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Characterization of food compounds in terms of promotion or inhibition of cell proliferation provides information about physiological conditions and growth rate of the cells, forming the basis for numerous in vitro assays of a specific cell response, for example interleukin secretion [ 21, 22, 27– 29].
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The practical solution is to form a large battery of diverse in vitro assays for a specific animal toxicity, such as the ToxCast strategy.
In those assays, methylation content of a specific CpG site(s) within Alu elements was detected and used to represent the methylation/demethylation level of all Alu elements.
A DNA preparation obtained from a chromatin immunoprecipitation assay using pulldown of a specific form of histone H3 was successfully amplified using the modified LM-PCR, and the amplified products could be used as probes in a fluorescence in situ hybridization analysis.
Lymphocyte transformation assay involves study of a specific immune response at 50 μM.
The methods utilized in this report could be of considerable importance in designing new small molecules to compete in vivo with specific histone modification patterns and in assaying how inhibition of a specific histone PTM binding or modifying protein would impact other histone modification abundances on a genomic scale.
DOI: http://dx.doi.org/10.7554/eLife.03970.024 A second type of experiment used in many studies to provide evidence for uptake via clathrin-independent endocytosis is to perturb the function of clathrin-coated pits, and then assay continued endocytosis of a specific protein (Doherty and McMahon, 2009; Hansen and Nichols, 2009).
We used the gentle rubbing method to obtain reflex tears from all participants, and we assayed the expression of a specific set of cytokines and chemokines in the tear samples by means of the Luminex® R-200 multiplex system (Luminex, Austin, TX, USA).
This mechanism for overcoming basic signal mediated protein retention was discovered as a result of direct binding assays showing a specific interaction between both 14-3-3 14-3-3 14-3-3subunits β-COP (O'Kelly et and 2002; Yuan ethel. 2003).
However, as urinary GAG assays are not diagnostic of a specific MPS, enzyme activity assays must be performed to confirm the diagnosis.
Bioassays are divided into four broad categories based on the type of function measured in the target cells incubated in the presence of a chemokine: a) assays which measure proliferation, b) assays of cytotoxicity, c) assays dependent on the induction of a specific cell function such as chemotaxis, and d) assays estimating the quantity of a protein induced in a target cell.
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