugs, chemicals, or compounds on cell viability
How to use "cytotoxicity assays" in a sentence
Basic
Advanced
cytotoxicity assays
Cytotoxicity assays are performed in the following manner.
Complement mediated cytotoxicity assays may also be used.
Cytotoxicity assays were carried out as described above.
Nonspecifically conjugated switches also demonstrated batch variability in cytotoxicity assays.
Cytotoxicity assays were carried out as follows.
CTL responses can be analyzed using cytotoxicity assays described above.
All cytotoxicity assays were performed in triplicate three times.
A primary MTS assay was used to test the optimal number of cells for cytotoxicity assays.
All cytotoxicity assays were repeated at least three times in triplicate.
MTT therefore provides a colorimetric assay that can be used for either proliferation or cytotoxicity assays.
Cytotoxicity assays are performed in the respective media described above.
The transfected EC were then analysed in CIK cytotoxicity assays.
In vitro cytotoxicity assays with the cells were performed as above.
In order to measure apoptosis, cytotoxicity assays can be employed.
Cytotoxicity assays were performed in the respective media described above.
See also
The results of infectivity and cytotoxicity assays are shown in Table XV.
Cytotoxicity assays were performed in parallel with the combination experiments.
The results of infectivity and cytotoxicity assays are reported in Table XIV.
Cytotoxicity assays are performed in parallel using HeLa cells subcultured with or without PPMP.
In order to measure necrosis and apoptosis, cytotoxicity assays can be employed.
There are many cytotoxicity assays known to those of skill in the art.
In vitro toxicology tests were completed, including important cytotoxicity assays in epithelial cells.
Suitable neuroprotective and cytotoxicity assays were developed by one of the project collaborators.
Drug toxicity in target cells are evaluated using standard viability or cytotoxicity assays e . g.
Cytotoxicity assays demonstrate that soluble LIGHT can trigger apoptosis on cells expressing lymphotoxin receptor.
These antibodies were then used in the cytotoxicity assays separately, and in combinations.
Cytotoxicity assays were carried out as described in example 2.
An aliquot of cells was used to perform antibody-dependent cellular cytotoxicity assays as follows.
Cytotoxicity assays were performed 6 days as described.
These nanoparticles were characterized and tested in cytotoxicity assays and anti-leishmania activity.
Therefore, cytotoxicity assays and in vitro screening of the compounds were performed.
Cells were grown for at least 10 days following stimulation before use in cytotoxicity assays.
Cytotoxicity assays are carried out 6 days after the final stimulation.
Culture conditions were the same as for the co-culture cytotoxicity assays described above.
Also, cytotoxicity assays were performed on several types of cell line and PBMCs.
Importantly, the ADCs were highly potent and specific in in vitro cell cytotoxicity assays.
Cytotoxicity assays are usually carried out for 96 hours after addition of test compounds.
The next 14 columns show the results of cytotoxicity assays conducted on the various immunotoxins.
The blocking effect of MRG1 mAb was further demonstrated in cytotoxicity assays.
Alternative cytotoxicity assays may also be used, such as flow based cytotoxicity assays.
CEACAM1-mediated inhibition of fresh lymphocytes was tested in natural cytotoxicity assays.
Essentially, in vitro cytotoxicity assays determine acute necrotic effects by a drug causing direct cellular damage.
The TISI cells were used for peptide-mediated cytotoxicity assays.
The results of cell cytotoxicity assays are shown in Table 1.
The cytotoxic activity of CAR-expressing NK cells was measured in FACS-based cytotoxicity assays.
MTT cytotoxicity assays were carried out after cells were treated with the TMZ-POH conjugate.
Rapid colorimetric assay for cellular growth and survival, Application to proliferation and cytotoxicity assays.
Cytotoxicity assays were performed essentially as described by T. Dreier et al.
Cells were grown for at least 10 days before use in cytotoxicity assays.
Additional exemplary cytotoxicity assays include those described in Doern et al ., J Clin Microbiol.
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Examples of using Assays
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Other aPTT assays may be affected as well
Standard chromatographic and spectral assays were used
Immunoassays or neutralization assays are useful in this context
Examples of using Cytotoxicity
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Cytotoxicity of ophthalmic preservatives on human corneal epithelium
Other solvents of low cytotoxicity may be appropriate
The cytotoxicity as a function of the concentration of solvent
