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Furthermore in this chapter different methods and assays necessary to realize these in vitro experiments are described.
The methods and assays outlined in the chapter are typically needed during the initial analysis of mice in which the expression of a gene, keratin, or other is manipulated in skin tissue.
Unlike conventional methods and assays that have significant sensitivity and throughput limitations, the ClonePix 2 System provides a unique solution to identify and select a wide range of expression levels of endogenous GPCRs in situ.
However, more oral simulating environmental testing methods, different surface characterization methods, and more cell viability testing methods and assays must be considered for more specific results which relate more to the behavior of these dental resin composites in the oral environment.
Different methods and assays ranging from simple to advanced were carried out to prove that the enzymes have the ability to degrade wool.
Cytochemical methods and assays for carnitine acetyltransferase and KCN-insensitive palmitoyl CoA oxidation were employed to determine whether chromosome damage was associated with peroxisome proliferation.
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We generated either wildtype (control group) or Egfr f24 (experimental group) GFP clones under identical conditions (See 'Materials and methods') and assayed for FSC clone frequencies at 4, 7, and 11 days post clone induction (dpci).
Peptides structurally related to the BbKI (RPGLPVRFESPLRINIIKE-NH2) reactive site were synthesized by solid-phase method and assayed for serine proteinase activity.
Details of the analytical method and assay performance are provided in the supplementary document.
Given the method specific interferences, urinary creatinine may still vary in an method and assay specific way with between assay differences related to the composition of neonatal urine.
We used 'liquid conditioning method' and assayed on 6-cm test plates with a salt gradient made by an agar plug containing 50 m m NaCl.
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